Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr1:161206280 C>T maps to NM_001077482.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr1:161206280 C>T maps to NM_001077482.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr10:133967448 C>T maps to NM_001105521.2 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr10:133967448 C>T maps to NM_001105521.2 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr11:92570935 G>A maps to ENST00000298047 P3444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr11:92570935 G>A maps to ENST00000298047 P3444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr14:23858708 G>T maps to NM_002471.3 R1291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr14:23858708 G>T maps to NM_002471.3 R1291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr15:53998199 A>T maps to NM_182758.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr15:53998199 A>T maps to NM_182758.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr16:1412528 C>T maps to NM_032520.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr16:1412528 C>T maps to NM_032520.4 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr19:10789304 C>T maps to NM_017620.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr19:10789304 C>T maps to NM_017620.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr2:55439914 C>A maps to NM_152385.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr2:55439914 C>A maps to NM_152385.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr2:73680364 A>G maps to NM_015120.4 E2236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr2:73680364 A>G maps to NM_015120.4 E2236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr22:40417569 C>T maps to NM_138435.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr22:40417569 C>T maps to NM_138435.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr3:45077082 C>T maps to NM_003278.2 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr3:45077082 C>T maps to NM_003278.2 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr5:13727708 C>T maps to NM_001369.2 E3980E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr5:13727708 C>T maps to NM_001369.2 E3980E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr7:64004765 C>T maps to NM_178558.4 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0003-01A-01D-1490-08 chr7:64004765 C>T maps to NM_178558.4 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr1:226426779 G>A maps to ENST00000366807 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr1:226426779 G>A maps to ENST00000366807 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr13:49033966 C>T maps to NM_000321.2 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr13:49033966 C>T maps to NM_000321.2 Q702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr15:73614905 C>T maps to NM_005477.2 G1176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr15:73614905 C>T maps to NM_005477.2 G1176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr16:20439126 G>A maps to NM_017888.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr16:20439126 G>A maps to NM_017888.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr16:31409189 G>A maps to ENST00000444228 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr16:31409189 G>A maps to ENST00000444228 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr17:29586048 G>A did not map to a codon.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr17:29586048 G>A did not map to a codon.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr17:56382780 C>A maps to NM_004758.2 V1800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr17:56382780 C>A maps to NM_004758.2 V1800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr17:73729693 C>T maps to NM_001005619.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr17:73729693 C>T maps to NM_001005619.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr18:20889648 C>T maps to NM_032933.4 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr18:20889648 C>T maps to NM_032933.4 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr2:201857003 C>T maps to NM_173822.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr2:201857003 C>T maps to NM_173822.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr21:31964778 C>A maps to NM_181605.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr21:31964778 C>A maps to NM_181605.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr3:58140653 T>C maps to NM_001164317.1 P2288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr3:58140653 T>C maps to NM_001164317.1 P2288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr3:148804114 C>T maps to NM_003071.3 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr3:148804114 C>T maps to NM_003071.3 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr4:129003365 A>G maps to NM_018078.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr4:129003365 A>G maps to NM_018078.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr5:140167908 G>A maps to NM_018900.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr5:140167908 G>A maps to NM_018900.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr7:148703124 G>A maps to NM_004911.4 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr7:148703124 G>A maps to NM_004911.4 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr8:17072847 A>G maps to NM_016353.4 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr8:17072847 A>G maps to NM_016353.4 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr9:139564726 C>T maps to NM_201446.1 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chr9:139564726 C>T maps to NM_201446.1 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chrX:129370451 G>A maps to NM_017666.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0033-01A-01D-1490-08 chrX:129370451 G>A maps to NM_017666.4 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:24018319 G>C did not map to a codon.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:24018319 G>C did not map to a codon.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:66083829 G>T did not map to a codon.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:66083829 G>T did not map to a codon.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:93299217 G>C did not map to a codon.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:93299217 G>C did not map to a codon.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:144816535 T>G maps to NM_001037675.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:144816535 T>G maps to NM_001037675.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:198721382 C>T maps to ENST00000271610 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:198721382 C>T maps to ENST00000271610 I1071I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:201750336 C>T maps to ENST00000367296 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:201750336 C>T maps to ENST00000367296 I521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:233395010 C>T maps to NM_014801.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr1:233395010 C>T maps to NM_014801.3 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr10:44876320 G>A maps to NM_001178134.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr10:44876320 G>A maps to NM_001178134.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr12:662978 G>A maps to NM_173593.3 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr12:662978 G>A maps to NM_173593.3 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr12:7294682 G>A maps to NM_014718.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr12:7294682 G>A maps to NM_014718.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr12:12247836 G>A maps to NM_138722.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr12:12247836 G>A maps to NM_138722.1 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr15:40512941 G>A maps to ENST00000412359 G1059G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr15:40512941 G>A maps to ENST00000412359 G1059G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr16:1478503 C>T maps to NM_001010878.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr16:1478503 C>T maps to NM_001010878.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr17:38122550 C>T maps to NM_178171.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr17:38122550 C>T maps to NM_178171.4 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr2:113588107 G>A maps to NM_000576.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr2:113588107 G>A maps to NM_000576.2 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr2:227886827 C>T maps to ENST00000396625 A1384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr2:227886827 C>T maps to ENST00000396625 A1384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr22:38369501 T>G maps to NM_006941.3 *467Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr22:38369501 T>G maps to NM_006941.3 *467Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr22:50719358 C>T maps to NM_012401.2 E1269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr22:50719358 C>T maps to NM_012401.2 E1269E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr4:175180975 C>A maps to NM_012180.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr4:175180975 C>A maps to NM_012180.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr5:74041589 T>C maps to NM_032380.3 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr5:74041589 T>C maps to NM_032380.3 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr6:54791194 T>C maps to NM_001010872.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr6:54791194 T>C maps to NM_001010872.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr8:66963844 C>T maps to NM_033105.4 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chr8:66963844 C>T maps to NM_033105.4 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chrX:41075439 C>T maps to NM_001039590.2 Q1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0047-01A-01D-1490-08 chrX:41075439 C>T maps to NM_001039590.2 Q1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr1:158912122 G>A maps to NM_152501.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr1:158912122 G>A maps to NM_152501.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr1:248263033 C>T maps to NM_175911.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr1:248263033 C>T maps to NM_175911.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr11:4661586 C>T maps to NM_001004751.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr11:4661586 C>T maps to NM_001004751.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr12:5842029 A>G did not map to a codon.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr12:5842029 A>G did not map to a codon.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr12:117768966 C>T did not map to a codon.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr12:117768966 C>T did not map to a codon.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr16:84270707 C>T maps to NM_172347.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr16:84270707 C>T maps to NM_172347.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr17:74936836 G>A maps to NM_198955.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr17:74936836 G>A maps to NM_198955.1 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr19:43376197 C>A did not map to a codon.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr19:43376197 C>A did not map to a codon.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr20:11900454 C>G maps to NM_014962.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr20:11900454 C>G maps to NM_014962.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr20:29960754 C>T maps to NM_054112.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr20:29960754 C>T maps to NM_054112.2 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr21:31864263 G>A maps to NM_181609.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr21:31864263 G>A maps to NM_181609.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr3:14905721 G>A maps to NM_152536.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr3:14905721 G>A maps to NM_152536.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr4:1209829 G>A maps to NM_001328.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr4:1209829 G>A maps to NM_001328.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr4:126373450 G>A maps to NM_024582.4 T3760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr4:126373450 G>A maps to NM_024582.4 T3760T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr5:61887490 T>A maps to NM_001134779.1 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr5:61887490 T>A maps to NM_001134779.1 T930T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr6:149795610 C>A maps to NM_207360.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr6:149795610 C>A maps to NM_207360.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr7:143807247 C>T maps to NM_001005480.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr7:143807247 C>T maps to NM_001005480.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr8:99044504 T>C maps to ENST00000254898 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chr8:99044504 T>C maps to ENST00000254898 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:47102905 C>T maps to NM_004651.3 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:47102905 C>T maps to NM_004651.3 Y608Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:71424938 C>T maps to NM_017669.2 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:71424938 C>T maps to NM_017669.2 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:79286009 C>T maps to NM_016954.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:79286009 C>T maps to NM_016954.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:119394751 A>G maps to NM_017938.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:119394751 A>G maps to NM_017938.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:153880613 T>C maps to NM_020994.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-0055-01A-01D-1490-08 chrX:153880613 T>C maps to NM_020994.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr1:31658175 T>C did not map to a codon.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr1:31658175 T>C did not map to a codon.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr10:17735225 A>G maps to NM_003473.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr10:17735225 A>G maps to NM_003473.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr11:102272677 A>G maps to NM_052932.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr11:102272677 A>G maps to NM_052932.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr14:101201217 C>T maps to NM_003836.5 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr14:101201217 C>T maps to NM_003836.5 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr15:43552355 C>T maps to NM_201631.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr15:43552355 C>T maps to NM_201631.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr15:89056198 G>A maps to NM_017996.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr15:89056198 G>A maps to NM_017996.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr16:31368587 C>T maps to NM_000887.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr16:31368587 C>T maps to NM_000887.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr18:44560402 T>C maps to NM_016427.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr18:44560402 T>C maps to NM_016427.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr19:3730052 C>T maps to NM_014428.1 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr19:3730052 C>T maps to NM_014428.1 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr19:36340037 C>T maps to NM_004646.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr19:36340037 C>T maps to NM_004646.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr2:27303033 C>T maps to NM_007046.3 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr2:27303033 C>T maps to NM_007046.3 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr2:102638707 C>T maps to NM_004633.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr2:102638707 C>T maps to NM_004633.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr2:220012492 G>A maps to NM_024782.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr2:220012492 G>A maps to NM_024782.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr3:111264247 C>T maps to NM_198196.2 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr3:111264247 C>T maps to NM_198196.2 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr4:96761885 C>T maps to NM_005390.4 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr4:96761885 C>T maps to NM_005390.4 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr4:100349052 G>A maps to NM_000673.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr4:100349052 G>A maps to NM_000673.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr4:155157376 T>C maps to NM_017639.3 V2354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr4:155157376 T>C maps to NM_017639.3 V2354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr5:37480064 T>G maps to NM_018034.2 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr5:37480064 T>G maps to NM_018034.2 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr6:17837204 C>T maps to NM_022113.4 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr6:17837204 C>T maps to NM_022113.4 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr7:45932659 C>T maps to NM_000596.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr7:45932659 C>T maps to NM_000596.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr7:139726105 C>T maps to NM_022750.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr7:139726105 C>T maps to NM_022750.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr1:28800111 G>A maps to NM_023923.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr1:28800111 G>A maps to NM_023923.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr11:100863380 G>T maps to NM_032021.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr11:100863380 G>T maps to NM_032021.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr12:10962584 A>T maps to NM_023917.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr12:10962584 A>T maps to NM_023917.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr12:51685542 C>T maps to NM_016293.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr12:51685542 C>T maps to NM_016293.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr12:57648756 A>C maps to ENST00000438036 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr12:57648756 A>C maps to ENST00000438036 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr18:9124947 C>T maps to NM_021074.4 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr18:9124947 C>T maps to NM_021074.4 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr19:5211662 C>T maps to NM_002850.3 L1724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr19:5211662 C>T maps to NM_002850.3 L1724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr19:18331287 G>A maps to NM_000923.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr19:18331287 G>A maps to NM_000923.3 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr2:54857157 C>A maps to NM_003128.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr2:54857157 C>A maps to NM_003128.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr22:41564739 A>G maps to NM_001429.3 G1347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr22:41564739 A>G maps to NM_001429.3 G1347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr3:367747 G>A did not map to a codon.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr3:367747 G>A did not map to a codon.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr3:171426552 T>C maps to NM_002662.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr3:171426552 T>C maps to NM_002662.3 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr4:44176992 G>T maps to NM_198353.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr4:44176992 G>T maps to NM_198353.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr5:36048993 T>C maps to NM_174914.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr5:36048993 T>C maps to NM_174914.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr7:82532012 G>A maps to NM_033026.5 H4494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr7:82532012 G>A maps to NM_033026.5 H4494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr8:101153143 T>G maps to NM_001029860.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr8:101153143 T>G maps to NM_001029860.3 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr8:104337554 A>G maps to NM_003506.3 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr8:104337554 A>G maps to NM_003506.3 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr9:99084299 G>A maps to NM_007001.2 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2483-01A-01D-1494-08 chr9:99084299 G>A maps to NM_007001.2 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr14:74008215 C>G maps to NM_001037161.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr14:74008215 C>G maps to NM_001037161.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr15:86838559 G>A maps to NM_152336.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr15:86838559 G>A maps to NM_152336.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr16:20548635 G>A maps to NM_182617.3 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr16:20548635 G>A maps to NM_182617.3 R560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr16:24366256 C>T maps to NM_006539.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr16:24366256 C>T maps to NM_006539.3 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr19:19756293 C>T maps to NM_020410.2 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr19:19756293 C>T maps to NM_020410.2 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr19:23927493 T>C maps to NM_138286.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr19:23927493 T>C maps to NM_138286.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:197863058 A>G did not map to a codon.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:197863058 A>G did not map to a codon.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:226446957 C>A maps to NM_020864.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:226446957 C>A maps to NM_020864.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:226446978 C>T maps to NM_020864.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:226446978 C>T maps to NM_020864.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:238249200 G>A maps to NM_004369.3 F2786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr2:238249200 G>A maps to NM_004369.3 F2786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr20:61299252 C>T maps to NM_016354.3 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr20:61299252 C>T maps to NM_016354.3 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr22:44692616 G>A maps to NM_001099294.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr22:44692616 G>A maps to NM_001099294.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr3:3076349 C>T maps to NM_175607.1 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr3:3076349 C>T maps to NM_175607.1 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr3:15512053 G>A maps to NM_005677.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr3:15512053 G>A maps to NM_005677.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr5:137781274 G>A maps to ENST00000378339 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr5:137781274 G>A maps to ENST00000378339 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr5:140257258 G>A maps to NM_018903.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr5:140257258 G>A maps to NM_018903.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr6:7583890 G>A maps to NM_004415.2 G2132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr6:7583890 G>A maps to NM_004415.2 G2132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr6:15520427 C>T maps to NM_004973.2 P1229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr6:15520427 C>T maps to NM_004973.2 P1229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr7:30492357 G>A maps to NM_006092.2 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr7:30492357 G>A maps to NM_006092.2 D225D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr9:286570 C>T maps to NM_203447.3 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr9:286570 C>T maps to NM_203447.3 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr9:100227271 C>A maps to NM_014290.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2485-01A-01D-1494-08 chr9:100227271 C>A maps to NM_014290.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr1:22216488 G>A maps to NM_005529.5 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr1:22216488 G>A maps to NM_005529.5 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr11:6807032 C>G maps to NM_001004489.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr11:6807032 C>G maps to NM_001004489.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr11:65655865 G>A maps to NM_198897.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr11:65655865 G>A maps to NM_198897.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr11:102663438 C>T maps to NM_002421.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr11:102663438 C>T maps to NM_002421.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr12:100166858 G>A maps to NM_152788.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr12:100166858 G>A maps to NM_152788.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr15:92663773 A>C maps to NM_013272.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr15:92663773 A>C maps to NM_013272.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr17:40458320 C>T maps to NM_003152.3 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr17:40458320 C>T maps to NM_003152.3 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr19:50411933 G>A maps to NM_012346.4 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr19:50411933 G>A maps to NM_012346.4 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr3:42906815 G>A maps to NM_001296.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr3:42906815 G>A maps to NM_001296.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr3:48463527 G>A maps to NM_001130082.1 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr3:48463527 G>A maps to NM_001130082.1 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr4:40800850 G>T maps to NM_024677.4 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr4:40800850 G>T maps to NM_024677.4 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr5:55206409 C>T maps to NM_139017.4 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr5:55206409 C>T maps to NM_139017.4 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr6:100062049 G>A maps to ENST00000359773 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr6:100062049 G>A maps to ENST00000359773 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr6:107391830 G>A maps to NM_001080450.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr6:107391830 G>A maps to NM_001080450.2 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr6:138612911 C>T maps to NM_020340.4 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr6:138612911 C>T maps to NM_020340.4 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr7:150699007 C>T maps to NM_000603.4 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr7:150699007 C>T maps to NM_000603.4 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr8:21608206 G>A maps to NM_001495.4 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chr8:21608206 G>A maps to NM_001495.4 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chrX:16142186 G>A maps to NM_005314.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2486-01A-01D-1494-08 chrX:16142186 G>A maps to NM_005314.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr1:55266545 C>T maps to NM_001114108.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr1:55266545 C>T maps to NM_001114108.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr11:55653245 G>A maps to NM_032681.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr11:55653245 G>A maps to NM_032681.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr12:31255359 G>T did not map to a codon.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr12:31255359 G>T did not map to a codon.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr12:123200282 G>A maps to NM_006018.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr12:123200282 G>A maps to NM_006018.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:27613997 T>C maps to NM_020772.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:27613997 T>C maps to NM_020772.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:34073180 G>A maps to NM_139285.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:34073180 G>A maps to NM_139285.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:72878744 C>T maps to ENST00000310226 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:72878744 C>T maps to ENST00000310226 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:78195494 C>T maps to NM_173626.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr17:78195494 C>T maps to NM_173626.3 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr19:17436027 G>A maps to NM_020959.2 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr19:17436027 G>A maps to NM_020959.2 S943S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-06-0119-01A-08D-1490-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-06-0119-01A-08D-1490-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr20:48129690 G>A maps to NM_000961.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr20:48129690 G>A maps to NM_000961.3 R378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr22:46657005 G>A maps to NM_006071.1 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr22:46657005 G>A maps to NM_006071.1 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr5:5262846 C>T maps to NM_139056.2 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr5:5262846 C>T maps to NM_139056.2 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr5:140627257 G>A maps to NM_018935.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr5:140627257 G>A maps to NM_018935.2 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr6:75840566 C>T did not map to a codon.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr6:75840566 C>T did not map to a codon.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr6:128134888 G>A maps to NM_001164685.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr6:128134888 G>A maps to NM_001164685.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr7:83016343 G>A maps to NM_012431.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr7:83016343 G>A maps to NM_012431.2 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr8:27301728 C>T maps to NM_004103.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr8:27301728 C>T maps to NM_004103.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr8:79590914 G>A did not map to a codon.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chr8:79590914 G>A did not map to a codon.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chrX:34148877 C>T maps to NM_203408.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0119-01A-08D-1490-08 chrX:34148877 C>T maps to NM_203408.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr1:28362073 C>T maps to NM_001990.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr1:28362073 C>T maps to NM_001990.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr1:161138220 G>T did not map to a codon.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr1:161138220 G>T did not map to a codon.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:800588 G>A maps to NM_145886.3 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:800588 G>A maps to NM_145886.3 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:6023919 G>A maps to NM_001005179.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:6023919 G>A maps to NM_001005179.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:22747845 G>A maps to NM_005256.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:22747845 G>A maps to NM_005256.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:48286014 C>T maps to NM_001004726.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:48286014 C>T maps to NM_001004726.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:82571018 C>T maps to NM_199418.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:82571018 C>T maps to NM_199418.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:129751719 G>C maps to NM_006165.3 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr11:129751719 G>C maps to NM_006165.3 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr12:101336193 C>T maps to ENST00000392977 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr12:101336193 C>T maps to ENST00000392977 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr12:120599820 C>T maps to NM_006836.1 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr12:120599820 C>T maps to NM_006836.1 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr14:38061526 G>A maps to NM_004496.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr14:38061526 G>A maps to NM_004496.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr16:3642833 G>A maps to NM_032444.2 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr16:3642833 G>A maps to NM_032444.2 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr16:89351278 C>T maps to NM_013275.4 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr16:89351278 C>T maps to NM_013275.4 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr17:39535344 G>A maps to NM_021013.3 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr17:39535344 G>A maps to NM_021013.3 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr17:73125016 C>T maps to NM_024585.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr17:73125016 C>T maps to NM_024585.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:9213119 G>C maps to NM_001005193.1 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:9213119 G>C maps to NM_001005193.1 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:18779532 C>T maps to NM_018316.1 Y442Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:18779532 C>T maps to NM_018316.1 Y442Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:44933155 G>A maps to NM_014518.2 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:44933155 G>A maps to NM_014518.2 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:50926143 G>A maps to NM_003121.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:50926143 G>A maps to NM_003121.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:58423431 C>T maps to NM_152475.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr19:58423431 C>T maps to NM_152475.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:37516577 G>C maps to NM_005813.3 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:37516577 G>C maps to NM_005813.3 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:179597776 G>A maps to NM_133378.4 L4132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:179597776 G>A maps to NM_133378.4 L4132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:219920561 G>A maps to NM_002181.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:219920561 G>A maps to NM_002181.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:220396798 G>C maps to NM_018674.4 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:220396798 G>C maps to NM_018674.4 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:233710564 T>C maps to ENST00000373566 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:233710564 T>C maps to ENST00000373566 L1165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:234602271 C>T maps to NM_001072.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr2:234602271 C>T maps to NM_001072.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:30584452 C>T maps to NM_001011718.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:30584452 C>T maps to NM_001011718.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:36869818 G>C maps to NM_001029864.1 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:36869818 G>C maps to NM_001029864.1 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:44506780 C>G maps to NM_080752.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:44506780 C>G maps to NM_080752.3 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:51871856 C>T maps to NM_173485.5 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr20:51871856 C>T maps to NM_173485.5 H620H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr3:186917653 G>A maps to NM_153708.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr3:186917653 G>A maps to NM_153708.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr6:159206602 C>A maps to NM_001111077.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr6:159206602 C>A maps to NM_001111077.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr7:147259315 C>T maps to NM_014141.5 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chr7:147259315 C>T maps to NM_014141.5 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:49142411 C>G maps to NM_033215.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:49142411 C>G maps to NM_033215.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:69262196 G>A maps to NM_001002254.1 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:69262196 G>A maps to NM_001002254.1 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:86873002 C>T maps to NM_057162.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:86873002 C>T maps to NM_057162.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:103349046 C>T maps to NM_001012755.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0122-01A-01D-1490-08 chrX:103349046 C>T maps to NM_001012755.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:21014369 G>A maps to NM_020816.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:21014369 G>A maps to NM_020816.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:42744222 C>T maps to NM_001198850.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:42744222 C>T maps to NM_001198850.1 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:117159062 C>T maps to NM_001542.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:117159062 C>T maps to NM_001542.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:169698773 G>A maps to NM_000450.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr1:169698773 G>A maps to NM_000450.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr10:35819171 G>A did not map to a codon.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr10:35819171 G>A did not map to a codon.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr11:1642999 C>T maps to ENST00000359229 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr11:1642999 C>T maps to ENST00000359229 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr11:118074266 G>A maps to NM_001098526.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr11:118074266 G>A maps to NM_001098526.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr17:3779600 G>A maps to ENST00000381771 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr17:3779600 G>A maps to ENST00000381771 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr17:29662001 C>T maps to NM_001042492.2 Q1987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr17:29662001 C>T maps to NM_001042492.2 Q1987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr19:39591968 C>T maps to NM_001004318.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr19:39591968 C>T maps to NM_001004318.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr2:21239330 G>A maps to NM_000384.2 V1104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr2:21239330 G>A maps to NM_000384.2 V1104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr2:71058941 C>G maps to NM_015717.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr2:71058941 C>G maps to NM_015717.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr22:18274038 C>A maps to NM_015241.2 L1893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr22:18274038 C>A maps to NM_015241.2 L1893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr22:42458929 C>G maps to NM_000262.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr22:42458929 C>G maps to NM_000262.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr4:40440817 G>A maps to NM_001098634.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr4:40440817 G>A maps to NM_001098634.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr4:175896930 C>T maps to NM_014269.4 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr4:175896930 C>T maps to NM_014269.4 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr5:17275408 C>T maps to NM_006317.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr5:17275408 C>T maps to NM_006317.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr5:140256418 G>A maps to NM_018903.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr5:140256418 G>A maps to NM_018903.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr7:72093937 G>A maps to NM_001145440.1 N517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr7:72093937 G>A maps to NM_001145440.1 N517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr7:103130204 G>A maps to ENST00000428762 C3249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr7:103130204 G>A maps to ENST00000428762 C3249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr8:104930678 C>T maps to NM_001100117.2 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr8:104930678 C>T maps to NM_001100117.2 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr9:125004209 T>A maps to NM_033117.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr9:125004209 T>A maps to NM_033117.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr1:5969223 A>T maps to NM_015102.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr1:5969223 A>T maps to NM_015102.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr1:36752346 T>C maps to NM_005119.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr1:36752346 T>C maps to NM_005119.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr1:157068566 G>T maps to NM_001004341.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr1:157068566 G>T maps to NM_001004341.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr10:25313144 G>A maps to NM_024838.4 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr10:25313144 G>A maps to NM_024838.4 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr11:73964551 T>C maps to NM_016147.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr11:73964551 T>C maps to NM_016147.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr14:105477588 G>A maps to NM_145701.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr14:105477588 G>A maps to NM_145701.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr15:40282487 G>A maps to NM_001013703.2 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr15:40282487 G>A maps to NM_001013703.2 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr16:66946750 G>T maps to NM_004062.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr16:66946750 G>T maps to NM_004062.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr17:43246861 C>T maps to NM_144608.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr17:43246861 C>T maps to NM_144608.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr19:18731282 G>A maps to NM_012109.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr19:18731282 G>A maps to NM_012109.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr3:183665249 C>T maps to NM_005688.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr3:183665249 C>T maps to NM_005688.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr4:158234011 C>T maps to NM_000826.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr4:158234011 C>T maps to NM_000826.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr4:186545049 G>A maps to ENST00000355634 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr4:186545049 G>A maps to ENST00000355634 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr7:70886067 C>T maps to NM_022479.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr7:70886067 C>T maps to NM_022479.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr7:86468551 C>T maps to NM_000840.2 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr7:86468551 C>T maps to NM_000840.2 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr8:104342146 G>A maps to NM_003506.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr8:104342146 G>A maps to NM_003506.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr9:117092749 C>A maps to NM_000608.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0126-01A-01D-1490-08 chr9:117092749 C>A maps to NM_000608.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr1:91405170 G>C maps to NM_201269.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr1:91405170 G>C maps to NM_201269.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr1:242048791 A>G maps to NM_006027.4 K796K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr1:242048791 A>G maps to NM_006027.4 K796K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr11:68822262 A>G maps to NM_139075.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr11:68822262 A>G maps to NM_139075.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr11:129999094 G>A maps to NM_001642.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr11:129999094 G>A maps to NM_001642.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr12:20790146 A>G maps to NM_000921.3 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr12:20790146 A>G maps to NM_000921.3 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr13:28851371 A>G did not map to a codon.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr13:28851371 A>G did not map to a codon.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr14:31081471 C>G maps to NM_017769.3 Y520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr14:31081471 C>G maps to NM_017769.3 Y520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr16:1470456 C>T maps to NM_001010878.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr16:1470456 C>T maps to NM_001010878.1 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr16:20370763 G>A maps to NM_174924.1 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr16:20370763 G>A maps to NM_174924.1 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr17:4337371 G>A maps to NM_182538.4 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr17:4337371 G>A maps to NM_182538.4 W37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr18:54694329 G>A maps to NM_015285.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr18:54694329 G>A maps to NM_015285.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr18:72345425 G>C maps to NM_017757.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr18:72345425 G>C maps to NM_017757.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr19:52394410 G>C maps to NM_023074.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr19:52394410 G>C maps to NM_023074.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr19:52394422 T>C maps to NM_023074.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr19:52394422 T>C maps to NM_023074.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr2:158626970 G>A maps to NM_001111067.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr2:158626970 G>A maps to NM_001111067.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr2:179528600 G>A maps to ENST00000392423 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr2:179528600 G>A maps to ENST00000392423 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr20:31368257 C>T maps to NM_006892.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr20:31368257 C>T maps to NM_006892.3 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr22:16287510 G>A maps to NM_001136213.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr22:16287510 G>A maps to NM_001136213.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr22:30738810 G>A maps to NM_005877.4 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr22:30738810 G>A maps to NM_005877.4 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr3:142188271 G>A maps to NM_001184.3 H2153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr3:142188271 G>A maps to NM_001184.3 H2153H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr4:2698175 T>C maps to ENST00000324666 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr4:2698175 T>C maps to ENST00000324666 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr6:109752490 G>A maps to NM_001111298.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr6:109752490 G>A maps to NM_001111298.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr7:44189582 A>G maps to NM_000162.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr7:44189582 A>G maps to NM_000162.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr7:77797371 A>T maps to NM_012301.3 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr7:77797371 A>T maps to NM_012301.3 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr9:119461598 C>T maps to NM_012210.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr9:119461598 C>T maps to NM_012210.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr11:62995958 G>A maps to NM_199352.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr11:62995958 G>A maps to NM_199352.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr12:27059332 G>T maps to NM_018164.2 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr12:27059332 G>T maps to NM_018164.2 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr12:56639371 A>C maps to NM_173595.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr12:56639371 A>C maps to NM_173595.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr12:123346051 G>A maps to NM_003959.1 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr12:123346051 G>A maps to NM_003959.1 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr19:37310869 G>A maps to NM_206894.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr19:37310869 G>A maps to NM_206894.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr20:77034 C>T maps to NM_153325.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr20:77034 C>T maps to NM_153325.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr20:2464181 A>G maps to NM_024325.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr4:2661628 C>T maps to ENST00000324666 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr4:2661628 C>T maps to ENST00000324666 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr4:56750009 C>T maps to NM_018261.3 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr4:56750009 C>T maps to NM_018261.3 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr6:123101454 G>A maps to NM_001446.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr6:123101454 G>A maps to NM_001446.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr7:95657585 C>T maps to NM_004411.4 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chr7:95657585 C>T maps to NM_004411.4 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chrX:1584563 C>T maps to NM_178129.4 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0129-01A-01D-1490-08 chrX:1584563 C>T maps to NM_178129.4 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr11:55433334 G>A maps to NM_001004704.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr11:55433334 G>A maps to NM_001004704.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr12:66725047 G>T maps to NM_033647.2 E929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr12:66725047 G>T maps to NM_033647.2 E929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr13:49039504 G>T did not map to a codon.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr13:49039504 G>T did not map to a codon.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr15:89859688 A>C maps to NM_001113378.1 *1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr15:89859688 A>C maps to NM_001113378.1 *1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr19:54875932 G>A maps to NM_002287.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr19:54875932 G>A maps to NM_002287.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr20:16496297 G>A maps to NM_024704.4 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr20:16496297 G>A maps to NM_024704.4 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr21:10951270 T>A maps to NM_199261.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr21:10951270 T>A maps to NM_199261.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr3:45077250 C>T maps to NM_003278.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr3:45077250 C>T maps to NM_003278.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr3:137991888 A>G maps to ENST00000469044 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr3:137991888 A>G maps to ENST00000469044 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr7:130139716 T>A maps to NM_002402.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr7:130139716 T>A maps to NM_002402.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr8:124518763 C>T maps to NM_058229.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr8:124518763 C>T maps to NM_058229.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr9:84607172 A>G maps to NM_001001670.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0130-01A-01D-1490-08 chr9:84607172 A>G maps to NM_001001670.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr1:7723935 C>T maps to NM_015215.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr1:7723935 C>T maps to NM_015215.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr1:7723996 C>T maps to NM_015215.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr1:7723996 C>T maps to NM_015215.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr1:145325996 A>G maps to NM_001039703.4 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr1:145325996 A>G maps to NM_001039703.4 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr12:3387672 G>A maps to ENST00000407263 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr12:3387672 G>A maps to ENST00000407263 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr19:33892681 G>A maps to NM_000285.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr19:33892681 G>A maps to NM_000285.3 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr2:73315740 C>T maps to NM_015470.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr2:73315740 C>T maps to NM_015470.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr2:149248057 C>T maps to ENST00000404807 G1619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr2:149248057 C>T maps to ENST00000404807 G1619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr2:187693301 T>C maps to NM_182521.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr2:187693301 T>C maps to NM_182521.2 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr4:167656158 A>G maps to NM_016950.2 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr4:167656158 A>G maps to NM_016950.2 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr5:132556517 G>A maps to NM_015082.1 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr5:132556517 G>A maps to NM_015082.1 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr5:140229588 G>A maps to NM_031857.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr5:140229588 G>A maps to NM_031857.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr7:107591683 G>A maps to NM_002291.2 D1126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr7:107591683 G>A maps to NM_002291.2 D1126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr8:8175744 G>A maps to NM_001080826.1 C1380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chr8:8175744 G>A maps to NM_001080826.1 C1380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chrX:36103466 G>A maps to NM_173695.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0132-01A-02D-1491-08 chrX:36103466 G>A maps to NM_173695.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:26885364 C>T maps to NM_001006665.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:26885364 C>T maps to NM_001006665.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:116666898 C>T maps to NM_152367.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:116666898 C>T maps to NM_152367.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:144873980 G>T maps to NM_014644.4 S1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:144873980 G>T maps to NM_014644.4 S1659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:149901595 T>C maps to NM_001145862.1 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:149901595 T>C maps to NM_001145862.1 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:156836716 C>T maps to NM_002529.3 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:156836716 C>T maps to NM_002529.3 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:244528020 C>T maps to NM_001012970.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr1:244528020 C>T maps to NM_001012970.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr11:7111040 T>G maps to NM_014469.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr11:7111040 T>G maps to NM_014469.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr11:35227762 C>T maps to NM_000610.3 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr11:35227762 C>T maps to NM_000610.3 R463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr12:96354262 C>T maps to NM_152435.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr12:96354262 C>T maps to NM_152435.2 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr15:33895521 C>T maps to NM_001036.3 D707D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr15:33895521 C>T maps to NM_001036.3 D707D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr16:66957763 G>A maps to NM_004165.2 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr16:66957763 G>A maps to NM_004165.2 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr16:75564090 G>A maps to NM_024533.3 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr16:75564090 G>A maps to NM_024533.3 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr17:80332604 C>T maps to NM_018949.1 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr17:80332604 C>T maps to NM_018949.1 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr18:14537856 A>G maps to ENST00000444806 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr18:14537856 A>G maps to ENST00000444806 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr18:59158010 C>T maps to NM_031891.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr18:59158010 C>T maps to NM_031891.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr18:71790684 G>A maps to NM_001142958.1 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr18:71790684 G>A maps to NM_001142958.1 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr19:5997145 G>A maps to NM_000635.3 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr19:5997145 G>A maps to NM_000635.3 D646D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr19:16259655 C>T maps to NM_032855.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr19:16259655 C>T maps to NM_032855.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr19:55143563 C>T maps to ENST00000427581 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr19:55143563 C>T maps to ENST00000427581 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr2:179497472 G>A maps to NM_133378.4 F11852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr2:179497472 G>A maps to NM_133378.4 F11852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr2:182358130 G>A maps to NM_000885.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr2:182358130 G>A maps to NM_000885.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr2:224866464 G>A maps to NM_001136530.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr2:224866464 G>A maps to NM_001136530.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr20:744503 C>T maps to NM_033409.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr20:744503 C>T maps to NM_033409.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr20:34571987 C>A maps to ENST00000373973 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr20:34571987 C>A maps to ENST00000373973 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr22:46860063 G>A maps to NM_014246.1 D1241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr22:46860063 G>A maps to NM_014246.1 D1241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:38592882 G>A maps to NM_001099404.1 I1660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:38592882 G>A maps to NM_001099404.1 I1660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:38765035 G>A maps to NM_006514.2 D1079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:38765035 G>A maps to NM_006514.2 D1079D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:38770223 G>A maps to NM_006514.2 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:38770223 G>A maps to NM_006514.2 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:121212454 G>T maps to ENST00000393672 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:121212454 G>T maps to ENST00000393672 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:187416723 G>A maps to NM_001004312.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr3:187416723 G>A maps to NM_001004312.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr5:41067250 G>A maps to ENST00000296803 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr5:41067250 G>A maps to ENST00000296803 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr6:42993025 C>A maps to NM_033112.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr6:42993025 C>A maps to NM_033112.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr7:44736642 C>T maps to ENST00000444676 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr7:44736642 C>T maps to ENST00000444676 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr7:74234527 C>T maps to NM_173537.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr7:74234527 C>T maps to NM_173537.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr8:1497704 C>T maps to ENST00000357934 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr8:1497704 C>T maps to ENST00000357934 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr8:113988210 C>T maps to NM_198123.1 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr8:113988210 C>T maps to NM_198123.1 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr9:101235478 G>A maps to NM_005458.7 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr9:101235478 G>A maps to NM_005458.7 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr9:135804223 G>T maps to NM_000368.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chr9:135804223 G>T maps to NM_000368.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:18664127 C>T maps to NM_001037343.1 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:18664127 C>T maps to NM_001037343.1 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:110925412 G>A maps to NM_001099922.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:110925412 G>A maps to NM_001099922.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:142795380 G>A maps to NM_001009615.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:142795380 G>A maps to NM_001009615.1 D99D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-0137-01A-01D-1490-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:153631648 G>A maps to ENST00000451365 S108S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-0137-01A-01D-1490-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0137-01A-01D-1490-08 chrX:153631648 G>A maps to ENST00000451365 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0139-01A-01D-1490-08 chr5:140480850 G>A maps to NM_018937.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0139-01A-01D-1490-08 chr5:140480850 G>A maps to NM_018937.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0139-01A-01D-1490-08 chr5:140960405 C>A maps to ENST00000398557 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0139-01A-01D-1490-08 chr5:140960405 C>A maps to ENST00000398557 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr10:129682095 C>T maps to NM_152311.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr10:129682095 C>T maps to NM_152311.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr13:48951143 C>T maps to NM_000321.2 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr13:48951143 C>T maps to NM_000321.2 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr15:38818584 G>A maps to NM_005739.3 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr15:38818584 G>A maps to NM_005739.3 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr16:20976073 C>T maps to NM_017539.1 T3044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr16:20976073 C>T maps to NM_017539.1 T3044T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr17:39767344 G>A maps to NM_005557.3 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr17:39767344 G>A maps to NM_005557.3 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr19:19656152 G>A maps to NM_153221.2 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr19:19656152 G>A maps to NM_153221.2 P933P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr19:49013376 C>T maps to NM_001080434.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr19:49013376 C>T maps to NM_001080434.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr2:114691914 C>T maps to NM_005721.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr2:114691914 C>T maps to NM_005721.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr2:238449109 C>A maps to NM_024101.5 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr2:238449109 C>A maps to NM_024101.5 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr3:131190113 T>C maps to ENST00000425847 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr3:131190113 T>C maps to ENST00000425847 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr4:74442416 C>T maps to NM_201431.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr4:74442416 C>T maps to NM_201431.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr4:144826670 C>T did not map to a codon.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr4:144826670 C>T did not map to a codon.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr5:153190766 G>A maps to NM_001114183.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr5:153190766 G>A maps to NM_001114183.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr6:398927 G>A maps to NM_002460.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr6:398927 G>A maps to NM_002460.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr7:1855849 C>T maps to NM_003550.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0140-01A-01D-1490-08 chr7:1855849 C>T maps to NM_003550.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr10:30739368 A>G maps to NM_005204.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr10:30739368 A>G maps to NM_005204.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr10:61831908 G>A maps to NM_020987.2 N2910N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr10:61831908 G>A maps to NM_020987.2 N2910N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr11:71277241 A>G maps to NM_001012710.1 *203W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr11:71277241 A>G maps to NM_001012710.1 *203W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr17:10430103 G>A maps to NM_017534.5 N1333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr17:10430103 G>A maps to NM_017534.5 N1333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr3:49094720 A>G maps to NM_198880.1 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr3:49094720 A>G maps to NM_198880.1 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr4:40122569 G>T maps to NM_018177.3 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr4:40122569 G>T maps to NM_018177.3 G947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr4:83372299 G>A maps to NM_021204.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr4:83372299 G>A maps to NM_021204.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr5:140263676 G>A maps to NM_018904.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr5:140263676 G>A maps to NM_018904.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr5:140604582 C>A maps to NM_018934.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0141-01A-01D-1490-08 chr5:140604582 C>A maps to NM_018934.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr1:110171968 G>A maps to ENST00000393689 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr1:110171968 G>A maps to ENST00000393689 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr1:160268960 G>A maps to NM_001098398.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr1:160268960 G>A maps to NM_001098398.1 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr15:90321327 G>A maps to NM_001039958.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr15:90321327 G>A maps to NM_001039958.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr16:81944226 C>T maps to NM_002661.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr16:81944226 C>T maps to NM_002661.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr17:7668815 C>T maps to NM_020877.2 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr17:7668815 C>T maps to NM_020877.2 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr17:10352233 G>A maps to NM_017533.2 R1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr17:10352233 G>A maps to NM_017533.2 R1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr19:17122459 G>T maps to ENST00000443236 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr19:17122459 G>T maps to ENST00000443236 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr19:36303629 G>A maps to NM_021232.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr19:36303629 G>A maps to NM_021232.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr2:219301875 C>T maps to NM_007127.2 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr2:219301875 C>T maps to NM_007127.2 N667N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr2:232457868 C>T maps to NM_152614.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr2:232457868 C>T maps to NM_152614.2 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr20:44171337 C>T did not map to a codon.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr20:44171337 C>T did not map to a codon.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr4:111397731 G>A maps to NM_001977.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr4:111397731 G>A maps to NM_001977.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr5:140605383 G>A maps to NM_018934.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr5:140605383 G>A maps to NM_018934.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr8:105361476 C>T maps to NM_030788.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr8:105361476 C>T maps to NM_030788.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr8:134144070 G>A maps to NM_003235.4 A2626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0142-01A-01D-1490-08 chr8:134144070 G>A maps to NM_003235.4 A2626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr1:183895312 A>T maps to NM_015149.3 K767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr1:183895312 A>T maps to NM_015149.3 K767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr10:55755491 G>A maps to NM_001142763.1 R934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr10:55755491 G>A maps to NM_001142763.1 R934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr10:90665246 A>T maps to NM_020799.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr10:90665246 A>T maps to NM_020799.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:8953774 G>A maps to NM_020643.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:8953774 G>A maps to NM_020643.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:49175929 G>A maps to NM_004476.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:49175929 G>A maps to NM_004476.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:60150730 C>T maps to NM_206939.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:60150730 C>T maps to NM_206939.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:89424163 C>T maps to NM_153696.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr11:89424163 C>T maps to NM_153696.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:3128314 C>T maps to NM_003213.3 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:3128314 C>T maps to NM_003213.3 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:11286158 G>A maps to NM_001097643.1 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:11286158 G>A maps to NM_001097643.1 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:52200783 C>T maps to NM_014191.2 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:52200783 C>T maps to NM_014191.2 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:113835118 G>A maps to NM_006843.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr12:113835118 G>A maps to NM_006843.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr13:25745232 G>A maps to NM_152704.2 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr13:25745232 G>A maps to NM_152704.2 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr15:50549630 G>A maps to NM_002112.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr15:50549630 G>A maps to NM_002112.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr16:15844111 C>T maps to NM_001040114.1 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr16:15844111 C>T maps to NM_001040114.1 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr17:40259775 C>T maps to NM_024119.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr17:40259775 C>T maps to NM_024119.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr17:47246246 C>T maps to NM_153446.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr17:47246246 C>T maps to NM_153446.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr17:80045207 C>T maps to NM_004104.4 K1072K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr17:80045207 C>T maps to NM_004104.4 K1072K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr19:17025571 G>A maps to ENST00000443236 F1284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr19:17025571 G>A maps to ENST00000443236 F1284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr19:55505642 G>A maps to NM_017852.3 W905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr19:55505642 G>A maps to NM_017852.3 W905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr19:56459555 C>T maps to NM_176811.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr19:56459555 C>T maps to NM_176811.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr2:109526983 G>A maps to ENST00000376651 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr2:109526983 G>A maps to ENST00000376651 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr2:120385325 C>T maps to NM_001029996.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr2:120385325 C>T maps to NM_001029996.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr2:234621855 C>T maps to NM_019078.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr2:234621855 C>T maps to NM_019078.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr20:37356996 G>A maps to NM_080552.2 W431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr20:37356996 G>A maps to NM_080552.2 W431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr21:45948428 C>T maps to ENST00000443468 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr21:45948428 C>T maps to ENST00000443468 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr4:155226288 G>A maps to NM_017639.3 T1330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr4:155226288 G>A maps to NM_017639.3 T1330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr4:185329381 A>G maps to NM_002199.3 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr4:185329381 A>G maps to NM_002199.3 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr5:1280301 C>A maps to NM_198253.2 G641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr5:1280301 C>A maps to NM_198253.2 G641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr6:146720520 C>T maps to NM_000838.3 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr6:146720520 C>T maps to NM_000838.3 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr9:4285999 G>A did not map to a codon.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chr9:4285999 G>A did not map to a codon.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:48771497 C>A maps to NM_006875.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:48771497 C>A maps to NM_006875.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:96171459 A>G maps to NM_006729.4 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:96171459 A>G maps to NM_006729.4 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:109694564 A>G maps to NM_020769.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:109694564 A>G maps to NM_020769.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:151129838 T>A did not map to a codon.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:151129838 T>A did not map to a codon.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:152801875 C>T maps to NM_001001344.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0145-01A-01W-0224-08 chrX:152801875 C>T maps to NM_001001344.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr12:52639221 C>T maps to NM_005556.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr12:52639221 C>T maps to NM_005556.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr17:38812793 G>A maps to NM_152349.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr17:38812793 G>A maps to NM_152349.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr19:57089036 C>T maps to NM_001001668.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr19:57089036 C>T maps to NM_001001668.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr21:43519222 G>A maps to NM_173568.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr21:43519222 G>A maps to NM_173568.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr9:117844147 C>T maps to NM_002160.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0151-01A-01D-1491-08 chr9:117844147 C>T maps to NM_002160.2 R769R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr1:15888816 A>C maps to NM_015291.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr1:15888816 A>C maps to NM_015291.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr1:62993825 G>C maps to ENST00000371140 S1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr1:62993825 G>C maps to ENST00000371140 S1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr1:159410402 G>A maps to NM_012351.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr1:159410402 G>A maps to NM_012351.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr10:24762770 C>T maps to NM_019590.3 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr10:24762770 C>T maps to NM_019590.3 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr12:129694196 G>A maps to NM_133448.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr12:129694196 G>A maps to NM_133448.2 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr14:38060896 G>A maps to NM_004496.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr14:38060896 G>A maps to NM_004496.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr14:94394687 C>T maps to NM_138344.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr14:94394687 C>T maps to NM_138344.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr14:94914502 C>T maps to NM_001080451.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr14:94914502 C>T maps to NM_001080451.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr17:7984476 G>A maps to NM_001139.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr17:7984476 G>A maps to NM_001139.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr17:74136122 C>A maps to NM_001454.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr17:74136122 C>A maps to NM_001454.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr18:29890191 G>A maps to ENST00000269209 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr18:29890191 G>A maps to ENST00000269209 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:10742380 G>A maps to NM_020428.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:10742380 G>A maps to NM_020428.3 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:45029206 G>A maps to NM_001102597.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:45029206 G>A maps to NM_001102597.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:53116374 T>C maps to NM_018300.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:53116374 T>C maps to NM_018300.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:56244389 G>A maps to NM_176820.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr19:56244389 G>A maps to NM_176820.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr20:8352081 C>T maps to NM_015192.2 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr20:8352081 C>T maps to NM_015192.2 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr22:20784713 A>C did not map to a codon.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr22:20784713 A>C did not map to a codon.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr3:38104256 G>A maps to NM_007335.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr3:38104256 G>A maps to NM_007335.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr5:180048196 G>A maps to NM_182925.4 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr5:180048196 G>A maps to NM_182925.4 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:38957816 G>A maps to ENST00000327475 P4349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:38957816 G>A maps to ENST00000327475 P4349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:47763199 C>T maps to ENST00000489301 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:47763199 C>T maps to ENST00000489301 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:74079389 C>T maps to NM_001080507.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:74079389 C>T maps to NM_001080507.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:76024624 G>T maps to NM_015687.2 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:76024624 G>T maps to NM_015687.2 S308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:142736936 T>C maps to NM_198569.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr6:142736936 T>C maps to NM_198569.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr7:87258210 G>C maps to NM_138290.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr7:87258210 G>C maps to NM_138290.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr7:132754902 T>C maps to ENST00000448878 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr7:132754902 T>C maps to ENST00000448878 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr8:1806267 C>A maps to ENST00000398564 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr8:1806267 C>A maps to ENST00000398564 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr8:67062092 G>T maps to NM_184085.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr8:67062092 G>T maps to NM_184085.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr9:138586906 C>T maps to NM_001101677.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0152-01A-02W-0323-08 chr9:138586906 C>T maps to NM_001101677.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr1:93301745 G>C did not map to a codon.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr1:93301745 G>C did not map to a codon.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr1:150530513 T>G maps to ENST00000369039 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr1:150530513 T>G maps to ENST00000369039 G780G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr11:56510791 C>A maps to NM_001005284.1 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr11:56510791 C>A maps to NM_001005284.1 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr11:66033174 C>T maps to NM_022822.2 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr11:66033174 C>T maps to NM_022822.2 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr11:89951305 T>C maps to NM_012124.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr11:89951305 T>C maps to NM_012124.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr12:10525754 A>G maps to NM_007360.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr12:10525754 A>G maps to NM_007360.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr15:27182398 G>A maps to NM_000810.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr15:27182398 G>A maps to NM_000810.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr15:40751043 C>T maps to NM_014952.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr15:40751043 C>T maps to NM_014952.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr17:34074266 G>A maps to NM_139285.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr17:34074266 G>A maps to NM_139285.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr19:55494685 C>T maps to NM_017852.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr19:55494685 C>T maps to NM_017852.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr20:44571847 C>T maps to NM_022104.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr20:44571847 C>T maps to NM_022104.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr21:43161993 G>A maps to ENST00000352483 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr21:43161993 G>A maps to ENST00000352483 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr3:52422624 G>A maps to ENST00000273600 K3121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr3:52422624 G>A maps to ENST00000273600 K3121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr4:46973175 C>T maps to NM_000809.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr4:46973175 C>T maps to NM_000809.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr4:69962447 C>T maps to NM_001074.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr4:69962447 C>T maps to NM_001074.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr5:140263907 C>T maps to NM_018904.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr5:140263907 C>T maps to NM_018904.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr6:138531165 G>T maps to NM_020340.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr6:138531165 G>T maps to NM_020340.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr6:161139730 G>A maps to NM_000301.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr6:161139730 G>A maps to NM_000301.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr9:91150636 C>T maps to NM_001161625.1 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr9:91150636 C>T maps to NM_001161625.1 H96H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr9:131185155 G>A maps to NM_016174.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chr9:131185155 G>A maps to NM_016174.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chrX:129200914 C>T maps to NM_001127197.1 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0154-01A-03D-1491-08 chrX:129200914 C>T maps to NM_001127197.1 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr1:16378750 C>T maps to NM_000085.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr1:16378750 C>T maps to NM_000085.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr10:11505267 G>A maps to NM_001080491.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr10:11505267 G>A maps to NM_001080491.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr12:2566753 A>G maps to NM_199460.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr12:2566753 A>G maps to NM_199460.2 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr12:72366328 T>A maps to ENST00000389376 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr12:72366328 T>A maps to ENST00000389376 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr12:130927110 G>A maps to NM_015347.4 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr12:130927110 G>A maps to NM_015347.4 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr15:42193061 G>A maps to NM_139265.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr15:42193061 G>A maps to NM_139265.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr16:553081 G>A maps to NM_014700.3 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr16:553081 G>A maps to NM_014700.3 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr18:57022800 C>A maps to NM_005570.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr18:57022800 C>A maps to NM_005570.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr19:6502175 G>T maps to NM_006087.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr19:6502175 G>T maps to NM_006087.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr19:7807927 C>T maps to NM_021155.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr19:7807927 C>T maps to NM_021155.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr19:50453361 G>T maps to NM_052884.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr19:50453361 G>T maps to NM_052884.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr21:43230602 G>A maps to NM_022115.3 H1219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr21:43230602 G>A maps to NM_022115.3 H1219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr22:37524873 C>T maps to ENST00000406505 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr22:37524873 C>T maps to ENST00000406505 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr3:93603712 G>A maps to NM_000313.3 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr3:93603712 G>A maps to NM_000313.3 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr5:64766853 C>T maps to NM_197941.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr5:64766853 C>T maps to NM_197941.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr5:71494068 A>G maps to NM_005909.3 A1629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr5:71494068 A>G maps to NM_005909.3 A1629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr5:180048668 C>T maps to NM_182925.4 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr5:180048668 C>T maps to NM_182925.4 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr6:39024211 C>T maps to NM_002062.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr6:39024211 C>T maps to NM_002062.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr6:56505354 A>G maps to ENST00000361203 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr6:56505354 A>G maps to ENST00000361203 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr6:122744039 C>A maps to NM_004506.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr6:122744039 C>A maps to NM_004506.3 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr7:104782640 G>A maps to ENST00000336613 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr7:104782640 G>A maps to ENST00000336613 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr8:145095496 G>A maps to NM_198572.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr8:145095496 G>A maps to NM_198572.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr1:173878723 G>A maps to NM_000488.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr1:173878723 G>A maps to NM_000488.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr12:11061486 G>A maps to NM_023920.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr12:11061486 G>A maps to NM_023920.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr12:122292680 G>A maps to NM_002150.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr12:122292680 G>A maps to NM_002150.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr13:110895030 C>T maps to NM_001845.4 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr13:110895030 C>T maps to NM_001845.4 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr15:99250942 G>T maps to NM_000875.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr15:99250942 G>T maps to NM_000875.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr16:89261310 C>T maps to NM_004933.2 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr16:89261310 C>T maps to NM_004933.2 Y731Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr18:7023334 G>A maps to NM_005559.2 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr18:7023334 G>A maps to NM_005559.2 G843G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr19:9063658 A>T maps to NM_024690.2 S7929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr19:9063658 A>T maps to NM_024690.2 S7929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr19:58004983 C>T maps to NM_001098491.1 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr19:58004983 C>T maps to NM_001098491.1 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr19:58018485 C>T maps to NM_198542.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr19:58018485 C>T maps to NM_198542.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr2:27803329 T>C maps to NM_032266.3 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr2:27803329 T>C maps to NM_032266.3 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr20:24565629 G>A did not map to a codon.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr20:24565629 G>A did not map to a codon.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr21:31744288 G>A maps to NM_181621.3 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr21:31744288 G>A maps to NM_181621.3 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr4:70361102 C>G maps to NM_021139.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr4:70361102 C>G maps to NM_021139.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr5:3601123 G>A maps to NM_024337.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr5:3601123 G>A maps to NM_024337.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr6:133137702 G>T did not map to a codon.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr6:133137702 G>T did not map to a codon.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr8:11607631 C>T maps to NM_002052.3 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chr8:11607631 C>T maps to NM_002052.3 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chrX:13637336 G>A maps to NM_001167890.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chrX:13637336 G>A maps to NM_001167890.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chrX:69455982 C>A maps to NM_001013579.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chrX:69455982 C>A maps to NM_001013579.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chrX:70516704 C>T maps to NM_007363.4 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0157-01A-01D-1491-08 chrX:70516704 C>T maps to NM_007363.4 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr1:154516936 C>T maps to NM_001098475.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr1:154516936 C>T maps to NM_001098475.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr1:229577743 T>C maps to NM_018230.2 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr1:229577743 T>C maps to NM_018230.2 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr11:76956337 G>A maps to ENST00000376217 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr11:76956337 G>A maps to ENST00000376217 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr11:88338070 G>A maps to NM_001143831.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr11:88338070 G>A maps to NM_001143831.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr12:68716855 C>T maps to NM_017440.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr12:68716855 C>T maps to NM_017440.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr14:36211762 T>C maps to NM_194301.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr14:36211762 T>C maps to NM_194301.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr17:7340212 T>A maps to NM_178518.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr17:7340212 T>A maps to NM_178518.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr17:78796999 G>A maps to NM_020761.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr17:78796999 G>A maps to NM_020761.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr18:67718689 C>T maps to NM_173630.3 P1760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr18:67718689 C>T maps to NM_173630.3 P1760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr19:11526628 C>T maps to NM_001161616.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr19:11526628 C>T maps to NM_001161616.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr19:40886781 C>T maps to NM_144685.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr19:40886781 C>T maps to NM_144685.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr2:54483144 C>G maps to NM_001003937.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr2:54483144 C>G maps to NM_001003937.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr21:46320233 C>T did not map to a codon.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr21:46320233 C>T did not map to a codon.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr22:29913060 C>T maps to NM_003678.4 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr22:29913060 C>T maps to NM_003678.4 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr5:837584 C>T maps to NM_024786.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr5:837584 C>T maps to NM_024786.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr5:83433170 G>A maps to NM_005711.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr5:83433170 G>A maps to NM_005711.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr6:25966963 C>T maps to NM_006355.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr6:25966963 C>T maps to NM_006355.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr6:29694675 C>T maps to NM_001098479.1 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr6:29694675 C>T maps to NM_001098479.1 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr6:49704217 A>G maps to NM_001190986.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr6:49704217 A>G maps to NM_001190986.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:53103390 C>T maps to NM_182595.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:53103390 C>T maps to NM_182595.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:82764903 C>T maps to NM_033026.5 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:82764903 C>T maps to NM_033026.5 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:98254471 C>T maps to NM_002523.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:98254471 C>T maps to NM_002523.2 N294N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-06-0158-01A-01D-1491-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-06-0158-01A-01D-1491-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:123276863 G>A maps to NM_080928.3 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0158-01A-01D-1491-08 chr7:123276863 G>A maps to NM_080928.3 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0165-01A-01D-1491-08 chr16:16101807 C>T maps to ENST00000399408 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0165-01A-01D-1491-08 chr16:16101807 C>T maps to ENST00000399408 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0165-01A-01D-1491-08 chr4:126372194 C>T maps to NM_024582.4 R3342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0165-01A-01D-1491-08 chr4:126372194 C>T maps to NM_024582.4 R3342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr1:6522119 C>A maps to ENST00000355862 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr1:6522119 C>A maps to ENST00000355862 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr10:22615861 T>G maps to NM_005180.6 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr10:22615861 T>G maps to NM_005180.6 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr12:129558862 C>A maps to NM_133448.2 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr12:129558862 C>A maps to NM_133448.2 E953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr13:101795439 G>A maps to NM_052867.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr13:101795439 G>A maps to NM_052867.2 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr15:59911700 C>T maps to NM_004751.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr15:59911700 C>T maps to NM_004751.2 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr16:16218657 G>A maps to ENST00000399408 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr16:16218657 G>A maps to ENST00000399408 V1211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr16:78064578 C>T maps to NM_005752.3 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr16:78064578 C>T maps to NM_005752.3 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr19:40328441 G>A maps to NM_001436.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr19:40328441 G>A maps to NM_001436.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr19:44981673 G>A maps to NM_013256.3 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr19:44981673 G>A maps to NM_013256.3 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr20:33851597 C>T maps to NM_006690.3 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr20:33851597 C>T maps to NM_006690.3 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr9:90537611 C>T maps to NM_001145124.1 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chr9:90537611 C>T maps to NM_001145124.1 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chrX:39932170 G>A maps to NM_001123385.1 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0166-01A-01D-1491-08 chrX:39932170 G>A maps to NM_001123385.1 R810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0167-01A-01D-1491-08 chr15:41763441 G>A maps to NM_015138.4 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0167-01A-01D-1491-08 chr15:41763441 G>A maps to NM_015138.4 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0167-01A-01D-1491-08 chr17:45905956 C>T maps to NM_145255.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0167-01A-01D-1491-08 chr17:45905956 C>T maps to NM_145255.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0167-01A-01D-1491-08 chr4:110437769 C>T maps to NM_006323.2 C700C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0167-01A-01D-1491-08 chr4:110437769 C>T maps to NM_006323.2 C700C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr1:152748960 T>C maps to ENST00000439693 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr1:152748960 T>C maps to ENST00000439693 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr1:215814044 G>A maps to ENST00000366943 D4941D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr1:215814044 G>A maps to ENST00000366943 D4941D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr1:235969723 C>T maps to NM_000081.2 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr1:235969723 C>T maps to NM_000081.2 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr10:63957963 T>C maps to NM_145307.2 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr10:63957963 T>C maps to NM_145307.2 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr11:64607006 G>A maps to NM_017525.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr11:64607006 G>A maps to NM_017525.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr13:25367335 T>C maps to ENST00000381927 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr13:25367335 T>C maps to ENST00000381927 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr13:38237608 C>T maps to NM_003306.1 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr13:38237608 C>T maps to NM_003306.1 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr15:67457244 C>T maps to NM_005902.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr15:67457244 C>T maps to NM_005902.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr17:48697120 G>A maps to NM_018896.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr17:48697120 G>A maps to NM_018896.3 L1953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr19:10254527 G>A maps to NM_001130823.1 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr19:10254527 G>A maps to NM_001130823.1 G1010G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-0168-01A-01D-1491-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr19:46997948 G>A maps to ENST00000377652 T20T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-0168-01A-01D-1491-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr19:46997948 G>A maps to ENST00000377652 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr19:47883013 C>T maps to NM_014681.5 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr19:47883013 C>T maps to NM_014681.5 S918S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr2:42883410 C>T maps to ENST00000405094 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr2:42883410 C>T maps to ENST00000405094 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr4:177190190 C>T maps to NM_080874.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr4:177190190 C>T maps to NM_080874.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr9:214613 G>T maps to NM_152569.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chr9:214613 G>T maps to NM_152569.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chrX:101972202 T>C maps to NM_138437.5 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0168-01A-01D-1491-08 chrX:101972202 T>C maps to NM_138437.5 D802D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr1:156617795 A>G maps to NM_021948.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr1:156617795 A>G maps to NM_021948.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr1:158914717 C>A maps to NM_152501.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr1:158914717 C>A maps to NM_152501.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr11:5020397 T>C maps to NM_001004755.1 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr11:5020397 T>C maps to NM_001004755.1 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr11:10580684 G>A maps to NM_006691.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr11:10580684 G>A maps to NM_006691.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr12:7069547 T>C maps to ENST00000416215 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr12:7069547 T>C maps to ENST00000416215 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr15:23006661 C>T maps to NM_030922.6 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr15:23006661 C>T maps to NM_030922.6 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr15:23811321 C>T maps to NM_005664.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr15:23811321 C>T maps to NM_005664.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr16:2147416 C>T maps to NM_001009944.2 Q3436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr16:2147416 C>T maps to NM_001009944.2 Q3436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr16:20043353 C>T maps to NM_001002911.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr16:20043353 C>T maps to NM_001002911.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr19:39591659 C>T maps to NM_001004318.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr19:39591659 C>T maps to NM_001004318.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr20:61938887 C>G maps to ENST00000326996 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr20:61938887 C>G maps to ENST00000326996 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr22:32887161 C>T maps to NM_012179.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr22:32887161 C>T maps to NM_012179.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr4:155305543 G>A maps to NM_017639.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr4:155305543 G>A maps to NM_017639.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr5:140568232 G>A maps to NM_019119.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr5:140568232 G>A maps to NM_019119.3 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr6:31322410 C>T maps to ENST00000428231 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr6:31322410 C>T maps to ENST00000428231 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr6:52370482 G>A maps to NM_012288.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr6:52370482 G>A maps to NM_012288.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr6:167790117 G>A maps to NM_004610.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr6:167790117 G>A maps to NM_004610.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr7:103270454 C>T maps to ENST00000428762 E878E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr7:103270454 C>T maps to ENST00000428762 E878E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr8:39502900 T>C maps to NM_014237.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr8:39502900 T>C maps to NM_014237.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr8:142366994 G>A maps to NM_005293.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr8:142366994 G>A maps to NM_005293.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr9:101797330 G>A maps to NM_001855.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0169-01A-01D-1490-08 chr9:101797330 G>A maps to NM_001855.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:20107155 C>T maps to NM_181719.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:20107155 C>T maps to NM_181719.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:27101097 C>T maps to NM_006015.4 G1460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:27101097 C>T maps to NM_006015.4 G1460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:156697399 G>C maps to NM_030980.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:156697399 G>C maps to NM_030980.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:247654764 C>T maps to NM_001004698.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr1:247654764 C>T maps to NM_001004698.2 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr11:122653797 G>A maps to NM_032873.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr11:122653797 G>A maps to NM_032873.4 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr13:103491944 C>T maps to NM_017693.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr13:103491944 C>T maps to NM_017693.3 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr15:74315384 C>T maps to NM_033238.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr15:74315384 C>T maps to NM_033238.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr17:4455264 C>T maps to NM_001105538.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr17:4455264 C>T maps to NM_001105538.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr17:26861356 C>T maps to NM_003593.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr17:26861356 C>T maps to NM_003593.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr17:33768201 C>T maps to NM_144682.5 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr17:33768201 C>T maps to NM_144682.5 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr18:3067532 G>A maps to NM_003803.3 N1595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr18:3067532 G>A maps to NM_003803.3 N1595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:13051172 G>T maps to NM_004343.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:13051172 G>T maps to NM_004343.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:42132050 G>A maps to NM_001817.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:42132050 G>A maps to NM_001817.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:44933284 G>A maps to NM_014518.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:44933284 G>A maps to NM_014518.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:48668865 G>A did not map to a codon.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:48668865 G>A did not map to a codon.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:54967618 C>A maps to ENST00000431846 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:54967618 C>A maps to ENST00000431846 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:56691957 C>T maps to NM_033106.3 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr19:56691957 C>T maps to NM_033106.3 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr2:26533655 G>T maps to NM_001145168.1 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr2:26533655 G>T maps to NM_001145168.1 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr2:234959450 G>A maps to NM_006944.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr2:234959450 G>A maps to NM_006944.2 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr4:165118644 T>A maps to NM_012403.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr4:165118644 T>A maps to NM_012403.1 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr6:29408232 G>A maps to NM_013941.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr6:29408232 G>A maps to NM_013941.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr6:34101000 G>A maps to NM_000841.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr6:34101000 G>A maps to NM_000841.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr6:159653415 G>A maps to NM_032532.2 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chr6:159653415 G>A maps to NM_032532.2 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chrX:47001796 T>C maps to NM_019056.5 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chrX:47001796 T>C maps to NM_019056.5 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chrX:48652345 G>A maps to NM_002049.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chrX:48652345 G>A maps to NM_002049.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chrX:67742718 G>T maps to NM_173834.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0173-01A-01D-1491-08 chrX:67742718 G>T maps to NM_173834.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr1:24710466 G>T maps to ENST00000374409 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr1:24710466 G>T maps to ENST00000374409 Y72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr1:43213878 G>A maps to NM_022356.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr1:43213878 G>A maps to NM_022356.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr1:145594169 A>T maps to NM_006468.6 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr1:145594169 A>T maps to NM_006468.6 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr10:102510547 C>T maps to NM_003987.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr10:102510547 C>T maps to NM_003987.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr12:117718571 G>A maps to ENST00000338101 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr12:126004116 C>T maps to NM_052907.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr12:126004116 C>T maps to NM_052907.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr12:129360557 C>T maps to ENST00000442111 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr12:129360557 C>T maps to ENST00000442111 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr15:42111152 C>T maps to NM_001128608.1 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr15:42111152 C>T maps to NM_001128608.1 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr16:1129416 C>T maps to NM_001053.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr16:1129416 C>T maps to NM_001053.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr17:62025417 G>A maps to NM_000334.4 F1050F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr17:62025417 G>A maps to NM_000334.4 F1050F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr19:17769034 G>T maps to ENST00000428389 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr19:17769034 G>T maps to ENST00000428389 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr19:38958337 C>T maps to NM_000540.2 F1089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr19:38958337 C>T maps to NM_000540.2 F1089F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr19:56424552 G>A maps to NM_176810.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr19:56424552 G>A maps to NM_176810.2 D210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr2:31595164 G>A maps to NM_000379.3 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr2:31595164 G>A maps to NM_000379.3 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr21:31812737 C>A maps to NM_181623.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr21:31812737 C>A maps to NM_181623.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr22:42458917 G>A maps to NM_000262.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr22:42458917 G>A maps to NM_000262.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr3:2861248 G>A maps to NM_175607.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr3:2861248 G>A maps to NM_175607.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr5:53815263 C>G maps to NM_052870.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr5:53815263 C>G maps to NM_052870.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr5:140250295 G>A maps to NM_018902.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr5:140250295 G>A maps to NM_018902.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr6:51890716 C>T maps to NM_138694.3 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr6:51890716 C>T maps to NM_138694.3 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:33397474 C>T maps to NM_198428.2 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:33397474 C>T maps to NM_198428.2 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:37989841 T>C maps to NM_017549.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:37989841 T>C maps to NM_017549.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:100197688 C>T maps to NM_012172.4 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:100197688 C>T maps to NM_012172.4 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr8:68334861 G>A maps to NM_020361.4 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr8:68334861 G>A maps to NM_020361.4 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr1:168065790 G>A maps to NM_153832.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr1:168065790 G>A maps to NM_153832.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr1:248023986 C>T maps to NM_015431.3 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr1:248023986 C>T maps to NM_015431.3 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr11:7949483 G>A maps to NM_001004461.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr11:7949483 G>A maps to NM_001004461.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr11:60150730 C>T maps to NM_206939.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr11:60150730 C>T maps to NM_206939.1 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr11:133714445 G>A maps to NM_174927.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr11:133714445 G>A maps to NM_174927.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr13:49033822 G>T did not map to a codon.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr13:49033822 G>T did not map to a codon.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr14:64496749 G>A maps to NM_182914.2 A2284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr14:64496749 G>A maps to NM_182914.2 A2284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr14:75329429 G>A maps to ENST00000445876 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr14:75329429 G>A maps to ENST00000445876 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr14:88729809 C>T maps to NM_138318.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr14:88729809 C>T maps to NM_138318.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr15:74467594 C>T maps to NM_201526.1 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr15:74467594 C>T maps to NM_201526.1 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr16:23767767 C>T maps to NM_022097.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr16:23767767 C>T maps to NM_022097.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr17:42400867 C>T maps to NM_001143780.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr17:42400867 C>T maps to NM_001143780.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr17:73827416 C>T maps to ENST00000412096 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr17:73827416 C>T maps to ENST00000412096 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr2:182360641 C>T maps to NM_000885.4 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr2:182360641 C>T maps to NM_000885.4 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr20:5903618 C>T maps to NM_001819.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr20:5903618 C>T maps to NM_001819.2 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr21:30354690 C>T did not map to a codon.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr21:30354690 C>T did not map to a codon.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr22:38274114 C>T maps to ENST00000262832 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr22:38274114 C>T maps to ENST00000262832 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr3:24231703 C>T maps to NM_001128177.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr3:24231703 C>T maps to NM_001128177.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr3:49691995 T>C maps to NM_003458.3 R1669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr3:49691995 T>C maps to NM_003458.3 R1669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr4:129770218 C>G maps to NM_199320.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr4:129770218 C>G maps to NM_199320.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr5:158140056 G>A maps to NM_024007.3 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr5:158140056 G>A maps to NM_024007.3 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr6:36993650 C>T maps to NM_173558.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr6:36993650 C>T maps to NM_173558.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr7:21698495 C>T maps to NM_003777.3 Y1730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr7:21698495 C>T maps to NM_003777.3 Y1730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr7:100364654 G>T maps to ENST00000349350 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr7:100364654 G>T maps to ENST00000349350 S1545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr9:17135248 G>A maps to NM_017738.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0184-01A-01D-1491-08 chr9:17135248 G>A maps to NM_017738.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:183511444 C>T maps to ENST00000367537 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:183511444 C>T maps to ENST00000367537 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:185972974 A>T maps to NM_031935.2 K1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:185972974 A>T maps to NM_031935.2 K1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:216373083 C>T maps to ENST00000366943 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:216373083 C>T maps to ENST00000366943 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:247654758 C>T maps to NM_001004698.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr1:247654758 C>T maps to NM_001004698.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr11:62301252 C>T maps to NM_001620.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr11:62301252 C>T maps to NM_001620.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr11:111784540 C>T maps to NM_001541.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr11:111784540 C>T maps to NM_001541.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr13:41705380 G>A maps to NM_152903.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr13:41705380 G>A maps to NM_152903.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr15:43773220 C>G did not map to a codon.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr15:43773220 C>G did not map to a codon.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr15:58006756 G>A maps to NM_001018090.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr15:58006756 G>A maps to NM_001018090.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr16:3140534 C>T maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr16:3140534 C>T maps to NM_032805.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr18:45567451 A>G maps to NM_001039360.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr18:45567451 A>G maps to NM_001039360.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr2:238283532 C>T maps to NM_004369.3 V1067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr2:238283532 C>T maps to NM_004369.3 V1067V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr20:43836502 G>T maps to NM_003007.3 G189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr20:43836502 G>T maps to NM_003007.3 G189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr20:57769722 C>T maps to NM_178457.1 R1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr20:57769722 C>T maps to NM_178457.1 R1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr3:13679196 C>A maps to NM_001165035.1 A1158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr3:13679196 C>A maps to NM_001165035.1 A1158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr4:123868605 C>T maps to NM_145207.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr4:123868605 C>T maps to NM_145207.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr4:159789509 C>T maps to ENST00000379346 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr4:159789509 C>T maps to ENST00000379346 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr5:176304268 G>A maps to NM_133369.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr5:176304268 G>A maps to NM_133369.2 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr6:168363129 G>C maps to ENST00000400822 R1620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr6:168363129 G>C maps to ENST00000400822 R1620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr7:55874787 T>A maps to NM_207366.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr7:55874787 T>A maps to NM_207366.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr7:100959699 C>T maps to NM_022777.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr7:100959699 C>T maps to NM_022777.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr8:38873653 G>A maps to NM_003816.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr8:38873653 G>A maps to NM_003816.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr9:35548293 C>A maps to NM_001135999.1 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr9:35548293 C>A maps to NM_001135999.1 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr9:37785035 G>T maps to NM_016042.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0185-01A-01W-0254-08 chr9:37785035 G>T maps to NM_016042.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr1:8390536 G>A maps to ENST00000377479 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr1:8390536 G>A maps to ENST00000377479 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr11:5013296 C>T maps to NM_021801.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr11:5013296 C>T maps to NM_021801.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr11:6007614 T>C maps to NM_001005173.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr11:6007614 T>C maps to NM_001005173.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr11:64568433 C>G maps to NM_004579.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr11:64568433 C>G maps to NM_004579.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr16:31284721 G>A maps to NM_001145808.1 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr16:31284721 G>A maps to NM_001145808.1 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr17:3850756 G>T maps to NM_174953.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr17:3850756 G>T maps to NM_174953.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr19:10434236 C>T maps to NM_133452.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr19:10434236 C>T maps to NM_133452.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr2:179498763 T>C maps to NM_133378.4 K11586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr2:179498763 T>C maps to NM_133378.4 K11586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr21:35230997 A>G maps to NM_003024.2 Q1264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr21:35230997 A>G maps to NM_003024.2 Q1264Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-0188-01A-01W-0254-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr21:43524016 C>T maps to NM_173568.3 R447*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-0188-01A-01W-0254-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr21:43524016 C>T maps to NM_173568.3 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr21:45978433 G>A maps to NM_198696.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr21:45978433 G>A maps to NM_198696.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr5:131728209 C>T maps to ENST00000435065 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr5:131728209 C>T maps to ENST00000435065 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr6:42672105 G>A maps to NM_000322.4 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr6:42672105 G>A maps to NM_000322.4 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr6:62995778 C>T maps to NM_152688.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr6:62995778 C>T maps to NM_152688.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr7:151960172 A>G maps to ENST00000355193 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr7:151960172 A>G maps to ENST00000355193 C409C. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-06-0188-01A-01W-0254-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-06-0188-01A-01W-0254-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr8:133879298 G>A maps to NM_003235.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr8:133879298 G>A maps to NM_003235.4 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr9:117129897 C>T maps to NM_030767.4 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chr9:117129897 C>T maps to NM_030767.4 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chrX:129190027 G>T maps to ENST00000303743 E1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0188-01A-01W-0254-08 chrX:129190027 G>T maps to ENST00000303743 E1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr12:53647740 G>A maps to NM_001170790.1 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr12:53647740 G>A maps to NM_001170790.1 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr17:40646355 G>A maps to NM_001130020.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr17:40646355 G>A maps to NM_001130020.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr4:70359505 G>A maps to NM_021139.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr4:70359505 G>A maps to NM_021139.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr6:45514681 G>A maps to ENST00000359524 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr6:45514681 G>A maps to ENST00000359524 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr7:73249093 C>T maps to NM_152559.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0189-01A-01D-1491-08 chr7:73249093 C>T maps to NM_152559.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:42657150 G>A maps to NM_001198850.1 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:42657150 G>A maps to NM_001198850.1 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:203316987 G>A maps to NM_002023.3 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:203316987 G>A maps to NM_002023.3 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:210008453 A>G maps to NM_014388.6 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:210008453 A>G maps to NM_014388.6 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:240071275 G>A maps to NM_000740.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:240071275 G>A maps to NM_000740.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:248637244 C>T maps to NM_001005495.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr1:248637244 C>T maps to NM_001005495.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr10:46265057 C>T maps to ENST00000399588 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr10:46265057 C>T maps to ENST00000399588 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr10:89720793 T>A maps to NM_000314.4 Y315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr10:89720793 T>A maps to NM_000314.4 Y315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr11:24936062 G>C maps to NM_001009909.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr11:24936062 G>C maps to NM_001009909.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr11:46880713 G>A maps to ENST00000256991 D1891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr11:46880713 G>A maps to ENST00000256991 D1891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr12:27521310 C>T maps to NM_020183.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr12:27521310 C>T maps to NM_020183.3 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr12:96688900 C>G did not map to a codon.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr12:96688900 C>G did not map to a codon.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr13:100634941 G>A maps to NM_007129.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr13:100634941 G>A maps to NM_007129.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr15:43038436 G>A maps to ENST00000263802 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr15:43038436 G>A maps to ENST00000263802 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr15:50838707 C>T maps to ENST00000456636 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr15:50838707 C>T maps to ENST00000456636 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr16:56973163 G>A maps to NM_014685.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr16:56973163 G>A maps to NM_014685.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr19:15770047 G>A maps to NM_000896.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr19:15770047 G>A maps to NM_000896.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr19:15989727 C>T maps to NM_001082.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr19:15989727 C>T maps to NM_001082.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr19:44223552 G>A maps to NM_019612.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr19:44223552 G>A maps to NM_019612.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr2:10560059 C>T maps to NM_002149.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr2:10560059 C>T maps to NM_002149.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr2:197183876 G>A maps to NM_020760.1 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr2:197183876 G>A maps to NM_020760.1 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr2:234869619 C>A maps to NM_024080.4 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr2:234869619 C>A maps to NM_024080.4 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr3:37369036 T>G maps to NM_001172713.1 L1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr3:37369036 T>G maps to NM_001172713.1 L1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr3:193160208 C>T maps to NM_032279.2 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr3:193160208 C>T maps to NM_032279.2 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr5:140768989 C>T maps to NM_003736.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr5:140768989 C>T maps to NM_003736.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr5:167868745 G>A maps to NM_001161661.1 W780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr5:167868745 G>A maps to NM_001161661.1 W780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr6:29455604 G>C maps to NM_052967.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr6:29455604 G>C maps to NM_052967.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr6:132966959 G>C maps to NM_138327.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr6:132966959 G>C maps to NM_138327.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr6:146350617 C>T did not map to a codon.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr6:146350617 C>T did not map to a codon.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr7:37780792 C>T maps to NM_181791.1 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr7:37780792 C>T maps to NM_181791.1 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr7:142658445 C>T did not map to a codon.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr7:142658445 C>T did not map to a codon.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr9:79322929 G>A maps to NM_015225.2 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chr9:79322929 G>A maps to NM_015225.2 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chrX:37663371 G>A maps to NM_000397.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chrX:37663371 G>A maps to NM_000397.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chrX:78426555 C>T maps to NM_032553.1 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chrX:78426555 C>T maps to NM_032553.1 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chrX:119077553 G>A maps to NM_024528.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0192-01B-01W-0348-08 chrX:119077553 G>A maps to NM_024528.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:35223554 G>A maps to NM_005268.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:35223554 G>A maps to NM_005268.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:44684376 C>T maps to NM_019100.4 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:44684376 C>T maps to NM_019100.4 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:152286041 G>A maps to NM_002016.1 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:152286041 G>A maps to NM_002016.1 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:233394107 T>C maps to NM_014801.3 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr1:233394107 T>C maps to NM_014801.3 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:7527092 G>A maps to ENST00000416109 R1128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:7527092 G>A maps to ENST00000416109 R1128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:104126948 C>T maps to NM_017564.9 R1817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:104126948 C>T maps to NM_017564.9 R1817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:113873226 G>A maps to NM_138432.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:113873226 G>A maps to NM_138432.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:125292424 G>A maps to NM_005505.4 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr12:125292424 G>A maps to NM_005505.4 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr13:48947595 C>T maps to NM_000321.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr13:48947595 C>T maps to NM_000321.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr17:47788745 C>T maps to NM_030802.3 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr17:47788745 C>T maps to NM_030802.3 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr17:73049200 G>A did not map to a codon.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr17:73049200 G>A did not map to a codon.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr19:13184251 G>A maps to ENST00000397661 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr19:13184251 G>A maps to ENST00000397661 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr2:179701793 C>T maps to NM_173648.3 R1384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr2:179701793 C>T maps to NM_173648.3 R1384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr21:47539014 C>T maps to NM_001849.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr21:47539014 C>T maps to NM_001849.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr3:32859691 G>A maps to NM_001039111.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr3:32859691 G>A maps to NM_001039111.1 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr3:149051121 C>A maps to NM_138786.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr3:149051121 C>A maps to NM_138786.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr3:193158371 G>A maps to NM_032279.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr3:193158371 G>A maps to NM_032279.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr4:2306575 G>A maps to NM_020972.2 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr4:2306575 G>A maps to NM_020972.2 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr6:152644692 G>A maps to NM_182961.2 L5279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr6:152644692 G>A maps to NM_182961.2 L5279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr7:87525786 A>T did not map to a codon.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr7:87525786 A>T did not map to a codon.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr7:149508064 G>C maps to NM_198455.2 P3156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr7:149508064 G>C maps to NM_198455.2 P3156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr9:97380088 G>A maps to NM_001127628.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chr9:97380088 G>A maps to NM_001127628.1 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chrX:39931846 G>A maps to NM_001123385.1 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chrX:39931846 G>A maps to NM_001123385.1 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chrX:50114830 C>T maps to NM_001013742.1 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0195-01B-01D-1491-08 chrX:50114830 C>T maps to NM_001013742.1 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:55136210 C>T maps to ENST00000454855 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:55136210 C>T maps to ENST00000454855 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:152084090 G>A maps to NM_007113.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:152084090 G>A maps to NM_007113.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:202287326 C>T maps to NM_001017403.1 Y632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:202287326 C>T maps to NM_001017403.1 Y632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:247921486 C>T maps to NM_012353.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr1:247921486 C>T maps to NM_012353.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr10:102749557 A>G maps to NM_021830.4 Q467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr10:102749557 A>G maps to NM_021830.4 Q467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr11:6024336 C>T maps to NM_001005179.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr11:6024336 C>T maps to NM_001005179.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr11:113677208 A>G did not map to a codon.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr11:113677208 A>G did not map to a codon.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr12:29628099 G>A maps to NM_183378.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr12:29628099 G>A maps to NM_183378.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr16:19547972 C>T maps to NM_014711.4 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr16:19547972 C>T maps to NM_014711.4 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr16:24358109 C>T maps to NM_006539.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr16:24358109 C>T maps to NM_006539.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr17:48433459 G>A maps to NM_022167.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr17:48433459 G>A maps to NM_022167.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr18:56203941 C>T maps to NM_052947.3 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr18:56203941 C>T maps to NM_052947.3 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr19:7975351 C>T maps to ENST00000425613 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr19:7975351 C>T maps to ENST00000425613 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr2:155711293 T>C maps to NM_002239.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr2:155711293 T>C maps to NM_002239.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr2:179431070 G>A maps to NM_133378.4 S24028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr2:179431070 G>A maps to NM_133378.4 S24028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr2:234669058 C>T maps to NM_000463.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr2:234669058 C>T maps to NM_000463.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:132038626 C>A maps to ENST00000403231 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:132038626 C>A maps to ENST00000403231 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:136324272 A>G maps to NM_004598.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:136324272 A>G maps to NM_004598.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:137848497 G>T maps to NM_004730.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:137848497 G>T maps to NM_004730.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:140176801 G>A maps to NM_018905.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr5:140176801 G>A maps to NM_018905.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr6:84292052 C>T maps to NM_014841.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr6:84292052 C>T maps to NM_014841.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr6:100841582 C>T maps to ENST00000262901 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chr6:100841582 C>T maps to ENST00000262901 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chrX:73963608 G>A maps to NM_001008537.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chrX:73963608 G>A maps to NM_001008537.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chrX:105152944 C>T maps to NM_198465.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0209-01A-01D-1491-08 chrX:105152944 C>T maps to NM_198465.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr1:47406940 G>A maps to ENST00000371904 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr1:47406940 G>A maps to ENST00000371904 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr1:171621316 G>T maps to NM_000261.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr1:171621316 G>T maps to NM_000261.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr10:135038288 C>G maps to ENST00000368572 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr10:135038288 C>G maps to ENST00000368572 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr11:55594993 A>G maps to NM_001004739.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr11:55594993 A>G maps to NM_001004739.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr11:92532316 A>G maps to ENST00000298047 E2046E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr11:92532316 A>G maps to ENST00000298047 E2046E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr12:7586264 C>T maps to ENST00000416109 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr12:7586264 C>T maps to ENST00000416109 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr12:52642504 C>A maps to NM_005556.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr12:52642504 C>A maps to NM_005556.3 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr12:91552213 G>A maps to NM_133503.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr12:91552213 G>A maps to NM_133503.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr13:25016085 A>G maps to NM_006437.3 F1188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr13:25016085 A>G maps to NM_006437.3 F1188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr14:105617966 G>A maps to NM_002226.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr14:105617966 G>A maps to NM_002226.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr17:62018565 C>T maps to NM_000334.4 G1692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr17:62018565 C>T maps to NM_000334.4 G1692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr19:41932545 C>T maps to NM_198540.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr19:41932545 C>T maps to NM_198540.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr2:3392023 C>T maps to NM_016030.5 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr2:3392023 C>T maps to NM_016030.5 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr2:11706612 C>T maps to NM_014668.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr2:11706612 C>T maps to NM_014668.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr2:189868847 G>A maps to NM_000090.3 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr2:189868847 G>A maps to NM_000090.3 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr6:150291167 C>T maps to NM_025218.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr6:150291167 C>T maps to NM_025218.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr6:163235288 G>A maps to NM_152410.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr6:163235288 G>A maps to NM_152410.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr7:103417021 G>A maps to ENST00000428762 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr7:103417021 G>A maps to ENST00000428762 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr9:100245440 C>G maps to NM_014290.2 S908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr9:100245440 C>G maps to NM_014290.2 S908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr9:117552980 G>A maps to NM_005118.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chr9:117552980 G>A maps to NM_005118.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chrX:119580240 G>T maps to NM_013995.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chrX:119580240 G>T maps to NM_013995.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chrX:122761606 G>A maps to NM_001081550.1 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0213-01A-01D-1491-08 chrX:122761606 G>A maps to NM_001081550.1 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr1:32843631 G>A maps to NM_001143888.1 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr1:32843631 G>A maps to NM_001143888.1 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr1:85624651 G>A maps to NM_032184.1 I1122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr1:85624651 G>A maps to NM_032184.1 I1122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr1:235940404 G>A maps to NM_000081.2 H1806H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr1:235940404 G>A maps to NM_000081.2 H1806H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr11:56950157 G>A did not map to a codon.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr11:56950157 G>A did not map to a codon.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr12:7054964 C>T maps to NM_138425.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr12:7054964 C>T maps to NM_138425.2 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr12:118298127 G>A maps to ENST00000339824 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr12:118298127 G>A maps to ENST00000339824 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr15:23811492 C>T maps to NM_005664.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr15:23811492 C>T maps to NM_005664.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr15:27193226 T>A maps to NM_000810.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr15:27193226 T>A maps to NM_000810.3 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr16:24583036 T>C maps to NM_006910.4 D1550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr16:24583036 T>C maps to NM_006910.4 D1550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr17:1456416 C>T maps to ENST00000313486 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr17:1456416 C>T maps to ENST00000313486 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr17:46937755 A>G maps to ENST00000448105 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr17:46937755 A>G maps to ENST00000448105 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr17:79220093 G>C maps to NM_001037984.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr17:79220093 G>C maps to NM_001037984.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:15132652 A>G maps to NM_173482.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:15132652 A>G maps to NM_173482.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:45494187 C>T maps to NM_001294.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:45494187 C>T maps to NM_001294.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:54968951 C>A maps to ENST00000431846 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:54968951 C>A maps to ENST00000431846 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:58319416 C>T maps to NM_024762.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr19:58319416 C>T maps to NM_024762.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr2:74900888 G>A maps to NM_004263.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr2:74900888 G>A maps to NM_004263.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr20:1615911 C>T did not map to a codon.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr20:1615911 C>T did not map to a codon.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr20:51872366 C>T maps to NM_173485.5 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr20:51872366 C>T maps to NM_173485.5 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr22:41564809 C>T maps to NM_001429.3 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr22:41564809 C>T maps to NM_001429.3 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr3:112738407 C>T maps to NM_015412.3 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr3:112738407 C>T maps to NM_015412.3 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr3:112738410 C>T maps to NM_015412.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr3:112738410 C>T maps to NM_015412.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr3:112738458 C>T maps to NM_015412.3 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr3:112738458 C>T maps to NM_015412.3 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr4:108820832 C>T maps to NM_152621.5 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr4:108820832 C>T maps to NM_152621.5 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr4:113189432 G>A maps to NM_018569.4 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr4:113189432 G>A maps to NM_018569.4 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr6:7581803 T>A did not map to a codon.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr6:7581803 T>A did not map to a codon.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr7:48312025 C>T maps to NM_152701.3 Y921Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr7:48312025 C>T maps to NM_152701.3 Y921Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr7:82581586 A>G maps to NM_033026.5 D2894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr7:82581586 A>G maps to NM_033026.5 D2894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr7:134878048 G>T maps to NM_014149.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr7:134878048 G>T maps to NM_014149.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr8:30705978 G>A maps to NM_031271.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr8:30705978 G>A maps to NM_031271.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr9:110084308 C>T maps to NM_002874.3 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr9:110084308 C>T maps to NM_002874.3 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr9:117396106 G>A maps to ENST00000374049 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0214-01A-02D-1491-08 chr9:117396106 G>A maps to ENST00000374049 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:38082339 G>A maps to NM_001038633.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:38082339 G>A maps to NM_001038633.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:114515776 G>T maps to ENST00000426820 S1163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:114515776 G>T maps to ENST00000426820 S1163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:117311263 G>A maps to NM_001767.3 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:117311263 G>A maps to NM_001767.3 Q305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:248004303 C>A maps to NM_001001959.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr1:248004303 C>A maps to NM_001001959.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr10:133787376 A>T maps to NM_004052.2 Y39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr10:133787376 A>T maps to NM_004052.2 Y39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr11:40137191 C>T maps to NM_020929.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr11:40137191 C>T maps to NM_020929.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr11:71717270 C>T maps to ENST00000393695 S1840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr11:71717270 C>T maps to ENST00000393695 S1840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr11:94040845 G>A maps to NM_001080486.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr11:94040845 G>A maps to NM_001080486.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr12:25047325 C>T maps to NM_001178093.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr12:25047325 C>T maps to NM_001178093.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr12:120142197 G>A maps to ENST00000392521 N1758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr12:120142197 G>A maps to ENST00000392521 N1758N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr12:125621256 C>T maps to NM_023928.3 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr12:125621256 C>T maps to NM_023928.3 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr16:46694425 T>G maps to NM_018206.4 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr16:46694425 T>G maps to NM_018206.4 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr16:57993925 G>A maps to NM_001297.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr16:57993925 G>A maps to NM_001297.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr17:39884046 C>T maps to ENST00000310778 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr17:39884046 C>T maps to ENST00000310778 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr19:48259847 C>T maps to NM_015710.4 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr19:48259847 C>T maps to NM_015710.4 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr2:55791467 C>T maps to NM_001122964.1 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr2:55791467 C>T maps to NM_001122964.1 K747K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr3:28381957 G>A maps to NM_022461.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr3:28381957 G>A maps to NM_022461.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr3:100951683 A>G maps to NM_016247.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr3:100951683 A>G maps to NM_016247.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr4:146077117 C>T maps to ENST00000447906 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr4:146077117 C>T maps to ENST00000447906 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr5:106762935 G>A maps to NM_001962.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr5:106762935 G>A maps to NM_001962.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr6:62604632 T>A maps to NM_152688.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr6:62604632 T>A maps to NM_152688.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr8:68419123 C>G did not map to a codon.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr8:68419123 C>G did not map to a codon.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr8:95189844 G>A maps to NM_001144663.1 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr8:95189844 G>A maps to NM_001144663.1 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr9:14307243 C>T maps to ENST00000397581 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chr9:14307243 C>T maps to ENST00000397581 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chrX:54496520 G>A maps to NM_004463.2 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chrX:54496520 G>A maps to NM_004463.2 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chrX:136113329 G>A maps to NM_054021.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0216-01B-01D-1492-08 chrX:136113329 G>A maps to NM_054021.1 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr1:248402310 T>C maps to NM_017504.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr1:248402310 T>C maps to NM_017504.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr1:249151477 G>T maps to NM_001136036.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr1:249151477 G>T maps to NM_001136036.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr10:90497504 T>C maps to NM_001080518.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr10:90497504 T>C maps to NM_001080518.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr17:33521188 A>C maps to NM_152462.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr17:33521188 A>C maps to NM_152462.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr19:45774953 G>A maps to NM_031417.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr19:45774953 G>A maps to NM_031417.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr19:52034450 G>A maps to NM_001245.5 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr19:52034450 G>A maps to NM_001245.5 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr2:20840921 C>A maps to NM_022460.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr2:20840921 C>A maps to NM_022460.3 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr3:108568056 G>T maps to NM_016388.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr3:108568056 G>T maps to NM_016388.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr3:126236442 C>T maps to NM_001165974.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr3:126236442 C>T maps to NM_001165974.1 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr3:188327128 C>T maps to NM_005578.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr3:188327128 C>T maps to NM_005578.3 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr5:101834437 T>C maps to NM_173488.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr5:101834437 T>C maps to NM_173488.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr6:97702430 A>C did not map to a codon.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr6:97702430 A>C did not map to a codon.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr7:77408001 G>A maps to NM_198467.2 W686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr7:77408001 G>A maps to NM_198467.2 W686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr8:24339683 G>A maps to ENST00000380789 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr8:24339683 G>A maps to ENST00000380789 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr8:125047529 C>T maps to NM_001039112.2 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr8:125047529 C>T maps to NM_001039112.2 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr8:144940503 G>A maps to NM_031308.1 A2306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr8:144940503 G>A maps to NM_031308.1 A2306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr9:85924521 T>C maps to NM_174938.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0219-01A-01D-1491-08 chr9:85924521 T>C maps to NM_174938.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr1:978951 C>T maps to NM_198576.2 C546C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr1:978951 C>T maps to NM_198576.2 C546C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr11:77937661 T>G maps to NM_080491.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr15:66806420 G>A maps to NM_017975.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr15:66806420 G>A maps to NM_017975.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr16:30106202 G>A maps to NM_031477.4 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr16:30106202 G>A maps to NM_031477.4 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr17:33323603 C>T maps to NM_013975.3 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr17:33323603 C>T maps to NM_013975.3 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr18:19997859 G>A did not map to a codon.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr18:19997859 G>A did not map to a codon.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr19:35850541 C>T maps to NM_005304.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr19:35850541 C>T maps to NM_005304.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr2:114257072 C>T maps to NM_012184.4 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr2:114257072 C>T maps to NM_012184.4 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr20:62122077 C>T maps to NM_001958.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr20:62122077 C>T maps to NM_001958.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr21:38380465 G>A maps to NM_018962.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr21:38380465 G>A maps to NM_018962.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr3:10084271 G>A maps to NM_033084.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr3:10084271 G>A maps to NM_033084.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr4:77252543 C>T maps to NM_001042784.1 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr4:77252543 C>T maps to NM_001042784.1 S961S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr4:177136840 A>G maps to NM_080874.3 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr4:177136840 A>G maps to NM_080874.3 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr5:55204207 C>A maps to NM_139017.4 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr5:55204207 C>A maps to NM_139017.4 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr5:118810094 G>C did not map to a codon.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr5:118810094 G>C did not map to a codon.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr5:180687304 G>A maps to NM_032765.2 H170H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr5:180687304 G>A maps to NM_032765.2 H170H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr7:151849844 T>C maps to ENST00000355193 L4214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr7:151849844 T>C maps to ENST00000355193 L4214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr8:10469369 C>T maps to NM_178857.5 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chr8:10469369 C>T maps to NM_178857.5 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chrX:48317930 G>A maps to NM_033518.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chrX:48317930 G>A maps to NM_033518.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chrX:89177185 G>A maps to NM_138960.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0237-01A-02D-1491-08 chrX:89177185 G>A maps to NM_138960.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr1:247464285 C>T maps to NM_032752.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr1:247464285 C>T maps to NM_032752.1 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr15:80883951 G>A maps to NM_014862.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr15:80883951 G>A maps to NM_014862.3 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr16:18875132 A>T maps to ENST00000389467 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr16:18875132 A>T maps to ENST00000389467 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr2:128238720 G>A maps to NM_017969.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr2:128238720 G>A maps to NM_017969.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr4:30725869 A>G maps to NM_001173523.1 K942K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr4:30725869 A>G maps to NM_001173523.1 K942K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr5:140167620 G>A maps to NM_018900.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0238-01A-02D-1492-08 chr5:140167620 G>A maps to NM_018900.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0240-01A-03D-1491-08 chr3:126133022 G>A did not map to a codon.
Sequencing variant TCGA-06-0240-01A-03D-1491-08 chr3:126133022 G>A did not map to a codon.
Sequencing variant TCGA-06-0240-01A-03D-1491-08 chr5:140167215 C>T maps to NM_018900.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0240-01A-03D-1491-08 chr5:140167215 C>T maps to NM_018900.2 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0240-01A-03D-1491-08 chr9:120466767 C>G maps to NM_138554.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0240-01A-03D-1491-08 chr9:120466767 C>G maps to NM_138554.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr1:9064867 G>A maps to NM_207420.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr1:9064867 G>A maps to NM_207420.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr1:120165749 C>A maps to NM_001080470.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr1:120165749 C>A maps to NM_001080470.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr10:29839815 G>A maps to NM_021738.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr10:29839815 G>A maps to NM_021738.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr12:57581182 C>T maps to NM_002332.2 V2325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr12:57581182 C>T maps to NM_002332.2 V2325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr15:86123971 C>T maps to NM_006738.4 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr15:86123971 C>T maps to NM_006738.4 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr16:31308884 C>T maps to NM_001145808.1 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr16:31308884 C>T maps to NM_001145808.1 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr16:67337178 C>T maps to NM_001100915.1 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr16:67337178 C>T maps to NM_001100915.1 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr19:367155 C>T maps to NM_016585.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr19:367155 C>T maps to NM_016585.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr2:101655054 G>T maps to NM_001102426.1 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr2:101655054 G>T maps to NM_001102426.1 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr3:37547524 G>A maps to NM_002207.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr3:37547524 G>A maps to NM_002207.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr5:140176219 C>T maps to NM_018905.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr5:140176219 C>T maps to NM_018905.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr5:149922521 A>G maps to NM_001543.4 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr5:149922521 A>G maps to NM_001543.4 K653K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr6:143074690 A>G maps to NM_006734.3 T2298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr6:143074690 A>G maps to NM_006734.3 T2298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr6:166571991 G>T maps to NM_003181.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr6:166571991 G>T maps to NM_003181.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr7:77973152 C>T maps to NM_012301.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr7:77973152 C>T maps to NM_012301.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr7:102953525 A>G maps to NM_014377.1 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr7:102953525 A>G maps to NM_014377.1 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr7:103281042 C>T maps to ENST00000428762 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chr7:103281042 C>T maps to ENST00000428762 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:30260975 C>T maps to NM_002367.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:30260975 C>T maps to NM_002367.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:56592045 C>T maps to NM_013444.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:56592045 C>T maps to NM_013444.3 V580V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:76937237 T>C maps to NM_000489.3 Q1170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:76937237 T>C maps to NM_000489.3 Q1170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:78427379 C>T maps to NM_032553.1 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:78427379 C>T maps to NM_032553.1 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:107412770 G>A maps to NM_033641.2 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:107412770 G>A maps to NM_033641.2 I1215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:135081057 C>T maps to NM_001042537.1 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:135081057 C>T maps to NM_001042537.1 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:153033729 C>T maps to NM_005393.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0241-01A-02D-1491-08 chrX:153033729 C>T maps to NM_005393.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr1:10192467 C>G maps to NM_001105562.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr1:10192467 C>G maps to NM_001105562.2 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr1:214815835 C>T maps to NM_016343.3 D1385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr1:214815835 C>T maps to NM_016343.3 D1385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr10:48389545 G>A maps to NM_002900.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr10:48389545 G>A maps to NM_002900.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr11:56230655 G>A maps to NM_001004743.1 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr11:56230655 G>A maps to NM_001004743.1 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr12:657399 C>T maps to NM_173593.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr12:657399 C>T maps to NM_173593.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr12:18716418 C>T maps to NM_004570.4 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr12:18716418 C>T maps to NM_004570.4 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr12:108013832 C>A maps to NM_001018072.1 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr12:108013832 C>A maps to NM_001018072.1 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr14:73578260 T>C maps to NM_021239.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr14:73578260 T>C maps to NM_021239.2 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr14:89084606 G>A maps to ENST00000380664 A1869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr14:89084606 G>A maps to ENST00000380664 A1869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr14:94847443 G>A maps to NM_001127707.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr14:94847443 G>A maps to NM_001127707.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr15:40247829 G>T maps to NM_001013703.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr15:40247829 G>T maps to NM_001013703.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr15:90784826 C>T maps to NM_001013657.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr15:90784826 C>T maps to NM_001013657.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr16:80718567 G>A maps to NM_152342.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr16:80718567 G>A maps to NM_152342.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:39408374 G>A maps to NM_017827.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:39408374 G>A maps to NM_017827.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:50397587 G>A maps to NM_172374.1 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:50397587 G>A maps to NM_172374.1 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:56953532 T>C maps to ENST00000342634 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:56953532 T>C maps to ENST00000342634 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:58131795 G>A maps to NM_003435.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr19:58131795 G>A maps to NM_003435.3 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr20:31814296 G>T did not map to a codon.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr20:31814296 G>T did not map to a codon.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr3:66449416 C>T maps to NM_015541.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr3:66449416 C>T maps to NM_015541.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr4:72338688 T>C maps to ENST00000512686 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr4:72338688 T>C maps to ENST00000512686 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr4:88362983 T>C maps to NM_024047.3 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr4:88362983 T>C maps to NM_024047.3 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr5:26906906 G>A maps to NM_016279.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr5:26906906 G>A maps to NM_016279.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr6:27219611 G>A maps to NM_005865.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr6:27219611 G>A maps to NM_005865.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr6:39162432 G>T maps to NM_003740.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr6:39162432 G>T maps to NM_003740.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr6:128319981 C>T maps to ENST00000368210 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr6:128319981 C>T maps to ENST00000368210 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr7:87083894 C>T maps to NM_018849.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr7:87083894 C>T maps to NM_018849.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr7:103137113 G>A maps to ENST00000428762 R3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr7:103137113 G>A maps to ENST00000428762 R3018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr9:33798042 C>T maps to NM_007343.3 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr9:33798042 C>T maps to NM_007343.3 C196C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr9:137622155 C>T maps to NM_000093.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chr9:137622155 C>T maps to NM_000093.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chrX:3229307 G>A maps to NM_015419.3 N2312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chrX:3229307 G>A maps to NM_015419.3 N2312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chrX:105855510 G>A maps to NM_018015.5 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0644-01A-02D-1492-08 chrX:105855510 G>A maps to NM_018015.5 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:61490355 C>T maps to NM_006133.2 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:61490355 C>T maps to NM_006133.2 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:68579933 A>G maps to NM_001876.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:68579933 A>G maps to NM_001876.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:72945704 C>T maps to NM_176071.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:72945704 C>T maps to NM_176071.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:130069960 C>T maps to NM_021978.3 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr11:130069960 C>T maps to NM_021978.3 C641C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr12:46757575 C>T maps to NM_018976.4 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr12:46757575 C>T maps to NM_018976.4 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr12:124330628 C>T maps to NM_207437.3 Y1796Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr12:124330628 C>T maps to NM_207437.3 Y1796Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr14:67864438 G>T maps to NM_016445.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr14:67864438 G>T maps to NM_016445.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr15:77473254 T>C maps to NM_024776.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr15:77473254 T>C maps to NM_024776.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr16:4834041 G>A maps to NM_144605.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr16:4834041 G>A maps to NM_144605.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr19:17086871 G>A maps to ENST00000443236 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr19:17086871 G>A maps to ENST00000443236 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr19:55107681 G>A maps to NM_006863.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr19:55107681 G>A maps to NM_006863.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr2:31483601 C>T maps to NM_014600.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr2:31483601 C>T maps to NM_014600.2 I243I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-06-0645-01A-01D-1492-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-06-0645-01A-01D-1492-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr2:163204200 T>C maps to NM_012198.3 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr2:163204200 T>C maps to NM_012198.3 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr4:8605805 G>A maps to NM_001014447.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr4:8605805 G>A maps to NM_001014447.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr5:41382220 C>T maps to NM_001005473.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr5:41382220 C>T maps to NM_001005473.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr6:152265482 C>T maps to NM_001122741.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr6:152265482 C>T maps to NM_001122741.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr7:143175835 C>T maps to NM_176883.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr7:143175835 C>T maps to NM_176883.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr8:95547142 T>C maps to NM_015496.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr8:95547142 T>C maps to NM_015496.3 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr9:105767803 G>A maps to NM_001340.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chr9:105767803 G>A maps to NM_001340.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chrX:26212571 G>A maps to NM_173523.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chrX:26212571 G>A maps to NM_173523.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chrX:119410832 G>A maps to NM_017938.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chrX:119410832 G>A maps to NM_017938.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chrX:134986678 C>T maps to NM_018666.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0645-01A-01D-1492-08 chrX:134986678 C>T maps to NM_018666.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr1:32740010 A>T maps to ENST00000373562 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr1:32740010 A>T maps to ENST00000373562 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr1:46086574 C>T maps to NM_001114938.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr1:46086574 C>T maps to NM_001114938.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr10:135203244 C>T maps to NM_152911.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr10:135203244 C>T maps to NM_152911.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr12:22778162 C>G maps to NM_018638.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr12:22778162 C>G maps to NM_018638.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr16:3458843 G>A maps to NM_003450.2 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr16:3458843 G>A maps to NM_003450.2 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr17:73555473 G>C maps to NM_001031803.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr17:73555473 G>C maps to NM_001031803.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr17:78355435 G>A maps to NM_020914.4 K4678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr17:78355435 G>A maps to NM_020914.4 K4678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr18:28584255 C>T maps to NM_001941.3 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr18:28584255 C>T maps to NM_001941.3 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr4:56348940 G>A maps to NM_004898.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr4:56348940 G>A maps to NM_004898.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr4:144141518 A>T maps to NM_032557.5 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr4:144141518 A>T maps to NM_032557.5 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr6:134493369 T>C maps to NM_001143676.1 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr6:134493369 T>C maps to NM_001143676.1 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr7:98552869 G>A maps to ENST00000359863 E1953E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr7:98552869 G>A maps to ENST00000359863 E1953E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr7:142639988 G>A maps to NM_000420.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr7:142639988 G>A maps to NM_000420.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr9:99960659 C>T maps to NM_199005.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr9:99960659 C>T maps to NM_199005.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr9:123745004 C>T maps to NM_001735.2 W1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chr9:123745004 C>T maps to NM_001735.2 W1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chrX:70823912 G>A maps to NM_052957.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chrX:70823912 G>A maps to NM_052957.4 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chrX:70823942 G>A maps to NM_052957.4 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0646-01A-01D-1492-08 chrX:70823942 G>A maps to NM_052957.4 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr1:186084451 C>T maps to NM_031935.2 L3823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr1:186084451 C>T maps to NM_031935.2 L3823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr1:214505454 C>A maps to NM_020197.2 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr1:214505454 C>A maps to NM_020197.2 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr10:18270257 G>A maps to NM_001145195.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr10:18270257 G>A maps to NM_001145195.1 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr10:128973690 C>T maps to NM_001039762.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr10:128973690 C>T maps to NM_001039762.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr12:53208028 G>A maps to NM_002272.2 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr12:53208028 G>A maps to NM_002272.2 N12N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr12:64588398 G>A maps to ENST00000311915 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr12:64588398 G>A maps to ENST00000311915 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr13:36428680 C>T maps to NM_004734.4 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr13:36428680 C>T maps to NM_004734.4 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr13:114321751 C>T maps to NM_002929.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr13:114321751 C>T maps to NM_002929.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr15:45392269 G>A maps to NM_014080.4 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr15:45392269 G>A maps to NM_014080.4 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr15:101586197 C>T maps to NM_024652.3 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr15:101586197 C>T maps to NM_024652.3 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr17:3181737 G>A maps to NM_002551.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr17:3181737 G>A maps to NM_002551.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr19:40095887 C>T maps to NM_013268.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr19:40095887 C>T maps to NM_013268.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr2:86992994 G>A maps to NM_022780.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr2:86992994 G>A maps to NM_022780.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr2:118587004 G>T maps to NM_006773.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr2:118587004 G>T maps to NM_006773.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr3:14862434 C>T maps to NM_152536.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr3:14862434 C>T maps to NM_152536.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr3:111842436 A>G maps to NM_001190259.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr3:111842436 A>G maps to NM_001190259.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:9889260 G>A maps to NM_020041.2 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:9889260 G>A maps to NM_020041.2 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:166960564 C>T maps to ENST00000507499 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:166960564 C>T maps to ENST00000507499 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:183594219 C>T maps to NM_001080477.1 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:183594219 C>T maps to NM_001080477.1 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:187557879 G>A maps to ENST00000260147 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr4:187557879 G>A maps to ENST00000260147 T1277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:94856457 G>A maps to NM_014639.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:94856457 G>A maps to NM_014639.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:148620290 C>G maps to NM_014945.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:148620290 C>G maps to NM_014945.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:171479965 C>T maps to NM_005990.3 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:171479965 C>T maps to NM_005990.3 K911K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:176765540 G>A maps to NM_006816.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr5:176765540 G>A maps to NM_006816.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr6:40359855 C>T maps to NM_020737.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr6:40359855 C>T maps to NM_020737.1 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr6:109764876 A>G maps to NM_003080.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr6:109764876 A>G maps to NM_003080.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr7:23830448 C>T maps to NM_031414.3 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr7:23830448 C>T maps to NM_031414.3 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr7:55233034 C>T maps to NM_005228.3 C595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr7:55233034 C>T maps to NM_005228.3 C595C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr9:104238681 G>A maps to NM_032342.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr9:104238681 G>A maps to NM_032342.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr9:106885400 A>G maps to NM_001042550.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0648-01A-01W-0323-08 chr9:106885400 A>G maps to NM_001042550.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:6517296 C>T maps to NM_031475.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:6517296 C>T maps to NM_031475.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:34209004 G>A maps to ENST00000373381 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:34209004 G>A maps to ENST00000373381 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:144615192 C>T maps to NM_001037675.2 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:144615192 C>T maps to NM_001037675.2 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:159802790 C>T maps to NM_020125.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:159802790 C>T maps to NM_020125.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:186088925 C>T maps to NM_031935.2 N4002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr1:186088925 C>T maps to NM_031935.2 N4002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr10:116060362 G>A maps to NM_001001936.1 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr10:116060362 G>A maps to NM_001001936.1 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr10:117607491 T>G maps to NM_207303.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr10:117607491 T>G maps to NM_207303.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr11:55703264 G>A maps to NM_006637.1 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr11:55703264 G>A maps to NM_006637.1 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr11:92624149 G>C maps to ENST00000298047 S4547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr11:92624149 G>C maps to ENST00000298047 S4547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr12:9345128 C>T maps to NM_002864.2 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr12:9345128 C>T maps to NM_002864.2 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr12:14827687 G>A maps to NM_004963.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr12:14827687 G>A maps to NM_004963.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr14:75017916 C>T maps to NM_000428.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr14:75017916 C>T maps to NM_000428.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr16:50783899 A>G maps to ENST00000311559 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr16:50783899 A>G maps to ENST00000311559 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:37687202 C>T maps to NM_016507.2 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:37687202 C>T maps to NM_016507.2 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:38812777 A>C maps to NM_152349.2 L255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:38812777 A>C maps to NM_152349.2 L255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:61657189 C>A maps to NM_005828.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:61657189 C>A maps to NM_005828.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:66033586 G>A maps to NM_002266.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:66033586 G>A maps to NM_002266.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:77081815 G>A maps to NM_001042573.1 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr17:77081815 G>A maps to NM_001042573.1 Q605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr18:28710545 C>T maps to NM_024421.2 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr18:28710545 C>T maps to NM_024421.2 E872E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:6677934 G>A maps to NM_000064.2 G1650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:6677934 G>A maps to NM_000064.2 G1650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:13876914 G>C maps to NM_001031727.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:13876914 G>C maps to NM_001031727.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:37129608 G>A maps to NM_153257.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:37129608 G>A maps to NM_153257.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:38861188 C>T maps to NM_021185.4 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:38861188 C>T maps to NM_021185.4 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:54746594 C>T maps to ENST00000407860 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:54746594 C>T maps to ENST00000407860 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr19:55449587 C>T maps to ENST00000446217 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr2:71592817 T>G maps to NM_014497.3 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr2:71592817 T>G maps to NM_014497.3 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr2:179641949 C>A maps to NM_133378.4 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr2:179641949 C>A maps to NM_133378.4 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr3:42729719 C>T maps to NM_152393.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr3:42729719 C>T maps to NM_152393.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr3:108819324 G>T maps to NM_014429.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr3:108819324 G>T maps to NM_014429.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr5:11236805 G>A maps to NM_001332.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr5:11236805 G>A maps to NM_001332.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:71130458 A>T maps to NM_022479.1 K382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:71130458 A>T maps to NM_022479.1 K382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:98254366 C>T maps to NM_002523.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:98254366 C>T maps to NM_002523.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:107720189 A>C maps to NM_007356.2 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:107720189 A>C maps to NM_007356.2 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:143095766 G>C maps to NM_005232.4 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:143095766 G>C maps to NM_005232.4 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:150269790 C>T maps to ENST00000430830 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr7:150269790 C>T maps to ENST00000430830 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr8:142367228 C>A maps to NM_005293.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr8:142367228 C>A maps to NM_005293.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr9:77377947 A>G maps to NM_017662.4 D1213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr9:77377947 A>G maps to NM_017662.4 D1213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr9:130489286 G>T maps to NM_144965.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chr9:130489286 G>T maps to NM_144965.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chrX:48775820 G>A maps to NM_006875.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chrX:48775820 G>A maps to NM_006875.3 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chrX:129155120 G>A maps to ENST00000303743 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chrX:129155120 G>A maps to ENST00000303743 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chrX:142596853 C>T maps to NM_001009609.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0649-01B-01W-0348-08 chrX:142596853 C>T maps to NM_001009609.2 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr1:1249703 G>C maps to NM_017871.4 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr1:1249703 G>C maps to NM_017871.4 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr1:151820731 G>A maps to NM_182578.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr1:151820731 G>A maps to NM_182578.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr11:48145363 G>A maps to NM_002843.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr11:48145363 G>A maps to NM_002843.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr15:54305643 C>T maps to ENST00000260323 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr15:54305643 C>T maps to ENST00000260323 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr19:4512540 C>T maps to NM_001080400.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr19:4512540 C>T maps to NM_001080400.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr3:121976020 G>A maps to NM_001178065.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr3:121976020 G>A maps to NM_001178065.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr4:70810659 C>T maps to NM_001890.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr4:70810659 C>T maps to NM_001890.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr7:120386072 G>T maps to NM_012281.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr7:120386072 G>T maps to NM_012281.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr9:8485909 C>T maps to NM_002839.3 E969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chr9:8485909 C>T maps to NM_002839.3 E969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chrX:48463239 G>A maps to NM_017883.4 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chrX:48463239 G>A maps to NM_017883.4 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chrX:48847433 G>A maps to NM_020137.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0650-01A-02D-1696-08 chrX:48847433 G>A maps to NM_020137.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr1:92946525 G>A maps to NM_005263.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr1:92946525 G>A maps to NM_005263.3 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr1:216595736 C>T did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr1:216595736 C>T did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr1:247875631 C>T maps to NM_001005286.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr1:247875631 C>T maps to NM_001005286.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr11:45946106 A>C maps to NM_152312.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr11:45946106 A>C maps to NM_152312.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr13:50589661 G>C maps to NM_173605.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr13:50589661 G>C maps to NM_173605.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr14:25043566 G>A maps to NM_001911.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr14:25043566 G>A maps to NM_001911.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr14:100118754 C>T maps to NM_001127258.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr14:100118754 C>T maps to NM_001127258.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr15:74468443 G>C maps to NM_201526.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr15:74468443 G>C maps to NM_201526.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr17:61912797 G>A maps to NM_001098426.1 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr17:61912797 G>A maps to NM_001098426.1 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr17:66928559 A>T maps to NM_007168.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr17:66928559 A>T maps to NM_007168.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr19:15758064 G>A maps to NM_000896.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr19:15758064 G>A maps to NM_000896.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr2:70680445 G>A maps to NM_003236.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr2:70680445 G>A maps to NM_003236.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr2:125660582 G>A maps to NM_130773.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr2:125660582 G>A maps to NM_130773.2 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr21:31023611 C>T did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr21:31023611 C>T did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr3:172165996 C>T maps to NM_198407.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr3:172165996 C>T maps to NM_198407.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr4:48503637 A>C did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr4:48503637 A>C did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr5:94956704 C>T maps to NM_199243.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr5:94956704 C>T maps to NM_199243.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr6:27420959 T>G maps to NM_007149.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr6:27420959 T>G maps to NM_007149.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr7:48035741 T>A maps to NM_152782.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr7:48035741 T>A maps to NM_152782.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:61769308 G>A maps to NM_017780.2 S2490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:61769308 G>A maps to NM_017780.2 S2490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:69621312 C>T maps to NM_052958.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:69621312 C>T maps to NM_052958.2 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:73849587 G>A maps to NM_004770.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:73849587 G>A maps to NM_004770.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:120569829 C>T maps to NM_006209.3 K893K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr8:120569829 C>T maps to NM_006209.3 K893K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr1:157805715 A>G maps to NM_005894.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr1:157805715 A>G maps to NM_005894.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr10:85992165 G>A maps to NM_015613.2 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr10:85992165 G>A maps to NM_015613.2 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr10:124399761 C>T maps to ENST00000368915 D2383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr10:124399761 C>T maps to ENST00000368915 D2383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:1267424 C>T maps to ENST00000447027 T3108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:1267424 C>T maps to ENST00000447027 T3108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:1267928 T>C maps to ENST00000447027 T3276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:1267928 T>C maps to ENST00000447027 T3276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:1271195 C>T maps to ENST00000447027 T4365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:1271195 C>T maps to ENST00000447027 T4365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:67765210 C>T maps to NM_030930.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr11:67765210 C>T maps to NM_030930.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr12:15654854 C>T maps to NM_030667.1 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr12:15654854 C>T maps to NM_030667.1 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr12:111748244 G>A maps to NM_015267.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr12:111748244 G>A maps to NM_015267.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr12:131487821 C>T maps to NM_198827.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr12:131487821 C>T maps to NM_198827.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr14:31425408 C>A maps to NM_001083893.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr14:31425408 C>A maps to NM_001083893.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr15:65114492 G>A maps to ENST00000333425 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr15:65114492 G>A maps to ENST00000333425 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr17:39593756 G>A maps to NM_006771.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr17:39593756 G>A maps to NM_006771.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:13008134 A>T maps to NM_000159.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:13008134 A>T maps to NM_000159.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:18327613 G>A maps to NM_000923.3 C474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:18327613 G>A maps to NM_000923.3 C474C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:19653190 C>T maps to NM_153221.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:19653190 C>T maps to NM_153221.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:22154853 A>T maps to NM_007153.3 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:22154853 A>T maps to NM_007153.3 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:36222839 C>T maps to NM_014727.1 D1823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:36222839 C>T maps to NM_014727.1 D1823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:42873136 C>T maps to ENST00000251268 T2208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:42873136 C>T maps to ENST00000251268 T2208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:53994331 G>A maps to NM_001004301.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr19:53994331 G>A maps to NM_001004301.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr2:113780341 C>T maps to NM_014438.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr2:113780341 C>T maps to NM_014438.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr20:629465 G>A maps to NM_080725.1 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr20:629465 G>A maps to NM_080725.1 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr21:39795356 G>A maps to NM_001136154.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr21:39795356 G>A maps to NM_001136154.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr21:43867264 C>T maps to NM_018961.2 N649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr21:43867264 C>T maps to NM_018961.2 N649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr22:30951881 G>A maps to NM_004861.1 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr22:30951881 G>A maps to NM_004861.1 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr3:125651538 A>C maps to NM_001195223.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:23523413 A>G maps to NM_020227.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:23523413 A>G maps to NM_020227.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:94749770 C>T maps to NM_152548.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:94749770 C>T maps to NM_152548.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:156349122 C>T maps to NM_138379.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:156349122 C>T maps to NM_138379.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr6:27293585 A>G maps to NM_032030.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr6:27293585 A>G maps to NM_032030.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr6:46806842 C>T maps to NM_005588.2 I737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr6:46806842 C>T maps to NM_005588.2 I737I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr7:98254261 G>A maps to NM_002523.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr7:98254261 G>A maps to NM_002523.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr7:112112858 C>T maps to NM_001007245.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr7:112112858 C>T maps to NM_001007245.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr8:100568722 C>T maps to NM_017890.3 I1622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr8:100568722 C>T maps to NM_017890.3 I1622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr8:113702121 C>T maps to NM_198123.1 W710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr8:113702121 C>T maps to NM_198123.1 W710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr9:114462254 G>A maps to NM_173521.3 N990N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr9:114462254 G>A maps to NM_173521.3 N990N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chrX:55650461 C>T maps to NM_198451.3 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chrX:55650461 C>T maps to NM_198451.3 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:11398781 G>A maps to NM_198516.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:11398781 G>A maps to NM_198516.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:33564671 A>G maps to ENST00000389726 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:33564671 A>G maps to ENST00000389726 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:113860379 C>T maps to NM_213621.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:113860379 C>T maps to NM_213621.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:123676406 G>A maps to NM_001005325.1 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:123676406 G>A maps to NM_001005325.1 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:123894513 C>T maps to NM_001001953.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:123894513 C>T maps to NM_001001953.1 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:123908976 A>G maps to NM_001004463.1 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr11:123908976 A>G maps to NM_001004463.1 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr14:32561266 A>G maps to NM_001030055.1 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr14:32561266 A>G maps to NM_001030055.1 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr18:7037693 C>T maps to NM_005559.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr18:7037693 C>T maps to NM_005559.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr18:43418923 C>T maps to NM_213602.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr18:43418923 C>T maps to NM_213602.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr18:61307010 C>T did not map to a codon.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr18:61307010 C>T did not map to a codon.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr19:58863691 G>A maps to NM_130786.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr19:58863691 G>A maps to NM_130786.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr2:74042972 C>T maps to NM_001080474.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr2:74042972 C>T maps to NM_001080474.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr2:234775616 G>A did not map to a codon.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr2:234775616 G>A did not map to a codon.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr22:32589174 G>A maps to NM_001098527.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr22:32589174 G>A maps to NM_001098527.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr3:87325558 G>A maps to NM_001122757.1 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr3:87325558 G>A maps to NM_001122757.1 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr3:186457115 G>A did not map to a codon.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr3:186457115 G>A did not map to a codon.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr4:175897194 C>A maps to NM_014269.4 C173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr4:175897194 C>A maps to NM_014269.4 C173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr4:186381242 G>A maps to NM_152775.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr4:186381242 G>A maps to NM_152775.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr5:33684032 G>A maps to NM_030955.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr5:33684032 G>A maps to NM_030955.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr5:79035030 G>A maps to NM_153610.3 L3481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr5:79035030 G>A maps to NM_153610.3 L3481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr6:30114886 G>A maps to ENST00000376724 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr6:30114886 G>A maps to ENST00000376724 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr7:70881028 C>T maps to NM_022479.1 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr7:70881028 C>T maps to NM_022479.1 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr7:100675947 T>C maps to NM_001040105.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr7:100675947 T>C maps to NM_001040105.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr8:97797550 T>A maps to ENST00000325141 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr8:97797550 T>A maps to ENST00000325141 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr8:105001596 C>T maps to NM_001100117.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr8:105001596 C>T maps to NM_001100117.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr8:120569919 G>A maps to NM_006209.3 D863D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr8:120569919 G>A maps to NM_006209.3 D863D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr9:90536516 A>G maps to NM_001145124.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr9:90536516 A>G maps to NM_001145124.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr9:101530446 C>T maps to ENST00000375018 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr9:101530446 C>T maps to ENST00000375018 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr9:104499634 G>A maps to NM_133445.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0744-01A-01W-0348-08 chr9:104499634 G>A maps to NM_133445.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr1:237948007 C>G maps to NM_001035.2 A4332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr1:237948007 C>G maps to NM_001035.2 A4332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr11:28058008 C>T maps to NM_031217.3 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr11:28058008 C>T maps to NM_031217.3 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr11:62298732 G>A maps to NM_001620.1 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr11:62298732 G>A maps to NM_001620.1 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr15:31294187 G>T maps to NM_002420.4 S1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr15:31294187 G>T maps to NM_002420.4 S1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr19:6714207 G>C maps to NM_000064.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr19:6714207 G>C maps to NM_000064.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr19:12187209 A>G maps to NM_001136501.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr19:12187209 A>G maps to NM_001136501.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr2:136570154 G>A maps to NM_002299.2 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr2:136570154 G>A maps to NM_002299.2 N693N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr22:24040416 G>T maps to ENST00000382833 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr22:24040416 G>T maps to ENST00000382833 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr22:29130517 C>T maps to NM_001005735.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr22:29130517 C>T maps to NM_001005735.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr3:120122087 C>T did not map to a codon.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr3:120122087 C>T did not map to a codon.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr4:70810644 T>C maps to NM_001890.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr4:70810644 T>C maps to NM_001890.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr4:83785657 G>A maps to ENST00000505472 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr4:83785657 G>A maps to ENST00000505472 Q431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr7:7412881 G>A maps to NM_001037763.2 N885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr7:7412881 G>A maps to NM_001037763.2 N885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr7:115582024 T>C maps to NM_012252.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr7:115582024 T>C maps to NM_012252.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr8:69381051 C>T maps to NM_052958.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr8:69381051 C>T maps to NM_052958.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr9:96294444 C>A maps to ENST00000333936 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chr9:96294444 C>A maps to ENST00000333936 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chrX:91090730 A>T maps to NM_032968.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0745-01A-01W-0348-08 chrX:91090730 A>T maps to NM_032968.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr1:167064115 G>A maps to NM_001080426.1 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr1:167064115 G>A maps to NM_001080426.1 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr11:65402834 G>A maps to NM_032223.2 A1700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr11:65402834 G>A maps to NM_032223.2 A1700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr12:29669419 C>A did not map to a codon.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr12:29669419 C>A did not map to a codon.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr13:61985825 G>A maps to NM_022843.3 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr13:61985825 G>A maps to NM_022843.3 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr13:113854812 G>A maps to ENST00000246505 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr13:113854812 G>A maps to ENST00000246505 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr14:105404843 C>T maps to NM_138420.2 W5648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr14:105404843 C>T maps to NM_138420.2 W5648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr15:49054659 T>G maps to NM_001194998.1 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr15:49054659 T>G maps to NM_001194998.1 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr17:73914256 G>A maps to ENST00000389570 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr17:73914256 G>A maps to ENST00000389570 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr17:74465811 C>T maps to NM_001166579.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr17:74465811 C>T maps to NM_001166579.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr18:23873444 A>G maps to ENST00000418698 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr18:23873444 A>G maps to ENST00000418698 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr19:12864092 C>T maps to NM_017682.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr19:12864092 C>T maps to NM_017682.2 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr19:49253827 G>A maps to NM_000148.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr19:49253827 G>A maps to NM_000148.3 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr20:50133366 G>A maps to NM_012340.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr20:50133366 G>A maps to NM_012340.3 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:10413513 G>A maps to NM_001001331.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:10413513 G>A maps to NM_001001331.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:49940193 A>G maps to NM_002447.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:49940193 A>G maps to NM_002447.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:52851042 C>T maps to ENST00000485816 E781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:52851042 C>T maps to ENST00000485816 E781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:98189166 A>G maps to NM_001004736.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr3:98189166 A>G maps to NM_001004736.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr4:81123200 C>T maps to NM_001099403.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr4:81123200 C>T maps to NM_001099403.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr6:27220720 C>T maps to NM_005865.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr6:27220720 C>T maps to NM_005865.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr7:112724770 C>T maps to NM_018970.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr7:112724770 C>T maps to NM_018970.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr8:56985786 A>T maps to NM_001146227.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr8:56985786 A>T maps to NM_001146227.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr8:141570506 C>T maps to NM_012154.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr8:141570506 C>T maps to NM_012154.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr9:21206994 A>G maps to NM_002171.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chr9:21206994 A>G maps to NM_002171.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chrY:5605523 C>A maps to NM_032973.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0747-01A-01W-0348-08 chrY:5605523 C>A maps to NM_032973.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr1:17990972 C>T maps to NM_018125.3 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr1:17990972 C>T maps to NM_018125.3 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr1:152276885 G>A maps to NM_002016.1 D3492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr1:152276885 G>A maps to NM_002016.1 D3492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr12:59272792 G>T maps to NM_153377.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr12:59272792 G>T maps to NM_153377.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr12:104014255 T>G maps to NM_017564.9 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr12:104014255 T>G maps to NM_017564.9 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr12:131622719 G>A maps to NM_198827.3 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr12:131622719 G>A maps to NM_198827.3 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr14:66028371 C>T maps to NM_178155.1 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr14:66028371 C>T maps to NM_178155.1 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr16:3842055 C>T maps to NM_004380.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr16:3842055 C>T maps to NM_004380.2 W419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr16:11000851 C>T maps to NM_000246.3 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr16:11000851 C>T maps to NM_000246.3 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr16:24166138 G>A maps to NM_002738.6 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr16:24166138 G>A maps to NM_002738.6 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr17:51900948 C>T maps to NM_032559.4 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr17:51900948 C>T maps to NM_032559.4 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr17:63848134 C>T maps to NM_145036.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr17:63848134 C>T maps to NM_145036.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr18:13826255 C>T maps to NM_005913.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr18:13826255 C>T maps to NM_005913.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr19:8320540 C>G maps to NM_024552.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr19:8320540 C>G maps to NM_024552.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr2:9994456 C>T maps to NM_005680.2 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr2:9994456 C>T maps to NM_005680.2 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr2:132021709 C>T maps to NM_001083538.1 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr2:132021709 C>T maps to NM_001083538.1 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr3:121980529 C>T maps to NM_001178065.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr3:121980529 C>T maps to NM_001178065.1 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr4:155413 C>T maps to NM_001039127.3 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr4:155413 C>T maps to NM_001039127.3 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr4:40440358 G>A maps to NM_001098634.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr4:40440358 G>A maps to NM_001098634.1 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr5:33596124 G>A maps to NM_030955.2 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr5:33596124 G>A maps to NM_030955.2 R856R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr5:140237258 G>A maps to NM_018901.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr5:140237258 G>A maps to NM_018901.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr6:29599227 G>A maps to NM_001470.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr6:29599227 G>A maps to NM_001470.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr7:45216986 C>T maps to NM_005856.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr7:45216986 C>T maps to NM_005856.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr7:117020041 T>C maps to NM_130768.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0749-01A-01W-0348-08 chr7:117020041 T>C maps to NM_130768.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr1:1222330 C>T maps to NM_001130413.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr1:1222330 C>T maps to NM_001130413.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr1:152281388 C>T maps to NM_002016.1 A1991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr1:152281388 C>T maps to NM_002016.1 A1991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:5068408 G>A maps to NM_001001916.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:5068408 G>A maps to NM_001001916.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:55681317 C>T maps to NM_001001960.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:55681317 C>T maps to NM_001001960.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:124294254 G>A maps to NM_001005196.1 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:124294254 G>A maps to NM_001005196.1 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:126134308 C>A maps to NM_003139.3 G551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr11:126134308 C>A maps to NM_003139.3 G551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr15:101718017 G>A maps to NM_014918.4 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr15:101718017 G>A maps to NM_014918.4 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr17:39975471 C>T maps to NM_021939.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr17:39975471 C>T maps to NM_021939.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr18:28934663 C>T maps to NM_001942.2 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr18:28934663 C>T maps to NM_001942.2 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr19:17844105 G>T maps to NM_018174.4 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr19:17844105 G>T maps to NM_018174.4 E965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr2:131521708 C>T maps to NM_001105195.1 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr2:131521708 C>T maps to NM_001105195.1 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr21:43803179 C>T maps to ENST00000380399 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr21:43803179 C>T maps to ENST00000380399 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr4:159136388 C>G maps to NM_018342.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr4:159136388 C>G maps to NM_018342.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr6:86253475 C>A maps to NM_153816.3 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0750-01A-01W-0348-08 chr6:86253475 C>A maps to NM_153816.3 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr1:152282712 G>C maps to NM_002016.1 S1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr1:152282712 G>C maps to NM_002016.1 S1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr12:4643362 A>C maps to NM_020374.2 L95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr12:4643362 A>C maps to NM_020374.2 L95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr12:7295763 C>T maps to NM_014718.3 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr12:7295763 C>T maps to NM_014718.3 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr12:124416576 G>A maps to NM_207437.3 R4288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr12:124416576 G>A maps to NM_207437.3 R4288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr14:47351247 A>G maps to NM_001113498.2 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr14:47351247 A>G maps to NM_001113498.2 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr14:96949426 C>T maps to NM_152327.2 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr14:96949426 C>T maps to NM_152327.2 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr16:70551627 C>G maps to NM_015386.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr16:70551627 C>G maps to NM_015386.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr16:84812552 C>A maps to NM_005153.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr16:84812552 C>A maps to NM_005153.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr17:5991316 C>T maps to NM_015253.1 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr17:5991316 C>T maps to NM_015253.1 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr17:26816245 G>A maps to NM_001145975.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr17:26816245 G>A maps to NM_001145975.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr19:57722986 G>A maps to NM_003417.4 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr19:57722986 G>A maps to NM_003417.4 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr20:5904211 C>T maps to NM_001819.2 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr20:5904211 C>T maps to NM_001819.2 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr21:45825916 G>A maps to ENST00000397932 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr21:45825916 G>A maps to ENST00000397932 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr5:13735336 G>A maps to NM_001369.2 Y3888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr5:13735336 G>A maps to NM_001369.2 Y3888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr5:140256979 C>T maps to NM_018903.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr5:140256979 C>T maps to NM_018903.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr6:84233952 C>T maps to NM_153362.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr6:84233952 C>T maps to NM_153362.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr7:87035602 C>T did not map to a codon.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr7:87035602 C>T did not map to a codon.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr7:93518518 G>A maps to NM_006528.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr7:93518518 G>A maps to NM_006528.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr7:100816792 C>T maps to NM_198571.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chr7:100816792 C>T maps to NM_198571.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chrX:31089887 G>A maps to NM_031894.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0875-01A-01W-0424-08 chrX:31089887 G>A maps to NM_031894.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr1:34070880 C>T did not map to a codon.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr1:34070880 C>T did not map to a codon.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr1:210637954 C>T maps to NM_001170580.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr1:210637954 C>T maps to NM_001170580.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr11:48266855 C>T maps to NM_001004727.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr11:48266855 C>T maps to NM_001004727.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr12:68551724 G>A maps to NM_000619.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr12:68551724 G>A maps to NM_000619.2 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr13:33017655 G>A maps to NM_033111.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr13:33017655 G>A maps to NM_033111.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr15:91454399 G>A did not map to a codon.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr15:91454399 G>A did not map to a codon.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr16:5135683 C>T maps to NM_201400.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr16:5135683 C>T maps to NM_201400.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr17:6338337 G>A maps to NM_014336.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr17:6338337 G>A maps to NM_014336.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr17:21319709 C>T maps to NM_021012.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr17:21319709 C>T maps to NM_021012.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:8661030 A>G maps to NM_030957.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:8661030 A>G maps to NM_030957.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:22155609 A>G maps to NM_007153.3 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:22155609 A>G maps to NM_007153.3 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:51629377 C>T maps to NM_014441.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:51629377 C>T maps to NM_014441.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:51728756 C>T maps to NM_001772.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr19:51728756 C>T maps to NM_001772.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr2:128631553 C>A maps to NM_031445.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr2:128631553 C>A maps to NM_031445.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr21:46032418 C>T maps to NM_198695.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr21:46032418 C>T maps to NM_198695.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr4:79385646 C>T maps to NM_025074.6 P2313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr4:79385646 C>T maps to NM_025074.6 P2313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr5:143327 C>T maps to NM_052909.3 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr5:143327 C>T maps to NM_052909.3 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr5:159344025 C>T maps to NM_000679.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr5:159344025 C>T maps to NM_000679.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:22165267 G>A maps to ENST00000344041 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:22165267 G>A maps to ENST00000344041 I679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:111395649 C>T maps to ENST00000428084 W1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:111395649 C>T maps to ENST00000428084 W1446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:116960623 G>A maps to NM_003391.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:116960623 G>A maps to NM_003391.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:129813713 G>A maps to NM_032842.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr7:129813713 G>A maps to NM_032842.3 D470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr8:24254920 C>T maps to NM_014479.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr8:24254920 C>T maps to NM_014479.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr8:59492352 G>A maps to NM_005625.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr8:59492352 G>A maps to NM_005625.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr9:439372 G>A maps to NM_203447.3 A1736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr9:439372 G>A maps to NM_203447.3 A1736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr9:117020835 C>T maps to NM_032888.2 R1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chr9:117020835 C>T maps to NM_032888.2 R1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:3021959 G>A maps to NM_004042.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:3021959 G>A maps to NM_004042.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:39930271 C>T maps to NM_001123385.1 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:39930271 C>T maps to NM_001123385.1 S1064S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:53573430 G>A maps to ENST00000276009 A3629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:53573430 G>A maps to ENST00000276009 A3629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:105153108 G>A maps to NM_198465.2 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:105153108 G>A maps to NM_198465.2 Q492Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:118893487 G>A maps to NM_001105576.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0876-01A-01W-0424-08 chrX:118893487 G>A maps to NM_001105576.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr1:170961346 C>T maps to NM_001163629.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr1:170961346 C>T maps to NM_001163629.1 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr1:237604755 C>T maps to NM_001035.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr1:237604755 C>T maps to NM_001035.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr10:72517794 C>T maps to NM_139155.2 C1008C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr10:72517794 C>T maps to NM_139155.2 C1008C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr10:120801815 C>G maps to NM_003750.2 G1072G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr10:120801815 C>G maps to NM_003750.2 G1072G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr11:56468274 A>T maps to NM_001013358.1 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr11:56468274 A>T maps to NM_001013358.1 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr11:113815367 C>G maps to NM_006028.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr11:113815367 C>G maps to NM_006028.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr12:111748124 C>T maps to NM_015267.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr12:111748124 C>T maps to NM_015267.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr13:75933903 C>T did not map to a codon.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr13:75933903 C>T did not map to a codon.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr15:74425373 C>T maps to NM_001130137.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr15:74425373 C>T maps to NM_001130137.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr16:56928512 C>T maps to NM_000339.2 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr16:56928512 C>T maps to NM_000339.2 F873F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr17:16321182 G>A did not map to a codon.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr17:16321182 G>A did not map to a codon.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr17:41003668 G>A maps to NM_003734.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr17:41003668 G>A maps to NM_003734.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr18:33257554 G>A maps to NM_020474.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr18:33257554 G>A maps to NM_020474.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr18:77918373 C>T maps to NM_032510.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr18:77918373 C>T maps to NM_032510.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:6680226 G>T maps to NM_000064.2 Y1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:6680226 G>T maps to NM_000064.2 Y1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:38633314 G>T maps to NM_015073.1 S1166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:38633314 G>T maps to NM_015073.1 S1166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:40097888 C>T maps to NM_013268.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:40097888 C>T maps to NM_013268.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:52942495 C>T maps to NM_001143939.1 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:52942495 C>T maps to NM_001143939.1 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:56701663 C>T maps to NM_001080456.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr19:56701663 C>T maps to NM_001080456.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr2:29386733 C>G maps to ENST00000379543 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr2:29386733 C>G maps to ENST00000379543 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr22:19318995 A>G maps to NM_003325.3 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr22:19318995 A>G maps to NM_003325.3 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr3:27761788 G>A maps to ENST00000449599 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr3:27761788 G>A maps to ENST00000449599 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr3:52840312 C>T maps to NM_002217.3 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr3:52840312 C>T maps to NM_002217.3 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr3:129694826 G>A maps to NM_007117.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr3:129694826 G>A maps to NM_007117.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr4:69696458 C>G maps to NM_001075.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr4:69696458 C>G maps to NM_001075.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr6:49574863 T>G maps to NM_000324.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr6:49574863 T>G maps to NM_000324.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr7:107350616 A>G maps to NM_000441.1 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr7:107350616 A>G maps to NM_000441.1 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr8:28017798 G>A maps to NM_018091.5 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr8:28017798 G>A maps to NM_018091.5 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr8:70744581 G>A maps to NM_030958.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr8:70744581 G>A maps to NM_030958.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr9:19786745 A>C maps to NM_020344.2 L40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr9:19786745 A>C maps to NM_020344.2 L40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr9:35609459 G>A maps to NM_006285.2 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chr9:35609459 G>A maps to NM_006285.2 W534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chrX:69479144 G>A maps to NM_002565.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0877-01A-01W-0424-08 chrX:69479144 G>A maps to NM_002565.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr1:157667596 T>C maps to NM_052939.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr1:157667596 T>C maps to NM_052939.3 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr11:55873033 C>T maps to NM_001005200.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr11:55873033 C>T maps to NM_001005200.1 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:54913071 C>T maps to NM_005337.4 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:54913071 C>T maps to NM_005337.4 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:81688793 C>T maps to NM_003625.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:81688793 C>T maps to NM_003625.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:109843785 C>T maps to NM_001101421.3 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:109843785 C>T maps to NM_001101421.3 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:112703782 C>T maps to NM_001109662.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr12:112703782 C>T maps to NM_001109662.2 E617E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr16:84472801 G>A maps to ENST00000416219 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr16:84472801 G>A maps to ENST00000416219 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr2:196865487 G>A maps to NM_018897.2 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr2:196865487 G>A maps to NM_018897.2 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr21:32007725 T>A maps to NM_181616.1 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr21:32007725 T>A maps to NM_181616.1 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr4:1206063 G>C maps to NM_001328.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr4:1206063 G>C maps to NM_001328.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr5:140222516 G>A maps to NM_018911.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr5:140222516 G>A maps to NM_018911.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr6:55142305 A>G maps to NM_001526.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr6:55142305 A>G maps to NM_001526.3 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:31016924 C>T maps to NM_000823.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:31016924 C>T maps to NM_000823.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:55221780 C>T maps to NM_005228.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:55221780 C>T maps to NM_005228.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:55221795 C>T maps to NM_005228.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:55221795 C>T maps to NM_005228.3 N280N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:100350610 A>G maps to ENST00000349350 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:100350610 A>G maps to ENST00000349350 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:151892992 T>C maps to ENST00000355193 S1459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr7:151892992 T>C maps to ENST00000355193 S1459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr9:113704319 A>C maps to NM_057159.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr9:113704319 A>C maps to NM_057159.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr9:123675734 C>T maps to NM_001190945.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0878-01A-01W-0424-08 chr9:123675734 C>T maps to NM_001190945.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:28285084 G>A maps to NM_014474.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:28285084 G>A maps to NM_014474.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:103345385 A>G maps to NM_080629.2 N1721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:103345385 A>G maps to NM_080629.2 N1721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:110740738 A>G maps to NM_001010898.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:110740738 A>G maps to NM_001010898.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:183542319 C>T maps to NM_001127651.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr1:183542319 C>T maps to NM_001127651.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr10:5541185 C>T maps to NM_017422.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr10:5541185 C>T maps to NM_017422.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr10:106899183 C>T maps to NM_014978.1 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr10:106899183 C>T maps to NM_014978.1 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr12:97087576 A>G maps to ENST00000342887 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr12:97087576 A>G maps to ENST00000342887 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr12:130926696 C>T maps to NM_015347.4 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr12:130926696 C>T maps to NM_015347.4 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr13:32910999 T>C maps to NM_000059.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr13:32910999 T>C maps to NM_000059.3 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr13:50204951 G>A maps to NM_138450.5 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr13:50204951 G>A maps to NM_138450.5 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr14:94703971 C>T maps to NM_058237.1 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr14:94703971 C>T maps to NM_058237.1 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr19:41597725 C>T maps to NM_000766.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr19:41597725 C>T maps to NM_000766.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr19:55624064 C>T maps to NM_017607.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr19:55624064 C>T maps to NM_017607.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr2:70524588 G>A maps to ENST00000430566 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr2:70524588 G>A maps to ENST00000430566 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr2:166847870 T>A maps to NM_001165963.1 K1972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr2:166847870 T>A maps to NM_001165963.1 K1972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr2:233405385 C>T maps to NM_005199.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr2:233405385 C>T maps to NM_005199.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr20:47309261 C>T maps to NM_020820.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr20:47309261 C>T maps to NM_020820.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr22:46708129 G>A maps to NM_016426.6 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr22:46708129 G>A maps to NM_016426.6 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr3:9034618 C>T maps to NM_014850.2 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr3:9034618 C>T maps to NM_014850.2 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr5:140481942 G>A maps to NM_018937.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr5:140481942 G>A maps to NM_018937.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr5:140782947 C>T maps to NM_018921.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr5:140782947 C>T maps to NM_018921.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr6:90387329 G>A maps to NM_014611.1 S4166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr6:90387329 G>A maps to NM_014611.1 S4166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr8:25225731 C>T maps to NM_024940.6 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0879-01A-01W-0424-08 chr8:25225731 C>T maps to NM_024940.6 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr16:61687973 C>T maps to NM_001796.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr16:61687973 C>T maps to NM_001796.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr19:56459234 G>A did not map to a codon.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr19:56459234 G>A did not map to a codon.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr2:167141061 G>A maps to ENST00000303354 N626N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr2:167141061 G>A maps to ENST00000303354 N626N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr2:179615120 A>G maps to ENST00000375038 T4004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr2:179615120 A>G maps to ENST00000375038 T4004T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr4:73962982 T>G maps to NM_032217.3 S1676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr4:73962982 T>G maps to NM_032217.3 S1676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr5:140563144 G>T maps to NM_020957.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr5:140563144 G>T maps to NM_020957.1 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr5:140720391 G>A maps to NM_018915.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr5:140720391 G>A maps to NM_018915.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr6:30690336 A>G maps to NM_178014.2 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr6:30690336 A>G maps to NM_178014.2 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr8:95188832 G>A maps to NM_001144663.1 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr8:95188832 G>A maps to NM_001144663.1 N120N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr9:90536516 A>T maps to NM_001145124.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0881-01A-02W-0424-08 chr9:90536516 A>T maps to NM_001145124.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr1:176661412 T>C maps to NM_020318.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr1:176661412 T>C maps to NM_020318.2 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr13:40175281 G>A maps to NM_005780.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr13:40175281 G>A maps to NM_005780.2 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr15:41810013 T>C maps to NM_015540.2 T1338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr15:41810013 T>C maps to NM_015540.2 T1338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr16:16225755 C>T maps to ENST00000399408 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr16:16225755 C>T maps to ENST00000399408 L1320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr16:67683168 C>T maps to NM_001013838.1 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr16:67683168 C>T maps to NM_001013838.1 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:18708851 A>G did not map to a codon.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:18708851 A>G did not map to a codon.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:34261841 G>T maps to NM_020426.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:34261841 G>T maps to NM_020426.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:46703537 G>A maps to NM_024017.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:46703537 G>A maps to NM_024017.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:65041000 C>T maps to NM_000727.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr17:65041000 C>T maps to NM_000727.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr18:6978309 C>T maps to NM_005559.2 T2025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr18:6978309 C>T maps to NM_005559.2 T2025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr19:24309635 C>T maps to NM_203282.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr19:24309635 C>T maps to NM_203282.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr19:57669794 T>C maps to NM_001012729.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr19:57669794 T>C maps to NM_001012729.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr3:46414782 C>T maps to NM_001100168.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr3:46414782 C>T maps to NM_001100168.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr3:52543898 C>T maps to NM_015136.2 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr3:52543898 C>T maps to NM_015136.2 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr4:55984939 C>T maps to NM_002253.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr4:55984939 C>T maps to NM_002253.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr6:50810942 C>A maps to ENST00000263046 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr6:50810942 C>A maps to ENST00000263046 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr7:126086219 G>A maps to NM_001127323.1 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr7:126086219 G>A maps to NM_001127323.1 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr8:37732070 G>A maps to NM_001002814.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0882-01A-01W-0424-08 chr8:37732070 G>A maps to NM_001002814.2 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr1:154918741 T>G maps to NM_020524.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr1:154918741 T>G maps to NM_020524.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr1:206942019 G>A maps to NM_000572.2 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr1:206942019 G>A maps to NM_000572.2 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr10:50532017 C>T maps to NM_001135196.1 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr10:50532017 C>T maps to NM_001135196.1 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr11:56344525 C>T maps to NM_001004741.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr11:56344525 C>T maps to NM_001004741.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr11:96074999 C>G maps to NM_032427.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr11:96074999 C>G maps to NM_032427.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr11:107501262 G>A maps to NM_018712.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr11:107501262 G>A maps to NM_018712.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr12:117977617 C>T maps to ENST00000339824 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr12:117977617 C>T maps to ENST00000339824 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr14:23820968 G>A maps to NM_020372.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr14:23820968 G>A maps to NM_020372.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr14:44975095 A>G maps to NM_032135.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr14:44975095 A>G maps to NM_032135.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr15:43748819 C>T maps to NM_001141980.1 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr15:43748819 C>T maps to NM_001141980.1 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:3486724 C>G did not map to a codon.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:3486724 C>G did not map to a codon.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:37295948 G>T maps to NM_020405.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:37295948 G>T maps to NM_020405.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:39661433 G>A maps to NM_153490.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:39661433 G>A maps to NM_153490.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:60679466 G>A maps to ENST00000326270 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr17:60679466 G>A maps to ENST00000326270 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr19:40580617 T>C maps to NM_001142577.1 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr19:40580617 T>C maps to NM_001142577.1 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr20:50407986 C>T maps to NM_020436.3 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr20:50407986 C>T maps to NM_020436.3 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr22:17072540 G>A maps to NM_014406.4 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr22:17072540 G>A maps to NM_014406.4 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr22:44586518 C>T maps to NM_001137606.1 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr22:44586518 C>T maps to NM_001137606.1 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr4:266351 A>G maps to ENST00000419098 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr4:266351 A>G maps to ENST00000419098 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr4:39267693 C>T maps to NM_025132.3 A1065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr4:39267693 C>T maps to NM_025132.3 A1065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr4:156721200 G>T maps to ENST00000502959 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr4:156721200 G>T maps to ENST00000502959 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr5:75428009 C>T maps to NM_014979.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr5:75428009 C>T maps to NM_014979.1 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr5:178581108 G>A maps to NM_014244.4 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr5:178581108 G>A maps to NM_014244.4 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr6:100896121 C>T maps to ENST00000262901 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr6:100896121 C>T maps to ENST00000262901 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr6:107008786 C>T maps to NM_001624.2 R1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr6:107008786 C>T maps to NM_001624.2 R1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr6:139488186 G>A maps to NM_016217.2 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr6:139488186 G>A maps to NM_016217.2 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:36768587 C>T maps to NM_001031836.2 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:36768587 C>T maps to NM_001031836.2 I824I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:70744272 G>A maps to NM_030958.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:70744272 G>A maps to NM_030958.2 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:131414153 C>A maps to NM_018482.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:131414153 C>A maps to NM_018482.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:142231733 G>A maps to NM_001080431.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr8:142231733 G>A maps to NM_001080431.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr9:107298584 C>T maps to NM_001001961.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chr9:107298584 C>T maps to NM_001001961.1 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:37665737 C>T maps to NM_000397.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:37665737 C>T maps to NM_000397.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:49455936 T>C maps to NM_003785.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:49455936 T>C maps to NM_003785.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:119005258 C>T maps to NM_006978.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:119005258 C>T maps to NM_006978.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:144904764 G>A maps to NM_001144010.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:144904764 G>A maps to NM_001144010.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:153229663 G>T maps to ENST00000369984 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0939-01A-01D-1353-08 chrX:153229663 G>T maps to ENST00000369984 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:17316633 C>T maps to NM_022089.2 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:17316633 C>T maps to NM_022089.2 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:19166668 G>A maps to NM_152232.2 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:19166668 G>A maps to NM_152232.2 I648I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:21009289 G>A maps to NM_020816.2 Y773Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:21009289 G>A maps to NM_020816.2 Y773Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:152275640 G>A maps to NM_002016.1 R3907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:152275640 G>A maps to NM_002016.1 R3907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:155161952 T>C maps to ENST00000425082 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:155161952 T>C maps to ENST00000425082 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:156503842 G>A maps to NM_178229.4 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr1:156503842 G>A maps to NM_178229.4 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr10:26305806 G>A maps to NM_017433.4 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr10:26305806 G>A maps to NM_017433.4 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr11:60470942 C>T maps to NM_031457.1 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr11:60470942 C>T maps to NM_031457.1 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr11:60739381 C>A maps to NM_006725.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr11:60739381 C>A maps to NM_006725.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr14:21876715 T>C did not map to a codon.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr14:21876715 T>C did not map to a codon.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr16:10274211 G>A maps to NM_000833.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr16:10274211 G>A maps to NM_000833.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr16:23505699 C>T did not map to a codon.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr16:23505699 C>T did not map to a codon.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr16:57017289 C>T maps to NM_000078.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr16:57017289 C>T maps to NM_000078.2 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:8784087 C>T maps to NM_001142633.1 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:8784087 C>T maps to NM_001142633.1 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:21318734 C>T maps to NM_021012.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:21318734 C>T maps to NM_021012.4 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:62144065 C>T maps to NM_001433.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:62144065 C>T maps to NM_001433.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:77081746 C>T maps to NM_001042573.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr17:77081746 C>T maps to NM_001042573.1 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr19:49686169 C>T maps to NM_017636.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr19:49686169 C>T maps to NM_017636.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr2:238275696 G>C maps to NM_004369.3 Y1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr2:238275696 G>C maps to NM_004369.3 Y1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr20:46318883 G>A maps to NM_001161841.1 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr20:46318883 G>A maps to NM_001161841.1 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr21:47535811 G>A maps to NM_001849.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr21:47535811 G>A maps to NM_001849.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr3:10387070 C>T maps to NM_001001331.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr3:10387070 C>T maps to NM_001001331.2 T900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr3:128696987 T>C maps to NM_020741.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr3:128696987 T>C maps to NM_020741.2 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr3:137717742 C>T maps to NM_001002026.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr3:137717742 C>T maps to NM_001002026.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr4:123374885 G>A maps to NM_000586.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr4:123374885 G>A maps to NM_000586.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr4:155719189 C>T maps to NM_144979.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr4:155719189 C>T maps to NM_144979.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr4:156632018 G>A maps to NM_001130684.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr4:156632018 G>A maps to NM_001130684.1 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr5:140256670 C>T maps to NM_018903.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr5:140256670 C>T maps to NM_018903.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr5:146030194 A>T maps to ENST00000394414 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr5:146030194 A>T maps to ENST00000394414 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr8:24200681 C>A maps to NM_014265.4 C633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr8:24200681 C>A maps to NM_014265.4 C633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr8:25203033 C>T maps to NM_024940.6 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr8:25203033 C>T maps to NM_024940.6 S887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr8:110588240 C>A maps to NM_001099744.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr8:110588240 C>A maps to NM_001099744.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr9:140904510 C>T maps to ENST00000277549 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chr9:140904510 C>T maps to ENST00000277549 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:8138150 C>T maps to NM_016378.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:8138150 C>T maps to NM_016378.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:22112132 T>C maps to NM_000444.4 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:22112132 T>C maps to NM_000444.4 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:53600811 A>G maps to ENST00000276009 T2070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:53600811 A>G maps to ENST00000276009 T2070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:115303790 C>T maps to NM_000686.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1804-01A-01D-1696-08 chrX:115303790 C>T maps to NM_000686.4 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr1:248224276 T>A maps to NM_001004687.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr1:248224276 T>A maps to NM_001004687.1 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr12:41967364 C>T maps to NM_001164595.1 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr12:41967364 C>T maps to NM_001164595.1 D928D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr15:86286790 G>A maps to NM_006738.4 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr15:86286790 G>A maps to NM_006738.4 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr19:2216704 G>A maps to ENST00000221482 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr19:2216704 G>A maps to ENST00000221482 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr2:69240636 C>T maps to NM_032208.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr2:69240636 C>T maps to NM_032208.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr20:43851862 T>A maps to NM_003008.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr20:43851862 T>A maps to NM_003008.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr20:61910292 G>A maps to NM_175609.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr20:61910292 G>A maps to NM_175609.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr4:995271 G>A maps to NM_000203.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr4:995271 G>A maps to NM_000203.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr4:148545073 A>G maps to NM_018241.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr4:148545073 A>G maps to NM_018241.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr6:6145962 G>A maps to NM_000129.3 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr6:6145962 G>A maps to NM_000129.3 C696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr7:2644609 A>G maps to NM_152558.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr7:2644609 A>G maps to NM_152558.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr7:63538419 C>T maps to NM_001159522.1 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-1806-01A-02D-1845-08 chr7:63538419 C>T maps to NM_001159522.1 N331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:26507076 C>T maps to ENST00000374253 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:26507076 C>T maps to ENST00000374253 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:35227181 C>T maps to NM_153212.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:35227181 C>T maps to NM_153212.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:70505049 C>T maps to NM_020794.2 Y1143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:70505049 C>T maps to NM_020794.2 Y1143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:117603104 C>T maps to NM_003594.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:117603104 C>T maps to NM_003594.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:154294515 C>T maps to NM_080429.2 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:154294515 C>T maps to NM_080429.2 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:240071078 C>T maps to NM_000740.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr1:240071078 C>T maps to NM_000740.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr11:47307121 G>A maps to NM_003682.3 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr11:47307121 G>A maps to NM_003682.3 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr11:56019878 C>A maps to NM_001004747.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr11:56019878 C>A maps to NM_001004747.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr11:65482150 C>T maps to NM_182710.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr11:65482150 C>T maps to NM_182710.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr14:88478072 C>T maps to NM_003608.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr14:88478072 C>T maps to NM_003608.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr16:21995749 G>A maps to ENST00000424898 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr16:21995749 G>A maps to ENST00000424898 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr16:28515111 C>T maps to NM_145659.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr16:28515111 C>T maps to NM_145659.3 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr17:5286436 G>A maps to NM_004703.4 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr17:5286436 G>A maps to NM_004703.4 R836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr19:10655708 T>G maps to NM_032885.4 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr19:10655708 T>G maps to NM_032885.4 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:109410996 T>C maps to NM_144978.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:109410996 T>C maps to NM_144978.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:130877734 G>A maps to NM_001099771.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:130877734 G>A maps to NM_001099771.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:141986958 C>A maps to NM_018557.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:141986958 C>A maps to NM_018557.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:198949320 C>T maps to NM_006226.3 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr2:198949320 C>T maps to NM_006226.3 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr20:23383672 A>T maps to ENST00000431864 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr20:23383672 A>T maps to ENST00000431864 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr22:30857618 G>A maps to NM_174975.4 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr22:30857618 G>A maps to NM_174975.4 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr3:102157372 G>A maps to NM_175056.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr3:102157372 G>A maps to NM_175056.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr6:27368166 G>A maps to NM_001076781.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr6:27368166 G>A maps to NM_001076781.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr6:47846893 G>A maps to NM_001013732.3 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr6:47846893 G>A maps to NM_001013732.3 N562N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr6:134493393 G>A maps to NM_001143676.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr6:134493393 G>A maps to NM_001143676.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr7:50467931 C>T maps to NM_006060.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr7:50467931 C>T maps to NM_006060.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr7:98257874 C>T maps to NM_002523.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2557-01A-01D-1494-08 chr7:98257874 C>T maps to NM_002523.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:47264923 T>C maps to NM_001099772.1 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:47264923 T>C maps to NM_001099772.1 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:55166994 C>T maps to ENST00000454855 D1124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:55166994 C>T maps to ENST00000454855 D1124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:209773438 G>A maps to NM_020439.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:209773438 G>A maps to NM_020439.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:228345794 C>T maps to NM_020435.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr1:228345794 C>T maps to NM_020435.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr11:64001431 C>T maps to NM_005528.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr11:64001431 C>T maps to NM_005528.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr11:92533805 C>T maps to ENST00000298047 R2543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr11:92533805 C>T maps to ENST00000298047 R2543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr11:99690431 G>T maps to NM_014361.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr11:99690431 G>T maps to NM_014361.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr12:70949923 A>G maps to NM_001109754.1 P1573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr12:70949923 A>G maps to NM_001109754.1 P1573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr14:44974609 A>T maps to NM_032135.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr14:44974609 A>T maps to NM_032135.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr14:62536339 C>T maps to NM_031914.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr14:62536339 C>T maps to NM_031914.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr16:27441406 G>A maps to NM_181079.4 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr16:27441406 G>A maps to NM_181079.4 W27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr19:1083207 G>A maps to NM_012292.2 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr19:1083207 G>A maps to NM_012292.2 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr19:13035594 G>A maps to NM_004461.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr19:13035594 G>A maps to NM_004461.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr2:43802135 C>T maps to ENST00000330266 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr2:43802135 C>T maps to ENST00000330266 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr2:230724205 C>T maps to ENST00000389044 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr2:230724205 C>T maps to ENST00000389044 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr20:17434508 C>T maps to NM_002594.2 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr20:17434508 C>T maps to NM_002594.2 N336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr3:33584994 G>A maps to ENST00000359576 R1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr3:33584994 G>A maps to ENST00000359576 R1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr3:57646540 A>G maps to NM_152678.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr3:57646540 A>G maps to NM_152678.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr5:148929729 C>T maps to NM_001025105.1 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr5:148929729 C>T maps to NM_001025105.1 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr6:7569462 C>T maps to NM_004415.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr6:7569462 C>T maps to NM_004415.2 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr6:55113581 A>G maps to NM_001526.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr6:55113581 A>G maps to NM_001526.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr7:43485122 G>A maps to NM_015052.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr7:43485122 G>A maps to NM_015052.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr7:80091826 G>A maps to NM_001102386.1 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr7:80091826 G>A maps to NM_001102386.1 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr8:1871954 G>A maps to ENST00000398564 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr8:1871954 G>A maps to ENST00000398564 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr8:124206322 C>T maps to NM_032899.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr8:124206322 C>T maps to NM_032899.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr9:107332230 G>A maps to NM_001004483.1 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chr9:107332230 G>A maps to NM_001004483.1 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:15509314 C>T maps to NM_003662.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:15509314 C>T maps to NM_003662.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:39921625 T>C maps to NM_001123385.1 R1398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:39921625 T>C maps to NM_001123385.1 R1398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:50134484 A>C maps to NM_001013742.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:50134484 A>C maps to NM_001013742.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:72433529 T>A maps to NM_021963.2 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:72433529 T>A maps to NM_021963.2 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:119410874 G>A maps to NM_017938.3 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2558-01A-01D-1494-08 chrX:119410874 G>A maps to NM_017938.3 Y204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr1:152192835 A>G maps to NM_001009931.1 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr1:152192835 A>G maps to NM_001009931.1 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr10:37506709 G>A maps to ENST00000374660 E1120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr10:37506709 G>A maps to ENST00000374660 E1120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr10:72495038 C>T maps to NM_139155.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr10:72495038 C>T maps to NM_139155.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr12:58125705 C>T maps to NM_001122772.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr12:58125705 C>T maps to NM_001122772.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr13:21331635 G>A maps to NM_174928.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr13:21331635 G>A maps to NM_174928.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr14:24109022 C>T maps to NM_182908.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr14:24109022 C>T maps to NM_182908.4 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:603458 C>T maps to NM_005632.2 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:603458 C>T maps to NM_005632.2 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:21698816 C>T maps to ENST00000286149 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:21698816 C>T maps to ENST00000286149 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:31409189 G>A maps to ENST00000444228 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:31409189 G>A maps to ENST00000444228 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:57054710 C>T maps to NM_032206.3 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr16:57054710 C>T maps to NM_032206.3 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr17:10213132 G>A maps to NM_003802.2 H1557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr17:10213132 G>A maps to NM_003802.2 H1557H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr17:38936089 C>T maps to NM_181537.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr17:38936089 C>T maps to NM_181537.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr17:56599395 C>A maps to NM_004574.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr17:56599395 C>A maps to NM_004574.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr19:6928179 G>A maps to ENST00000381407 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr19:6928179 G>A maps to ENST00000381407 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr2:33335816 G>A maps to ENST00000354476 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr2:33335816 G>A maps to ENST00000354476 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr2:103057837 G>T did not map to a codon.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr2:103057837 G>T did not map to a codon.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr2:170101419 C>T maps to NM_004525.2 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr2:170101419 C>T maps to NM_004525.2 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr22:37524495 G>T maps to ENST00000406505 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr22:37524495 G>T maps to ENST00000406505 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr3:194062678 G>A maps to NM_001080513.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr3:194062678 G>A maps to NM_001080513.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr4:47405591 G>T maps to NM_000812.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr4:47405591 G>T maps to NM_000812.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:43040057 C>A maps to NM_001014279.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:43040057 C>A maps to NM_001014279.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:89989725 C>T maps to NM_032119.3 L2385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:89989725 C>T maps to NM_032119.3 L2385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:127728840 G>T maps to NM_001999.3 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:127728840 G>T maps to NM_001999.3 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:140768968 C>T maps to NM_003736.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr5:140768968 C>T maps to NM_003736.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr6:34827264 G>A maps to NM_017754.3 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr6:34827264 G>A maps to NM_017754.3 V1044V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr8:1871716 G>A maps to ENST00000398564 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chr8:1871716 G>A maps to ENST00000398564 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chrX:39923054 C>T maps to NM_001123385.1 W1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chrX:39923054 C>T maps to NM_001123385.1 W1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chrX:70680611 C>T maps to ENST00000449580 D1819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chrX:70680611 C>T maps to ENST00000449580 D1819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chrX:83128393 G>A maps to NM_021118.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2559-01A-01D-1494-08 chrX:83128393 G>A maps to NM_021118.1 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr1:179304792 G>C did not map to a codon.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr1:179304792 G>C did not map to a codon.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr11:64575551 G>A maps to NM_130804.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr11:64575551 G>A maps to NM_130804.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr11:92715285 C>T maps to NM_005959.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr11:92715285 C>T maps to NM_005959.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr15:90802039 C>T maps to ENST00000438251 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr15:90802039 C>T maps to ENST00000438251 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr17:37431296 G>T maps to NM_032875.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr17:37431296 G>T maps to NM_032875.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr3:9055067 C>A maps to NM_014850.2 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr3:9055067 C>A maps to NM_014850.2 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr4:57189556 C>T maps to NM_020722.1 Q1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr4:57189556 C>T maps to NM_020722.1 Q1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr5:160063303 C>T maps to NM_025153.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr5:160063303 C>T maps to NM_025153.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr8:22106785 C>T maps to NM_001722.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr8:22106785 C>T maps to NM_001722.2 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr9:125391090 G>A maps to NM_001004450.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chr9:125391090 G>A maps to NM_001004450.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chrX:51239119 G>A maps to NM_018159.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2561-01A-02D-1494-08 chrX:51239119 G>A maps to NM_018159.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr1:16093946 G>A maps to NM_017556.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr1:16093946 G>A maps to NM_017556.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr1:111494469 G>A maps to NM_018372.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr1:111494469 G>A maps to NM_018372.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr1:159162381 C>T maps to NM_021189.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr1:159162381 C>T maps to NM_021189.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr10:98808847 G>A maps to NM_003061.2 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr10:98808847 G>A maps to NM_003061.2 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr11:60183619 C>T maps to NM_032597.3 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr11:60183619 C>T maps to NM_032597.3 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr11:68177524 G>A maps to NM_002335.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr11:68177524 G>A maps to NM_002335.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr12:129558524 G>A maps to NM_133448.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr12:129558524 G>A maps to NM_133448.2 I1065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr13:111134944 C>T maps to NM_001846.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr13:111134944 C>T maps to NM_001846.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr15:89421299 C>T maps to NM_178232.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr15:89421299 C>T maps to NM_178232.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr17:63173875 C>T maps to NM_003835.3 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr17:63173875 C>T maps to NM_003835.3 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr18:63489428 A>G maps to NM_004361.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr18:63489428 A>G maps to NM_004361.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr19:35804317 G>A maps to NM_002361.3 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr19:35804317 G>A maps to NM_002361.3 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr19:50392980 T>G maps to NM_172374.1 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr19:50392980 T>G maps to NM_172374.1 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr20:57599543 C>T maps to NM_030773.3 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr20:57599543 C>T maps to NM_030773.3 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr3:98002585 C>T maps to NM_001005482.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr3:98002585 C>T maps to NM_001005482.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr3:134967276 G>A maps to NM_004441.4 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr3:134967276 G>A maps to NM_004441.4 A872A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr4:864619 C>T maps to NM_005255.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr4:864619 C>T maps to NM_005255.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr5:156186310 C>T maps to NM_000337.5 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr5:156186310 C>T maps to NM_000337.5 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr6:1930435 G>A maps to NM_001500.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr6:1930435 G>A maps to NM_001500.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr6:106764058 G>A maps to NM_004849.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr6:106764058 G>A maps to NM_004849.2 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr7:128415496 T>A maps to NM_001708.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr7:128415496 T>A maps to NM_001708.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr7:138854078 A>G maps to NM_024926.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr7:138854078 A>G maps to NM_024926.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr9:71606124 C>T maps to NM_003558.2 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr9:71606124 C>T maps to NM_003558.2 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr9:112694259 C>T maps to NM_007203.4 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2562-01A-01D-1494-08 chr9:112694259 C>T maps to NM_007203.4 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr1:36028234 G>A did not map to a codon.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr1:36028234 G>A did not map to a codon.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr1:39876293 G>A maps to NM_015038.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr1:39876293 G>A maps to NM_015038.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr1:228645126 C>T maps to NM_033445.2 *131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr1:228645126 C>T maps to NM_033445.2 *131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr11:61048378 C>T maps to NM_152718.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr11:61048378 C>T maps to NM_152718.2 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr12:6463924 G>T maps to NM_001159576.1 Y470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr12:6463924 G>T maps to NM_001159576.1 Y470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr12:53343220 C>T maps to NM_000224.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr12:53343220 C>T maps to NM_000224.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr12:71094984 G>T maps to NM_002849.2 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr12:71094984 G>T maps to NM_002849.2 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr13:114502322 C>G maps to NM_182614.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr13:114502322 C>G maps to NM_182614.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr15:42106768 G>A maps to NM_001128608.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr15:42106768 G>A maps to NM_001128608.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr17:7404278 G>A maps to NM_000937.4 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr17:7404278 G>A maps to NM_000937.4 E634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr17:48614387 G>A maps to NM_017957.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr17:48614387 G>A maps to NM_017957.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr19:50945480 C>A maps to NM_004533.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr19:50945480 C>A maps to NM_004533.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr2:112608406 T>A maps to NM_022662.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr2:112608406 T>A maps to NM_022662.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr2:230663733 T>C maps to ENST00000389044 K1086K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr2:230663733 T>C maps to ENST00000389044 K1086K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr22:50280048 C>T maps to NM_014838.2 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr22:50280048 C>T maps to NM_014838.2 S913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr5:168212915 G>A maps to NM_003062.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr5:168212915 G>A maps to NM_003062.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr6:155572048 A>C maps to ENST00000456144 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr6:155572048 A>C maps to ENST00000456144 V1347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr7:50121432 G>A maps to NM_007009.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr7:50121432 G>A maps to NM_007009.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr8:113988285 A>T maps to NM_198123.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chr8:113988285 A>T maps to NM_198123.1 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:108673541 G>A maps to ENST00000218006 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:108673541 G>A maps to ENST00000218006 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:119565294 G>A maps to NM_002294.2 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:119565294 G>A maps to NM_002294.2 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:122532506 C>T maps to NM_000828.4 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:122532506 C>T maps to NM_000828.4 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:128657224 G>A maps to NM_003069.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:128657224 G>A maps to NM_003069.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:140995643 C>T maps to NM_005462.4 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2563-01A-01D-1494-08 chrX:140995643 C>T maps to NM_005462.4 P818P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr1:89525903 G>A maps to NM_002053.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr1:89525903 G>A maps to NM_002053.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr1:145440908 C>T maps to NM_006472.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr1:145440908 C>T maps to NM_006472.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr11:89531693 G>A maps to NM_020358.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr11:89531693 G>A maps to NM_020358.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr12:85492268 C>T maps to NM_001079910.1 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr12:85492268 C>T maps to NM_001079910.1 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr12:133732278 A>G maps to NM_015394.4 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr12:133732278 A>G maps to NM_015394.4 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr14:19566059 C>G maps to NM_001005356.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr14:19566059 C>G maps to NM_001005356.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr14:24801071 G>A maps to NM_139247.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr14:24801071 G>A maps to NM_139247.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr15:74564063 C>T maps to ENST00000321288 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr15:74564063 C>T maps to ENST00000321288 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr16:31374347 C>T maps to NM_000887.3 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr16:31374347 C>T maps to NM_000887.3 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr17:7187696 G>A maps to NM_001042.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr17:7187696 G>A maps to NM_001042.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr17:12666834 G>A maps to NM_001146312.1 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr17:12666834 G>A maps to NM_001146312.1 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr17:21319340 C>T maps to NM_021012.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr17:21319340 C>T maps to NM_021012.4 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr19:2933837 C>T maps to NM_021217.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr19:2933837 C>T maps to NM_021217.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr19:31767725 G>A maps to NM_020856.2 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr19:31767725 G>A maps to NM_020856.2 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr2:18765377 C>T maps to ENST00000455492 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr2:18765377 C>T maps to ENST00000455492 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr2:128707446 G>C maps to NM_001145928.1 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr2:128707446 G>C maps to NM_001145928.1 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr22:40080362 G>T maps to NM_021096.3 E1963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr22:40080362 G>T maps to NM_021096.3 E1963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr3:45814089 C>T maps to NM_020208.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr3:45814089 C>T maps to NM_020208.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr3:172165996 C>T maps to NM_198407.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr3:172165996 C>T maps to NM_198407.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr4:70599913 A>G maps to NM_014465.3 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr4:70599913 A>G maps to NM_014465.3 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr7:24742378 C>T maps to NM_001127453.1 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr7:24742378 C>T maps to NM_001127453.1 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr7:150921936 G>A maps to NM_005692.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr7:150921936 G>A maps to NM_005692.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr9:97333779 G>A maps to NM_003837.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr9:97333779 G>A maps to NM_003837.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr9:98669531 T>G maps to NM_001010895.2 L267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr9:98669531 T>G maps to NM_001010895.2 L267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr9:127262848 C>T maps to NM_004959.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2564-01A-01D-1494-08 chr9:127262848 C>T maps to NM_004959.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr1:3756340 C>T did not map to a codon.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr1:3756340 C>T did not map to a codon.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr1:70611581 T>C maps to NM_017768.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr1:70611581 T>C maps to NM_017768.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr1:156497821 C>T maps to NM_178229.4 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr1:156497821 C>T maps to NM_178229.4 P1568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr10:22617608 C>T maps to NM_005180.6 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr10:22617608 C>T maps to NM_005180.6 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr10:102697208 A>G maps to NM_001136123.1 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr10:102697208 A>G maps to NM_001136123.1 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr12:117655933 G>A maps to ENST00000338101 V1436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr12:117655933 G>A maps to ENST00000338101 V1436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr17:38938700 G>A maps to NM_181537.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr17:38938700 G>A maps to NM_181537.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr2:33482447 A>G maps to ENST00000354476 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr2:33482447 A>G maps to ENST00000354476 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr2:149866822 C>A maps to NM_004522.1 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr2:149866822 C>A maps to NM_004522.1 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr20:44431986 C>A maps to NM_052951.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr20:44431986 C>A maps to NM_052951.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr21:43539378 C>T maps to NM_173568.3 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr21:43539378 C>T maps to NM_173568.3 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr4:88987001 C>T maps to NM_000297.2 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr4:88987001 C>T maps to NM_000297.2 Q777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr5:17275819 C>T maps to NM_006317.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr5:17275819 C>T maps to NM_006317.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr5:140711984 G>A maps to NM_018912.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr5:140711984 G>A maps to NM_018912.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr7:66482861 G>A maps to NM_018264.2 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr7:66482861 G>A maps to NM_018264.2 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr7:80290462 C>T maps to NM_001127444.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr7:80290462 C>T maps to NM_001127444.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr8:55537453 C>T maps to NM_006269.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chr8:55537453 C>T maps to NM_006269.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chrX:135301830 C>T did not map to a codon.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chrX:135301830 C>T did not map to a codon.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chrX:148038124 G>A maps to NM_002025.3 K850K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2565-01A-01D-1494-08 chrX:148038124 G>A maps to NM_002025.3 K850K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr1:89655828 C>T maps to NM_052941.4 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr1:89655828 C>T maps to NM_052941.4 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr1:248308934 G>A maps to NM_001004690.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr1:248308934 G>A maps to NM_001004690.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr10:79581859 C>G did not map to a codon.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr10:79581859 C>G did not map to a codon.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr11:6589083 T>G maps to NM_144666.2 Y4115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr11:6589083 T>G maps to NM_144666.2 Y4115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr11:121444998 G>A maps to NM_003105.5 G1129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr11:121444998 G>A maps to NM_003105.5 G1129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr12:100711648 C>T maps to NM_017988.4 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr12:100711648 C>T maps to NM_017988.4 N447N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr16:3187508 C>T maps to NM_001134655.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr16:3187508 C>T maps to NM_001134655.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr16:30960834 C>T maps to NM_152288.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr16:30960834 C>T maps to NM_152288.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr16:75563754 C>T maps to NM_024533.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr16:75563754 C>T maps to NM_024533.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr17:16593761 G>A maps to NM_014695.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr17:16593761 G>A maps to NM_014695.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr18:28934951 C>T maps to NM_001942.2 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr18:28934951 C>T maps to NM_001942.2 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr19:10659589 G>A maps to NM_032885.4 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr19:10659589 G>A maps to NM_032885.4 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr19:42558501 G>A maps to NM_002088.3 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr19:42558501 G>A maps to NM_002088.3 H342H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr19:54466518 T>G maps to NM_031895.5 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr19:54466518 T>G maps to NM_031895.5 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr2:128177526 G>A maps to ENST00000409048 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr2:128177526 G>A maps to ENST00000409048 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr21:44296864 G>A maps to NM_018669.4 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr21:44296864 G>A maps to NM_018669.4 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr3:47619239 C>T maps to ENST00000383738 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr3:47619239 C>T maps to ENST00000383738 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr3:121647353 G>T maps to NM_021082.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr3:121647353 G>T maps to NM_021082.3 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr3:139098009 G>A maps to NM_004766.2 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr3:139098009 G>A maps to NM_004766.2 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr4:100130079 A>G maps to NM_001102470.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr4:100130079 A>G maps to NM_001102470.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr6:139694946 C>T maps to NM_006079.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr6:139694946 C>T maps to NM_006079.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr7:37934141 C>T maps to NM_016616.4 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr7:37934141 C>T maps to NM_016616.4 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr7:51096734 T>C maps to ENST00000395542 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr7:51096734 T>C maps to ENST00000395542 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr7:53104083 C>T maps to NM_182595.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr7:53104083 C>T maps to NM_182595.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr8:119391928 C>T maps to NM_207506.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr8:119391928 C>T maps to NM_207506.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr9:136508596 C>T maps to NM_000787.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chr9:136508596 C>T maps to NM_000787.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chrX:10096665 G>T maps to NM_015691.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2567-01A-01D-1494-08 chrX:10096665 G>T maps to NM_015691.3 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr1:228511260 G>A maps to NM_001098623.1 E5202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr1:228511260 G>A maps to NM_001098623.1 E5202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr12:66547226 G>A maps to ENST00000286424 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr12:66547226 G>A maps to ENST00000286424 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr17:34073120 G>A maps to NM_139285.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr17:34073120 G>A maps to NM_139285.2 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr20:23065722 G>A maps to NM_012072.3 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr20:23065722 G>A maps to NM_012072.3 C369C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr3:111766625 T>G maps to ENST00000443106 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr3:111766625 T>G maps to ENST00000443106 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr6:70916650 G>A maps to NM_001858.4 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr6:70916650 G>A maps to NM_001858.4 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr7:4153058 G>T maps to NM_152744.3 R1191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr7:4153058 G>T maps to NM_152744.3 R1191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr7:28319006 T>A did not map to a codon.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr7:28319006 T>A did not map to a codon.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr9:140074734 C>A maps to NM_013366.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2569-01A-01D-1494-08 chr9:140074734 C>A maps to NM_013366.3 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr1:248059604 C>T maps to NM_001001957.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr1:248059604 C>T maps to NM_001001957.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr11:45945055 T>C maps to NM_152312.3 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr11:45945055 T>C maps to NM_152312.3 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr11:64064378 G>A maps to ENST00000422670 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr11:64064378 G>A maps to ENST00000422670 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr2:152322630 T>C maps to NM_018151.4 N2199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr2:152322630 T>C maps to NM_018151.4 N2199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr2:242423743 C>T maps to NM_014808.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr2:242423743 C>T maps to NM_014808.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr20:60504709 C>T maps to NM_001794.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr20:60504709 C>T maps to NM_001794.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr3:189681755 A>G maps to NM_018192.3 Y675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr3:189681755 A>G maps to NM_018192.3 Y675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr5:45695973 G>C maps to NM_021072.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr5:45695973 G>C maps to NM_021072.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr5:56177897 A>G maps to NM_005921.1 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr5:56177897 A>G maps to NM_005921.1 Q957Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr6:39285600 G>A maps to NM_032115.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr6:39285600 G>A maps to NM_032115.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr7:87069033 C>T maps to NM_018849.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-2570-01A-01D-1495-08 chr7:87069033 C>T maps to NM_018849.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr1:152325023 T>C maps to NM_001014342.2 G1746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr1:152325023 T>C maps to NM_001014342.2 G1746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr1:169698773 G>A maps to NM_000450.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr1:169698773 G>A maps to NM_000450.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr10:127462499 C>T maps to NM_147191.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr10:127462499 C>T maps to NM_147191.1 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr16:55525752 C>T maps to NM_004530.4 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr16:55525752 C>T maps to NM_004530.4 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr17:9822944 A>G maps to NM_201433.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr17:9822944 A>G maps to NM_201433.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr17:29587503 G>A maps to NM_001042492.2 E1516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr17:29587503 G>A maps to NM_001042492.2 E1516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr19:9088856 T>A maps to NM_024690.2 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr19:9088856 T>A maps to NM_024690.2 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr2:27459351 C>T maps to NM_004341.3 P1425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr2:27459351 C>T maps to NM_004341.3 P1425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr2:37078197 C>T maps to NM_003162.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr2:37078197 C>T maps to NM_003162.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr2:202252531 G>A maps to NM_015049.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr2:202252531 G>A maps to NM_015049.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr3:38770173 G>A maps to NM_006514.2 H833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr3:38770173 G>A maps to NM_006514.2 H833H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr3:138739095 G>A maps to NM_001013650.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr3:138739095 G>A maps to NM_001013650.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr5:151125915 T>C maps to NM_004045.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr5:151125915 T>C maps to NM_004045.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr7:64864754 C>A maps to NM_152626.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr7:64864754 C>A maps to NM_152626.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr8:75171692 C>T maps to NM_020647.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr8:75171692 C>T maps to NM_020647.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr8:95262753 C>T maps to NM_181702.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5408-01A-01D-1696-08 chr8:95262753 C>T maps to NM_181702.2 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr1:169772374 C>T maps to NM_018186.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr1:169772374 C>T maps to NM_018186.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr10:79566616 C>A maps to NM_004747.3 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr10:79566616 C>A maps to NM_004747.3 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr11:58602090 G>A maps to NM_145016.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr11:58602090 G>A maps to NM_145016.3 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr11:70279265 G>A maps to NM_001184740.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr11:70279265 G>A maps to NM_001184740.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr11:103014113 C>T maps to NM_001080463.1 R898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr11:103014113 C>T maps to NM_001080463.1 R898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr12:12232400 C>T maps to NM_138722.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr12:12232400 C>T maps to NM_138722.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr12:56330334 G>A maps to NM_201554.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr12:56330334 G>A maps to NM_201554.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr14:21871324 G>A maps to NM_001170629.1 Q1189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr14:21871324 G>A maps to NM_001170629.1 Q1189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr17:29533303 C>A maps to NM_001042492.2 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr17:29533303 C>A maps to NM_001042492.2 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr19:16034747 G>A maps to NM_021187.3 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr19:16034747 G>A maps to NM_021187.3 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr19:54503002 A>G maps to NM_145814.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr19:54503002 A>G maps to NM_145814.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr22:32937633 G>A maps to NM_003490.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr22:32937633 G>A maps to NM_003490.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr3:191179073 C>T maps to NM_001083308.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr3:191179073 C>T maps to NM_001083308.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr4:39116787 C>G maps to NM_015990.4 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr4:39116787 C>G maps to NM_015990.4 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr4:90170301 C>T maps to NM_198281.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr4:90170301 C>T maps to NM_198281.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr5:176301526 C>T maps to NM_133369.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chr5:176301526 C>T maps to NM_133369.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:2407461 C>T maps to NM_004729.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:2407461 C>T maps to NM_004729.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:24073153 G>A maps to NM_001415.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:24073153 G>A maps to NM_001415.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:54276525 G>A maps to NM_020922.4 R872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:54276525 G>A maps to NM_020922.4 R872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:105011567 C>T maps to NM_017416.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5410-01A-01D-1696-08 chrX:105011567 C>T maps to NM_017416.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr1:247695276 A>G maps to NM_198074.4 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr1:247695276 A>G maps to NM_198074.4 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr11:59271633 G>T maps to NM_001004706.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr11:59271633 G>T maps to NM_001004706.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr12:81101719 C>T maps to NM_002469.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr12:81101719 C>T maps to NM_002469.2 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr18:57014767 A>G maps to NM_005570.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr18:57014767 A>G maps to NM_005570.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr2:74729803 G>A maps to NM_001009812.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr2:74729803 G>A maps to NM_001009812.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr2:75720688 G>A maps to NM_032181.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr2:75720688 G>A maps to NM_032181.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr2:204260427 C>T maps to ENST00000295851 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr2:204260427 C>T maps to ENST00000295851 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr21:32639087 G>C maps to NM_003253.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr21:32639087 G>C maps to NM_003253.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr21:45953584 G>A maps to ENST00000443468 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr21:45953584 G>A maps to ENST00000443468 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr3:143212495 T>C maps to NM_173653.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr3:143212495 T>C maps to NM_173653.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr4:55597496 C>T maps to NM_000222.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr4:55597496 C>T maps to NM_000222.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr4:71346616 A>G maps to NM_152291.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr4:71346616 A>G maps to NM_152291.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr7:21784531 C>T maps to NM_003777.3 C2794C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr7:21784531 C>T maps to NM_003777.3 C2794C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr8:30695498 C>T maps to NM_031271.3 T2384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5411-01A-01D-1696-08 chr8:30695498 C>T maps to NM_031271.3 T2384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:10713866 C>T maps to NM_001079843.1 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:10713866 C>T maps to NM_001079843.1 A749A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:54059815 G>A maps to NM_147193.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:54059815 G>A maps to NM_147193.2 R254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:145532130 C>T maps to NM_003637.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:145532130 C>T maps to NM_003637.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:153923903 G>A maps to NM_181715.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:153923903 G>A maps to NM_181715.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:228362895 C>T maps to NM_001010867.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:228362895 C>T maps to NM_001010867.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:248685051 C>T maps to NM_001013355.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr1:248685051 C>T maps to NM_001013355.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr11:123485468 G>A maps to ENST00000456860 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr11:123485468 G>A maps to ENST00000456860 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr16:57688008 C>T maps to NM_005682.5 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr16:57688008 C>T maps to NM_005682.5 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr17:39637190 T>A maps to NM_002280.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr17:39637190 T>A maps to NM_002280.4 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr18:9570481 G>A maps to NM_001042388.1 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr18:9570481 G>A maps to NM_001042388.1 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr19:14627499 T>C maps to NM_006145.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr19:14627499 T>C maps to NM_006145.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr2:128484319 C>T maps to NM_018383.4 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr2:128484319 C>T maps to NM_018383.4 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr2:176981725 G>A maps to NM_002148.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr2:176981725 G>A maps to NM_002148.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr2:238738021 G>A maps to NM_001080504.2 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr2:238738021 G>A maps to NM_001080504.2 S922S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr20:45315630 C>A maps to NM_033550.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr20:45315630 C>A maps to NM_033550.3 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr3:12858461 C>T maps to NM_001162499.1 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr3:12858461 C>T maps to NM_001162499.1 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr5:158140122 G>A maps to NM_024007.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr5:158140122 G>A maps to NM_024007.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr7:44611161 C>A maps to NM_019082.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr7:44611161 C>A maps to NM_019082.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr7:74212398 C>T maps to NM_173537.2 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr7:74212398 C>T maps to NM_173537.2 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chr9:124062284 T>G did not map to a codon.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chrX:41075423 G>A maps to NM_001039590.2 V1868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chrX:41075423 G>A maps to NM_001039590.2 V1868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chrX:135291465 C>T maps to NM_001159702.2 H251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chrX:135291465 C>T maps to NM_001159702.2 H251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chrX:144905001 T>C maps to NM_001144010.2 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5412-01A-01D-1696-08 chrX:144905001 T>C maps to NM_001144010.2 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr1:248637274 C>A maps to NM_001005495.1 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr1:248637274 C>A maps to NM_001005495.1 C208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr19:38103380 G>A maps to NM_152606.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr19:38103380 G>A maps to NM_152606.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:21228711 G>A maps to NM_000384.2 I3676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:21228711 G>A maps to NM_000384.2 I3676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:65296847 C>A maps to NM_015147.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:65296847 C>A maps to NM_015147.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:165997259 T>C maps to NM_006922.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:165997259 T>C maps to NM_006922.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:198570302 G>A maps to NM_138395.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr2:198570302 G>A maps to NM_138395.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr3:45800487 G>A maps to NM_020208.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr3:45800487 G>A maps to NM_020208.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr3:52525479 G>A maps to NM_007184.3 P1285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr3:52525479 G>A maps to NM_007184.3 P1285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr3:57132317 C>T maps to NM_017563.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr3:57132317 C>T maps to NM_017563.3 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr4:87028498 C>T maps to NM_138982.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr4:87028498 C>T maps to NM_138982.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr4:128807277 A>T maps to NM_014264.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr4:128807277 A>T maps to NM_014264.4 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr5:33549383 G>A maps to NM_030955.2 G1410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr5:33549383 G>A maps to NM_030955.2 G1410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr5:150947261 G>A maps to NM_001447.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr5:150947261 G>A maps to NM_001447.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr6:36185727 C>T maps to NM_015695.2 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr6:36185727 C>T maps to NM_015695.2 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr6:63990384 G>A maps to NM_016571.2 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr6:63990384 G>A maps to NM_016571.2 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr6:167704888 C>A did not map to a codon.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr6:167704888 C>A did not map to a codon.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr7:149493792 G>A maps to NM_198455.2 S2264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr7:149493792 G>A maps to NM_198455.2 S2264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr7:157046787 T>C maps to NM_014671.2 N945N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr7:157046787 T>C maps to NM_014671.2 N945N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr9:79118131 G>T maps to NM_001097636.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr9:79118131 G>T maps to NM_001097636.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr1:152187705 G>A maps to NM_001009931.1 Y2133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr1:152187705 G>A maps to NM_001009931.1 Y2133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr11:7509543 C>T maps to NM_198474.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr11:7509543 C>T maps to NM_198474.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr11:55406750 G>T maps to NM_001004124.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr11:55406750 G>T maps to NM_001004124.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr11:68206025 G>A maps to NM_002335.2 Q1408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr11:68206025 G>A maps to NM_002335.2 Q1408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr13:84455309 C>A maps to NM_052910.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr13:84455309 C>A maps to NM_052910.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr2:158300463 C>T maps to NM_004288.4 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr2:158300463 C>T maps to NM_004288.4 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr2:201434568 A>G maps to NM_152524.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr2:201434568 A>G maps to NM_152524.5 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr2:228884216 G>A maps to NM_001142644.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr2:228884216 G>A maps to NM_001142644.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr3:109050751 C>T maps to NM_018189.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr3:109050751 C>T maps to NM_018189.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr5:5190211 T>C maps to NM_139056.2 C392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr5:5190211 T>C maps to NM_139056.2 C392C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr5:156346518 G>T maps to NM_138379.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr5:156346518 G>T maps to NM_138379.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr6:44107302 C>T maps to NM_018426.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr6:44107302 C>T maps to NM_018426.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr7:99123820 G>T maps to NM_014569.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr7:99123820 G>T maps to NM_014569.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr7:142658589 T>C did not map to a codon.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr7:142658589 T>C did not map to a codon.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr8:12956044 C>T maps to NM_182643.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr8:12956044 C>T maps to NM_182643.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr8:15519786 T>G maps to NM_006765.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chr8:15519786 T>G maps to NM_006765.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chrX:21508620 G>T maps to NM_014927.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5414-01A-01D-1486-08 chrX:21508620 G>T maps to NM_014927.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:119985579 C>T did not map to a codon.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:119985579 C>T did not map to a codon.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:152188023 C>G maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:152188023 C>G maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:168165849 C>A maps to NM_152902.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:168165849 C>A maps to NM_152902.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:226027610 C>T maps to NM_001136018.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr1:226027610 C>T maps to NM_001136018.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr10:27964298 C>T maps to NM_173576.2 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr10:27964298 C>T maps to NM_173576.2 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr11:125787055 C>T maps to NM_013264.3 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr11:125787055 C>T maps to NM_013264.3 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr12:26864180 G>A maps to NM_002223.2 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr12:26864180 G>A maps to NM_002223.2 C292C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr12:130015731 G>A maps to NM_133448.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr12:130015731 G>A maps to NM_133448.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr15:65489344 G>T maps to NM_003613.3 G1093G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr15:65489344 G>T maps to NM_003613.3 G1093G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr15:91835640 C>T maps to NM_014848.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr15:91835640 C>T maps to NM_014848.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr16:822700 G>A maps to NM_001025190.1 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr16:822700 G>A maps to NM_001025190.1 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr17:7671484 C>T maps to NM_020877.2 R1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr17:7671484 C>T maps to NM_020877.2 R1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr18:28913590 C>T maps to NM_001942.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr18:28913590 C>T maps to NM_001942.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:8996489 A>G maps to NM_024690.2 P13694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:8996489 A>G maps to NM_024690.2 P13694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:15571921 A>G maps to NM_022904.1 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:15571921 A>G maps to NM_022904.1 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:46056783 C>T maps to NM_025136.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:46056783 C>T maps to NM_025136.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:55450815 G>A maps to ENST00000446217 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr19:55450815 G>A maps to ENST00000446217 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr20:36932645 C>T maps to NM_001725.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr20:36932645 C>T maps to NM_001725.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr4:81952455 G>A maps to NM_001201.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr4:81952455 G>A maps to NM_001201.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr4:166915600 C>T maps to ENST00000507499 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr4:166915600 C>T maps to ENST00000507499 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr5:76640734 A>G maps to NM_003719.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr5:76640734 A>G maps to NM_003719.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr5:86659219 A>G maps to NM_002890.1 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr5:86659219 A>G maps to NM_002890.1 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr5:135583349 G>A maps to NM_020389.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr5:135583349 G>A maps to NM_020389.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr6:45882069 G>A maps to NM_001114086.1 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr6:45882069 G>A maps to NM_001114086.1 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:89856793 C>T maps to NM_152999.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:89856793 C>T maps to NM_152999.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:128490535 A>G maps to NM_001458.4 T1799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:128490535 A>G maps to NM_001458.4 T1799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:128493856 C>T maps to NM_001458.4 I2150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:128493856 C>T maps to NM_001458.4 I2150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:138453572 G>A maps to NM_130840.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:138453572 G>A maps to NM_130840.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:142658445 C>T did not map to a codon.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr7:142658445 C>T did not map to a codon.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr8:144940596 G>A maps to NM_031308.1 P2275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5415-01A-01D-1486-08 chr8:144940596 G>A maps to NM_031308.1 P2275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr1:78338780 G>C maps to NM_198549.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr1:78338780 G>C maps to NM_198549.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr1:84408355 A>T maps to NM_024686.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr1:84408355 A>T maps to NM_024686.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr1:152326100 T>C maps to NM_001014342.2 R1387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr1:152326100 T>C maps to NM_001014342.2 R1387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr11:111166837 A>G maps to ENST00000355430 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr11:111166837 A>G maps to ENST00000355430 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr12:85450520 T>C maps to NM_001079910.1 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr12:85450520 T>C maps to NM_001079910.1 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr12:96640863 C>T maps to NM_005230.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr12:96640863 C>T maps to NM_005230.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr14:25102155 G>A maps to ENST00000382542 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr14:25102155 G>A maps to ENST00000382542 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr16:1392019 G>A maps to NM_003933.4 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr16:1392019 G>A maps to NM_003933.4 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr17:26675208 C>A maps to NM_015584.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr17:26675208 C>A maps to NM_015584.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr2:207615788 G>A maps to NM_001039845.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr2:207615788 G>A maps to NM_001039845.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr22:50615878 C>A maps to NM_052839.3 C246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr22:50615878 C>A maps to NM_052839.3 C246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr4:25819778 C>T maps to NM_015187.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr4:25819778 C>T maps to NM_015187.3 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr5:110842032 T>G maps to NM_139164.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr5:110842032 T>G maps to NM_139164.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr6:33382594 A>G maps to NM_024165.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr6:33382594 A>G maps to NM_024165.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr6:70411839 G>C maps to NM_018368.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr6:70411839 G>C maps to NM_018368.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr6:152737568 A>G maps to NM_182961.2 T2001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chr6:152737568 A>G maps to NM_182961.2 T2001T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chrX:67943637 C>G maps to NM_001142503.2 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chrX:67943637 C>G maps to NM_001142503.2 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chrX:107840791 A>G maps to ENST00000328300 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5417-01A-01D-1486-08 chrX:107840791 A>G maps to ENST00000328300 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr10:6265942 C>T maps to NM_004566.3 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr10:6265942 C>T maps to NM_004566.3 C412C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr11:62434123 T>C maps to NM_001043229.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr11:62434123 T>C maps to NM_001043229.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr12:58120987 G>A maps to NM_001122772.1 R1035R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr12:58120987 G>A maps to NM_001122772.1 R1035R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr17:40945617 C>T maps to NM_032387.4 N722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr17:40945617 C>T maps to NM_032387.4 N722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr19:6495885 G>A maps to NM_006087.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr19:6495885 G>A maps to NM_006087.2 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr2:44065791 G>A maps to NM_022436.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr2:44065791 G>A maps to NM_022436.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr2:54856718 G>A maps to NM_003128.2 E816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr2:54856718 G>A maps to NM_003128.2 E816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr2:166627132 T>C maps to NM_004482.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr2:166627132 T>C maps to NM_004482.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr20:16337073 G>A maps to NM_024704.4 G1174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr20:16337073 G>A maps to NM_024704.4 G1174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr21:47355173 C>T maps to NM_020528.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr21:47355173 C>T maps to NM_020528.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr3:9799490 T>A maps to NM_003656.3 K318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr3:9799490 T>A maps to NM_003656.3 K318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr3:10183866 C>T maps to NM_000551.2 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr3:10183866 C>T maps to NM_000551.2 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr3:120123731 C>T maps to NM_007085.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr3:120123731 C>T maps to NM_007085.4 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr4:69973992 G>A maps to NM_001074.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr4:69973992 G>A maps to NM_001074.2 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr6:51941107 G>A maps to NM_138694.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr6:51941107 G>A maps to NM_138694.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:38471800 C>T maps to NM_001635.3 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:38471800 C>T maps to NM_001635.3 W382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:53103405 C>T maps to NM_182595.3 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:53103405 C>T maps to NM_182595.3 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:72744234 C>T maps to NM_003602.3 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:72744234 C>T maps to NM_003602.3 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:106508854 C>T maps to NM_002649.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr7:106508854 C>T maps to NM_002649.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr9:133943585 C>T maps to ENST00000355048 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr9:133943585 C>T maps to ENST00000355048 F905F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr9:137623921 A>G maps to NM_000093.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5418-01A-01D-1486-08 chr9:137623921 A>G maps to NM_000093.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr11:95580910 G>A maps to NM_016156.5 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr11:95580910 G>A maps to NM_016156.5 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr12:55759175 G>T maps to NM_001005497.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr12:55759175 G>T maps to NM_001005497.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr12:58152352 C>A maps to NM_138396.4 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr12:58152352 C>A maps to NM_138396.4 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr14:74060457 C>A maps to NM_152331.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr14:74060457 C>A maps to NM_152331.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr15:42107464 C>T maps to NM_001128608.1 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr15:42107464 C>T maps to NM_001128608.1 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr2:27799822 G>A maps to NM_032266.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr2:27799822 G>A maps to NM_032266.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr20:42973946 C>T maps to NM_178491.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr20:42973946 C>T maps to NM_178491.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr5:481702 G>A maps to NM_004174.2 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr5:481702 G>A maps to NM_004174.2 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr5:6600308 G>A maps to NM_017755.5 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr5:6600308 G>A maps to NM_017755.5 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr5:16668400 G>A maps to NM_012334.2 L2020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr5:16668400 G>A maps to NM_012334.2 L2020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr6:25726578 G>T maps to NM_170745.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr6:25726578 G>T maps to NM_170745.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr7:72413474 G>A maps to ENST00000434423 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr7:72413474 G>A maps to ENST00000434423 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr9:4679886 C>G maps to NM_017913.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5856-01A-01D-1696-08 chr9:4679886 C>G maps to NM_017913.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:3328827 C>T maps to NM_022114.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:3328827 C>T maps to NM_022114.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:6314020 G>A maps to NM_207370.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:6314020 G>A maps to NM_207370.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:27268024 C>T maps to NM_006600.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:27268024 C>T maps to NM_006600.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:111490907 G>A maps to NM_018372.3 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:111490907 G>A maps to NM_018372.3 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:169347744 C>T maps to NM_003666.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:169347744 C>T maps to NM_003666.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:214837071 C>T maps to NM_016343.3 R3094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr1:214837071 C>T maps to NM_016343.3 R3094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:26243810 C>T maps to NM_017433.4 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:26243810 C>T maps to NM_017433.4 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:86008737 G>A maps to ENST00000358110 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:86008737 G>A maps to ENST00000358110 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:95995710 C>T maps to ENST00000371380 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr10:95995710 C>T maps to ENST00000371380 R752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:16036503 C>T maps to NM_001145819.1 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:16036503 C>T maps to NM_001145819.1 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:57137379 C>A maps to NM_002559.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:57137379 C>A maps to NM_002559.2 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:126143241 C>T maps to NM_017547.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:126143241 C>T maps to NM_017547.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:130343094 G>A maps to NM_139055.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr11:130343094 G>A maps to NM_139055.2 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr12:14946749 G>A maps to NM_016312.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr12:14946749 G>A maps to NM_016312.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr12:104714973 C>T maps to NM_001093771.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr12:104714973 C>T maps to NM_001093771.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr12:132397779 G>A maps to NM_003565.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr12:132397779 G>A maps to NM_003565.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr13:33704213 G>A maps to NM_178007.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr13:33704213 G>A maps to NM_178007.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr13:111088641 C>T maps to NM_001846.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr13:111088641 C>T maps to NM_001846.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:65208865 G>A maps to ENST00000394691 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:65208865 G>A maps to ENST00000394691 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:78390915 G>A maps to NM_020421.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:78390915 G>A maps to NM_020421.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:95058443 G>A maps to NM_000624.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:95058443 G>A maps to NM_000624.4 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:103412979 C>T maps to NM_006035.3 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr14:103412979 C>T maps to NM_006035.3 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr15:28421857 C>T maps to NM_004667.4 A3163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr15:28421857 C>T maps to NM_004667.4 A3163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr15:42151138 A>G maps to ENST00000320955 H2676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr15:42151138 A>G maps to ENST00000320955 H2676H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr15:101567913 C>T maps to NM_024652.3 D866D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr15:101567913 C>T maps to NM_024652.3 D866D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr16:22926621 G>A maps to NM_006043.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr16:22926621 G>A maps to NM_006043.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr16:81236191 G>A maps to NM_052892.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr16:81236191 G>A maps to NM_052892.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:1780601 C>T maps to NM_002945.3 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:1780601 C>T maps to NM_002945.3 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:4713213 C>T maps to NM_002663.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:4713213 C>T maps to NM_002663.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:6023635 G>A maps to NM_015253.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:6023635 G>A maps to NM_015253.1 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:36704804 G>A maps to NM_025248.2 I1086I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:36704804 G>A maps to NM_025248.2 I1086I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:66246474 A>G maps to NM_016627.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:66246474 A>G maps to NM_016627.4 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:74395032 G>A maps to NM_022066.3 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:74395032 G>A maps to NM_022066.3 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:79556035 G>A maps to NM_017921.2 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr17:79556035 G>A maps to NM_017921.2 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:21136386 T>C maps to NM_000271.4 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:21136386 T>C maps to NM_000271.4 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:44036517 C>T maps to NM_152470.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:44036517 C>T maps to NM_152470.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:48252335 C>T maps to NM_002747.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:48252335 C>T maps to NM_002747.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:77624215 C>T maps to NM_012283.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr18:77624215 C>T maps to NM_012283.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:6222503 C>T maps to NM_005934.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:6222503 C>T maps to NM_005934.3 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:10886406 G>A maps to NM_001005361.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:10886406 G>A maps to NM_001005361.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:19356150 G>A maps to NM_004386.2 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:19356150 G>A maps to NM_004386.2 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:38590639 G>A maps to NM_015073.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:38590639 G>A maps to NM_015073.1 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:41009786 C>T maps to NM_020971.2 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:41009786 C>T maps to NM_020971.2 H471H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:42398543 G>A maps to NM_199002.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:42398543 G>A maps to NM_199002.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:48945046 C>T maps to NM_000836.2 Y758Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:48945046 C>T maps to NM_000836.2 Y758Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:52249296 G>A maps to NM_002029.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr19:52249296 G>A maps to NM_002029.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:85836145 C>T maps to NM_001013649.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:85836145 C>T maps to NM_001013649.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:201337624 C>T maps to ENST00000409151 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:201337624 C>T maps to ENST00000409151 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:234851382 C>T maps to NM_024080.4 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:234851382 C>T maps to NM_024080.4 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:241728661 C>T maps to ENST00000373308 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr2:241728661 C>T maps to ENST00000373308 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr20:62126253 G>A maps to NM_001958.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr20:62126253 G>A maps to NM_001958.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr21:45657074 C>T maps to ENST00000400379 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr21:45657074 C>T maps to ENST00000400379 A27A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-5858-01A-01D-1696-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-06-5858-01A-01D-1696-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr22:26906085 G>A maps to NM_012143.2 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr22:26906085 G>A maps to NM_012143.2 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:69097036 C>T maps to NM_007114.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:69097036 C>T maps to NM_007114.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:124017687 G>A maps to NM_001024660.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:124017687 G>A maps to NM_001024660.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:184298248 C>T maps to NM_004443.3 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:184298248 C>T maps to NM_004443.3 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:185245281 G>A maps to NM_139248.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr3:185245281 G>A maps to NM_139248.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr4:159567946 C>T maps to ENST00000440678 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr4:159567946 C>T maps to ENST00000440678 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr4:177143568 A>G maps to NM_080874.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr4:177143568 A>G maps to NM_080874.3 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:66416868 C>T maps to NM_001164664.1 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:66416868 C>T maps to NM_001164664.1 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:113740526 C>T maps to NM_021614.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:113740526 C>T maps to NM_021614.2 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:140502470 G>A maps to NM_018938.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:140502470 G>A maps to NM_018938.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:140789385 G>A maps to NM_018926.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:140789385 G>A maps to NM_018926.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:149497260 G>A maps to NM_002609.3 N1019N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:149497260 G>A maps to NM_002609.3 N1019N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:176078840 G>A maps to NM_012171.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr5:176078840 G>A maps to NM_012171.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:2770517 C>T maps to NM_020135.2 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:2770517 C>T maps to NM_020135.2 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:32008214 C>T maps to NM_000500.5 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:32008214 C>T maps to NM_000500.5 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:46836809 C>T maps to NM_015234.4 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:46836809 C>T maps to NM_015234.4 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:149699410 A>G maps to NM_015093.4 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr6:149699410 A>G maps to NM_015093.4 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:4900643 C>T maps to NM_020144.4 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:4900643 C>T maps to NM_020144.4 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:5521488 G>T maps to NM_024963.4 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:5521488 G>T maps to NM_024963.4 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:5540354 G>A maps to ENST00000312577 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:5540354 G>A maps to ENST00000312577 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:44806135 G>A maps to NM_031449.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:44806135 G>A maps to NM_031449.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:47342938 G>A maps to NM_022748.11 F1022F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:47342938 G>A maps to NM_022748.11 F1022F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:64168850 A>G maps to NM_016220.3 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:64168850 A>G maps to NM_016220.3 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:75511204 C>T maps to NM_001040456.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:75511204 C>T maps to NM_001040456.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:103014905 C>A maps to ENST00000354356 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:103014905 C>A maps to ENST00000354356 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:103162531 G>A maps to ENST00000428762 N2535N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:103162531 G>A maps to ENST00000428762 N2535N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:121773678 G>A maps to NM_005763.3 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:121773678 G>A maps to NM_005763.3 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:129357144 G>A maps to ENST00000393231 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:129357144 G>A maps to ENST00000393231 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:130021607 G>A maps to NM_001868.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:130021607 G>A maps to NM_001868.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:148815401 C>T maps to NM_001001661.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:148815401 C>T maps to NM_001001661.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:157370775 G>A maps to NM_002847.3 N851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr7:157370775 G>A maps to NM_002847.3 N851N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr8:144732158 G>A maps to NM_014789.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr8:144732158 G>A maps to NM_014789.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:116994127 C>T maps to NM_032888.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:116994127 C>T maps to NM_032888.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:124528841 G>A maps to ENST00000408936 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:124528841 G>A maps to ENST00000408936 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:135073843 G>A maps to NM_032536.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:135073843 G>A maps to NM_032536.2 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:139350206 C>T maps to NM_014866.1 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:139350206 C>T maps to NM_014866.1 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:140128880 G>A maps to NM_080877.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chr9:140128880 G>A maps to NM_080877.2 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chrX:35993897 C>T maps to NM_152632.3 R861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chrX:35993897 C>T maps to NM_152632.3 R861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chrX:153587695 G>A maps to NM_001110556.1 D1407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5858-01A-01D-1696-08 chrX:153587695 G>A maps to NM_001110556.1 D1407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr1:22902984 C>T maps to NM_020526.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr1:22902984 C>T maps to NM_020526.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr14:24108198 G>A maps to NM_182908.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr14:24108198 G>A maps to NM_182908.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr15:90168463 C>T maps to NM_152259.3 T1641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr15:90168463 C>T maps to NM_152259.3 T1641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr16:30721205 G>A maps to NM_006662.2 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr16:30721205 G>A maps to NM_006662.2 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr19:39219649 C>T maps to NM_004924.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr19:39219649 C>T maps to NM_004924.3 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr19:40396028 C>T maps to NM_003890.2 S2456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr19:40396028 C>T maps to NM_003890.2 S2456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr2:56599612 G>A maps to NM_001080433.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr2:56599612 G>A maps to NM_001080433.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr3:9594192 G>T maps to NM_198560.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr3:9594192 G>T maps to NM_198560.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr3:50386327 G>A maps to NM_006545.4 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr3:50386327 G>A maps to NM_006545.4 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr3:183226007 G>A maps to NM_130446.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr3:183226007 G>A maps to NM_130446.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr5:13762881 C>T maps to NM_001369.2 T3410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr5:13762881 C>T maps to NM_001369.2 T3410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr5:68805300 C>T maps to NM_002538.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr5:68805300 C>T maps to NM_002538.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr7:35712864 C>T maps to NM_022373.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr7:35712864 C>T maps to NM_022373.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr7:129104579 G>A did not map to a codon.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr7:129104579 G>A did not map to a codon.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr7:137686379 G>A maps to NM_194071.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chr7:137686379 G>A maps to NM_194071.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chrX:1584485 G>A maps to NM_178129.4 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5859-01A-01D-1696-08 chrX:1584485 G>A maps to NM_178129.4 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:12172030 C>T maps to NM_001243.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:12172030 C>T maps to NM_001243.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:40131872 G>A maps to NM_032526.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:40131872 G>A maps to NM_032526.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:76272801 T>C maps to NM_002440.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:76272801 T>C maps to NM_002440.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:152857173 G>A maps to NM_030663.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:152857173 G>A maps to NM_030663.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:215799137 T>C maps to ENST00000366943 T5222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr1:215799137 T>C maps to ENST00000366943 T5222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr10:105928528 C>T maps to ENST00000389588 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr10:105928528 C>T maps to ENST00000389588 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr10:115804335 C>T maps to NM_000684.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr10:115804335 C>T maps to NM_000684.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr15:75042327 G>A maps to NM_000761.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr15:75042327 G>A maps to NM_000761.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr16:27374338 C>T maps to NM_000418.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr16:27374338 C>T maps to NM_000418.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr18:5395092 C>A maps to NM_012307.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr18:5395092 C>A maps to NM_012307.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:9091523 G>A maps to NM_024690.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:9091523 G>A maps to NM_024690.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:43576026 C>T maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:43576026 C>T maps to NM_031246.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:43708377 C>T maps to NM_002780.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:43708377 C>T maps to NM_002780.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:56370206 T>A maps to NM_134444.4 L483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr19:56370206 T>A maps to NM_134444.4 L483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr2:17692094 G>A maps to NM_001099218.2 Y1152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr2:17692094 G>A maps to NM_001099218.2 Y1152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr3:154832944 G>A did not map to a codon.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr3:154832944 G>A did not map to a codon.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr4:74735287 G>T did not map to a codon.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr4:74735287 G>T did not map to a codon.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr4:75174231 A>T did not map to a codon.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr4:75174231 A>T did not map to a codon.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr4:96761393 C>T maps to NM_005390.4 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr4:96761393 C>T maps to NM_005390.4 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr5:150925629 G>A maps to NM_001447.2 S1686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr5:150925629 G>A maps to NM_001447.2 S1686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr6:168443352 G>A maps to NM_030615.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr6:168443352 G>A maps to NM_030615.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr7:81386512 G>A maps to NM_000601.4 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr7:81386512 G>A maps to NM_000601.4 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr8:119452170 C>G maps to NM_207506.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chr8:119452170 C>G maps to NM_207506.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chrX:10106936 C>T maps to NM_015691.3 D1015D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chrX:10106936 C>T maps to NM_015691.3 D1015D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chrX:54841850 C>T maps to NM_201222.1 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chrX:54841850 C>T maps to NM_201222.1 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chrX:123205084 T>A maps to NM_001042750.1 Y815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6388-01A-12D-1845-08 chrX:123205084 T>A maps to NM_001042750.1 Y815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr1:183177130 C>T maps to NM_005562.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr1:183177130 C>T maps to NM_005562.2 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr1:247655037 G>A maps to NM_001004698.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr1:247655037 G>A maps to NM_001004698.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr1:248202129 C>G maps to NM_001004686.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr1:248202129 C>G maps to NM_001004686.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr10:73544850 T>C maps to ENST00000398860 N1907N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr10:73544850 T>C maps to ENST00000398860 N1907N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr12:21968798 T>G maps to NM_005691.2 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr12:21968798 T>G maps to NM_005691.2 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr16:21080789 C>T maps to NM_017539.1 E1109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr16:21080789 C>T maps to NM_017539.1 E1109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr16:70977831 G>A maps to NM_032821.2 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr16:70977831 G>A maps to NM_032821.2 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr17:8700983 G>A maps to NM_152599.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr17:8700983 G>A maps to NM_152599.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr2:97007485 G>A maps to NM_015341.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr2:97007485 G>A maps to NM_015341.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr2:121107074 C>T maps to NM_002193.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr2:121107074 C>T maps to NM_002193.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr21:19169181 T>C maps to NM_001100420.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr21:19169181 T>C maps to NM_001100420.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr5:148754110 G>A maps to NM_014443.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr5:148754110 G>A maps to NM_014443.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr6:31847947 A>T maps to ENST00000395728 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr6:31847947 A>T maps to ENST00000395728 I1239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr9:112963590 C>T maps to NM_001012993.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chr9:112963590 C>T maps to NM_001012993.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chrX:71843108 A>G maps to ENST00000373539 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chrX:71843108 A>G maps to ENST00000373539 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chrX:78216343 C>T maps to NM_198333.1 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6389-01A-11D-1696-08 chrX:78216343 C>T maps to NM_198333.1 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr1:247024396 G>A maps to ENST00000428671 I1350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr1:247024396 G>A maps to ENST00000428671 I1350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr13:24871772 C>T maps to ENST00000424834 D1198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr13:24871772 C>T maps to ENST00000424834 D1198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr13:29287612 T>A maps to NM_001135919.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr13:29287612 T>A maps to NM_001135919.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr17:6978468 G>A maps to NM_182906.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr17:6978468 G>A maps to NM_182906.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr17:18058719 G>A maps to ENST00000205890 G2811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr17:18058719 G>A maps to ENST00000205890 G2811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr19:629656 G>A maps to NM_005035.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr19:629656 G>A maps to NM_005035.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr19:35786609 G>A maps to NM_002361.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr19:35786609 G>A maps to NM_002361.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr2:179596191 G>A maps to NM_133378.4 S4523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr2:179596191 G>A maps to NM_133378.4 S4523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr3:49847049 C>T maps to NM_003335.2 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr3:49847049 C>T maps to NM_003335.2 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr3:183677611 T>C maps to NM_005688.2 K797K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr3:183677611 T>C maps to NM_005688.2 K797K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr4:82063965 C>A maps to NM_006259.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr4:82063965 C>A maps to NM_006259.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr4:187630081 G>T maps to ENST00000260147 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr4:187630081 G>T maps to ENST00000260147 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr6:37446253 G>A maps to NM_015050.2 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr6:37446253 G>A maps to NM_015050.2 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr7:45930222 C>T maps to NM_000596.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr7:45930222 C>T maps to NM_000596.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr8:93017372 G>A maps to NM_175634.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr8:93017372 G>A maps to NM_175634.2 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr8:142186754 G>A maps to NM_014957.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr8:142186754 G>A maps to NM_014957.2 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr9:105767005 T>C maps to NM_001340.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6390-01A-11D-1696-08 chr9:105767005 T>C maps to NM_001340.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr1:90400303 C>G maps to NM_001134479.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr1:90400303 C>G maps to NM_001134479.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr1:156264000 T>A maps to NM_144580.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr1:156264000 T>A maps to NM_144580.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr1:156841493 G>A maps to NM_002529.3 W266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr1:156841493 G>A maps to NM_002529.3 W266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr12:14840977 G>A maps to NM_004963.3 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr12:14840977 G>A maps to NM_004963.3 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr12:81110964 G>A maps to NM_005593.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr12:81110964 G>A maps to NM_005593.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr13:109859182 G>A maps to NM_015011.1 *1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr13:109859182 G>A maps to NM_015011.1 *1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr14:21623218 G>A maps to NM_001004731.1 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr14:21623218 G>A maps to NM_001004731.1 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr16:18830976 C>T did not map to a codon.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr16:18830976 C>T did not map to a codon.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr16:21123035 G>A maps to NM_017539.1 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr16:21123035 G>A maps to NM_017539.1 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr19:16664591 G>A maps to NM_024881.4 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr19:16664591 G>A maps to NM_024881.4 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr19:41515192 C>T maps to NM_000767.4 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr19:41515192 C>T maps to NM_000767.4 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr2:152476015 G>A maps to NM_001164507.1 P3607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr2:152476015 G>A maps to NM_001164507.1 P3607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr2:237103655 G>A maps to NM_212556.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr2:237103655 G>A maps to NM_212556.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr20:55021056 G>A maps to NM_020356.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr20:55021056 G>A maps to NM_020356.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr3:38743392 G>A maps to NM_006514.2 Q1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr3:38743392 G>A maps to NM_006514.2 Q1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr3:52469855 C>T maps to NM_020163.1 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr3:52469855 C>T maps to NM_020163.1 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr4:48106928 A>G maps to NM_003328.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr4:48106928 A>G maps to NM_003328.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr5:41051144 T>C maps to ENST00000296803 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr5:41051144 T>C maps to ENST00000296803 E426E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr6:28056506 A>G maps to NM_003447.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr6:28056506 A>G maps to NM_003447.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr7:40899924 G>C maps to NM_001193311.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr7:40899924 G>C maps to NM_001193311.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr7:148506236 A>T maps to NM_004456.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr7:148506236 A>T maps to NM_004456.3 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr8:77766548 G>A maps to NM_024721.4 S2464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr8:77766548 G>A maps to NM_024721.4 S2464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr9:130965823 G>A maps to ENST00000372923 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chr9:130965823 G>A maps to ENST00000372923 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chrX:22051085 A>T did not map to a codon.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chrX:22051085 A>T did not map to a codon.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chrX:27998446 G>C maps to NM_001017930.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chrX:27998446 G>C maps to NM_001017930.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chrX:76938529 C>A maps to NM_000489.3 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6391-01A-11D-1696-08 chrX:76938529 C>A maps to NM_000489.3 E740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr1:985840 C>T maps to NM_198576.2 R1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr1:985840 C>T maps to NM_198576.2 R1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr10:135142373 C>T maps to NM_015722.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr10:135142373 C>T maps to NM_015722.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:3688570 G>A maps to NM_020402.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:3688570 G>A maps to NM_020402.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:55579781 C>T maps to NM_001004738.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:55579781 C>T maps to NM_001004738.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:101818771 A>G maps to NM_020802.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:101818771 A>G maps to NM_020802.2 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:123676993 G>A maps to NM_001005325.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr11:123676993 G>A maps to NM_001005325.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr12:80191151 T>C maps to NM_001143885.1 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr12:80191151 T>C maps to NM_001143885.1 Q705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr12:123187005 C>T maps to NM_177551.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr12:123187005 C>T maps to NM_177551.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr14:38724092 T>A maps to NM_175060.1 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr14:38724092 T>A maps to NM_175060.1 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr14:38724648 G>A maps to NM_175060.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr14:38724648 G>A maps to NM_175060.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr14:51227077 C>G did not map to a codon.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr14:51227077 C>G did not map to a codon.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr15:62300906 C>T maps to NM_020821.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr15:62300906 C>T maps to NM_020821.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr16:57016106 C>T maps to NM_000078.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr16:57016106 C>T maps to NM_000078.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr16:88891240 C>T maps to NM_000512.4 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr16:88891240 C>T maps to NM_000512.4 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr20:62367144 G>A maps to NM_032527.4 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr20:62367144 G>A maps to NM_032527.4 A490A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-06-6693-01A-11D-1845-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-06-6693-01A-11D-1845-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-06-6693-01A-11D-1845-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-06-6693-01A-11D-1845-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr3:93646099 C>T maps to NM_000313.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr3:93646099 C>T maps to NM_000313.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr4:36085015 C>T maps to NM_015230.2 V1494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr4:36085015 C>T maps to NM_015230.2 V1494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr4:79204018 C>T maps to NM_025074.6 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr4:79204018 C>T maps to NM_025074.6 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr7:20180648 C>A maps to NM_182762.3 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr7:20180648 C>A maps to NM_182762.3 E827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr7:55221762 C>G maps to NM_005228.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr7:55221762 C>G maps to NM_005228.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr9:114145510 C>T maps to NM_001080398.1 V1439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chr9:114145510 C>T maps to NM_001080398.1 V1439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chrX:22132589 C>G maps to NM_000444.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chrX:22132589 C>G maps to NM_000444.4 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chrX:27999307 G>A maps to NM_001017930.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6693-01A-11D-1845-08 chrX:27999307 G>A maps to NM_001017930.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:12172042 C>T maps to NM_001243.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:12172042 C>T maps to NM_001243.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:13183577 G>A maps to NM_001136561.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:13183577 G>A maps to NM_001136561.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:59248391 G>A maps to NM_002228.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:59248391 G>A maps to NM_002228.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:150730363 G>A maps to NM_004079.4 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:150730363 G>A maps to NM_004079.4 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:200823984 C>T maps to ENST00000236925 N1299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr1:200823984 C>T maps to ENST00000236925 N1299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr10:95134678 G>A maps to NM_013451.3 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr10:95134678 G>A maps to NM_013451.3 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr10:134165158 G>A maps to NM_030626.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr10:134165158 G>A maps to NM_030626.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:6239210 G>A maps to NM_032127.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:6239210 G>A maps to NM_032127.3 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:68191120 G>A maps to NM_002335.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:68191120 G>A maps to NM_002335.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:72005107 G>A maps to NM_030813.3 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:72005107 G>A maps to NM_030813.3 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:118403821 C>T maps to NM_032780.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr11:118403821 C>T maps to NM_032780.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr12:101880530 A>G maps to ENST00000299272 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr12:101880530 A>G maps to ENST00000299272 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr12:120148179 C>T maps to ENST00000392521 V1649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr12:120148179 C>T maps to ENST00000392521 V1649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr12:130927080 G>A maps to NM_015347.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr12:130927080 G>A maps to NM_015347.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr13:25671128 C>T maps to NM_030979.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr13:25671128 C>T maps to NM_030979.2 R265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr14:20249074 G>T maps to NM_001005500.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr14:20249074 G>T maps to NM_001005500.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr14:24040214 C>T maps to NM_032452.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr14:24040214 C>T maps to NM_032452.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr14:65520031 G>A maps to ENST00000448390 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr14:65520031 G>A maps to ENST00000448390 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr15:52404683 C>T maps to NM_020396.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr15:52404683 C>T maps to NM_020396.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr15:75248657 C>A maps to NM_017793.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr15:75248657 C>A maps to NM_017793.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr15:99251217 C>T maps to NM_000875.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr15:99251217 C>T maps to NM_000875.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr16:31286943 C>T maps to NM_001145808.1 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr16:31286943 C>T maps to NM_001145808.1 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr17:7154553 C>T maps to NM_015343.4 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr17:7154553 C>T maps to NM_015343.4 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr17:49270164 T>C maps to ENST00000389496 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr17:49270164 T>C maps to ENST00000389496 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:22270777 G>A did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:22270777 G>A did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:35175736 C>G maps to ENST00000221282 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:35175736 C>G maps to ENST00000221282 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:49551984 G>A maps to ENST00000448456 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:49551984 G>A maps to ENST00000448456 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:58485725 C>T maps to NM_152474.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr19:58485725 C>T maps to NM_152474.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr2:112944812 G>A maps to NM_153214.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr2:112944812 G>A maps to NM_153214.2 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr2:169814524 C>T maps to NM_003742.2 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr2:169814524 C>T maps to NM_003742.2 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr20:30409481 C>T maps to NM_033118.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr20:30409481 C>T maps to NM_033118.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr20:43115267 T>C maps to NM_024331.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr20:43115267 T>C maps to NM_024331.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr21:47421891 G>A maps to NM_001848.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr21:47421891 G>A maps to NM_001848.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr22:17072054 G>A maps to NM_014406.4 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr22:17072054 G>A maps to NM_014406.4 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr3:9489392 C>T maps to ENST00000407969 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr3:9489392 C>T maps to ENST00000407969 V621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr3:68929926 G>T maps to NM_182522.3 C28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr3:68929926 G>T maps to NM_182522.3 C28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr4:84368059 T>C maps to NM_133636.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr4:84368059 T>C maps to NM_133636.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr4:96075769 G>C maps to ENST00000440890 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr4:96075769 G>C maps to ENST00000440890 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr4:107845337 G>A maps to NM_014421.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr4:107845337 G>A maps to NM_014421.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr5:71015194 C>T maps to NM_004291.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr5:71015194 C>T maps to NM_004291.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr6:70042888 A>G maps to NM_001704.2 K1059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr6:70042888 A>G maps to NM_001704.2 K1059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr6:110959909 C>T did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr6:110959909 C>T did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr6:160998166 C>T did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr6:160998166 C>T did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr7:100490908 G>A maps to NM_000665.3 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr7:100490908 G>A maps to NM_000665.3 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr7:100692246 G>A maps to NM_001040105.1 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr7:100692246 G>A maps to NM_001040105.1 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr8:12952343 C>T maps to NM_182643.2 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr8:12952343 C>T maps to NM_182643.2 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr8:22020639 C>T maps to NM_003018.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr8:22020639 C>T maps to NM_003018.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr9:97063381 C>T maps to NM_194320.2 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chr9:97063381 C>T maps to NM_194320.2 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:17819725 G>A maps to NM_021785.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:17819725 G>A maps to NM_021785.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:53439848 C>T did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:53439848 C>T did not map to a codon.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:78216910 C>T maps to NM_198333.1 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:78216910 C>T maps to NM_198333.1 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:102005059 T>A maps to NM_001142530.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:102005059 T>A maps to NM_001142530.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:153581221 G>A maps to NM_001110556.1 D2099D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6694-01A-12D-1845-08 chrX:153581221 G>A maps to NM_001110556.1 D2099D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr1:16892155 T>C maps to NM_017940.3 K1013K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr1:16892155 T>C maps to NM_017940.3 K1013K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr1:205897956 G>A maps to NM_134325.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr1:205897956 G>A maps to NM_134325.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr10:1284234 C>T maps to NM_018702.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr10:1284234 C>T maps to NM_018702.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr10:50530622 G>A maps to NM_001135196.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr10:50530622 G>A maps to NM_001135196.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr11:126343281 G>A maps to NM_032531.3 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr11:126343281 G>A maps to NM_032531.3 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr13:110819538 A>C maps to NM_001845.4 G1305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr13:110819538 A>C maps to NM_001845.4 G1305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr14:105409916 G>A maps to NM_138420.2 A3957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr14:105409916 G>A maps to NM_138420.2 A3957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr16:81953270 T>A did not map to a codon.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr16:81953270 T>A did not map to a codon.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr16:89347129 G>A maps to NM_013275.4 S1940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr16:89347129 G>A maps to NM_013275.4 S1940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr19:12813635 C>T did not map to a codon.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr19:12813635 C>T did not map to a codon.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr19:55327960 G>A maps to ENST00000355608 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr19:55327960 G>A maps to ENST00000355608 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr20:30674578 C>T maps to NM_002110.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr20:30674578 C>T maps to NM_002110.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr20:31829274 C>T maps to NM_130852.2 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr20:31829274 C>T maps to NM_130852.2 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr3:38645337 G>A maps to NM_001099404.1 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr3:38645337 G>A maps to NM_001099404.1 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr4:3534103 C>G maps to NM_002337.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr4:3534103 C>G maps to NM_002337.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr5:138658285 G>A did not map to a codon.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr5:138658285 G>A did not map to a codon.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr6:51900448 C>T maps to NM_138694.3 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr6:51900448 C>T maps to NM_138694.3 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr6:106999810 A>T maps to NM_001624.2 G1391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr6:106999810 A>T maps to NM_001624.2 G1391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr7:44046878 T>C maps to NM_175064.2 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr7:44046878 T>C maps to NM_175064.2 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr9:90536102 C>T maps to NM_001145124.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6695-01A-11D-1845-08 chr9:90536102 C>T maps to NM_001145124.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr1:12919079 G>A maps to NM_023014.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr1:12919079 G>A maps to NM_023014.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr1:23720437 G>A maps to NM_003196.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr1:23720437 G>A maps to NM_003196.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr1:57480757 C>T maps to ENST00000371231 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr1:57480757 C>T maps to ENST00000371231 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr11:57982887 T>C maps to NM_001004458.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr11:57982887 T>C maps to NM_001004458.1 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr12:10587962 G>T maps to NM_002260.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr12:10587962 G>T maps to NM_002260.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr12:48181753 G>A did not map to a codon.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr12:48181753 G>A did not map to a codon.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr12:85459185 T>C maps to NM_001079910.1 D846D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr12:85459185 T>C maps to NM_001079910.1 D846D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr17:26094857 G>A maps to NM_000625.4 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr17:26094857 G>A maps to NM_000625.4 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr17:33904177 G>A maps to NM_000286.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr17:33904177 G>A maps to NM_000286.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr17:56699011 C>A maps to ENST00000240361 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr17:56699011 C>A maps to ENST00000240361 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr19:54823843 G>A maps to NM_021250.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr19:54823843 G>A maps to NM_021250.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr2:46609717 G>A maps to NM_001430.4 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr2:46609717 G>A maps to NM_001430.4 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr2:169939875 C>T maps to NM_001142271.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr2:169939875 C>T maps to NM_001142271.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr2:179599470 G>A maps to NM_133378.4 V3816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr2:179599470 G>A maps to NM_133378.4 V3816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr21:46021294 A>C maps to ENST00000380102 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr21:46021294 A>C maps to ENST00000380102 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr5:37183581 A>C maps to NM_023073.3 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr5:37183581 A>C maps to NM_023073.3 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr7:4050625 C>T maps to NM_152744.3 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr7:4050625 C>T maps to NM_152744.3 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr7:82784327 C>T maps to NM_033026.5 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr7:82784327 C>T maps to NM_033026.5 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr8:71057068 G>A maps to NM_006540.2 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr8:71057068 G>A maps to NM_006540.2 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr9:91973080 G>A maps to NM_024077.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6697-01A-11D-1845-08 chr9:91973080 G>A maps to NM_024077.3 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr1:1392508 C>T maps to NM_001039211.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr1:1392508 C>T maps to NM_001039211.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr11:4790373 C>T maps to ENST00000380383 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr11:4790373 C>T maps to ENST00000380383 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr11:119052982 C>T maps to NM_024618.2 N845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr11:119052982 C>T maps to NM_024618.2 N845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr12:49726938 G>A maps to NM_001008223.1 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr12:49726938 G>A maps to NM_001008223.1 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr13:39613425 G>A did not map to a codon.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr13:39613425 G>A did not map to a codon.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr13:48916733 G>A did not map to a codon.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr13:48916733 G>A did not map to a codon.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr17:29661897 G>A maps to NM_001042492.2 W1952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr17:29661897 G>A maps to NM_001042492.2 W1952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr17:56344836 C>T maps to NM_006151.2 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr17:56344836 C>T maps to NM_006151.2 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr18:77624158 C>T maps to NM_012283.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr18:77624158 C>T maps to NM_012283.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr19:46733407 C>T maps to NM_198541.1 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr19:46733407 C>T maps to NM_198541.1 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr2:217285032 C>T maps to NM_014140.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr2:217285032 C>T maps to NM_014140.3 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr20:51870293 C>T maps to NM_173485.5 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr20:51870293 C>T maps to NM_173485.5 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr5:39202819 C>T maps to ENST00000263405 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr5:39202819 C>T maps to ENST00000263405 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr9:86571235 G>A maps to NM_032307.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chr9:86571235 G>A maps to NM_032307.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chrX:77109425 T>C maps to NM_032121.5 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6698-01A-11D-1845-08 chrX:77109425 T>C maps to NM_032121.5 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr1:236343285 C>T maps to NM_003272.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr1:236343285 C>T maps to NM_003272.3 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr12:56733734 T>C maps to NM_016584.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr12:56733734 T>C maps to NM_016584.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr13:51825703 C>T maps to NM_145019.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr13:51825703 C>T maps to NM_145019.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr15:24921106 C>T maps to NM_018958.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr15:24921106 C>T maps to NM_018958.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr16:1129344 G>A maps to NM_001053.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr16:1129344 G>A maps to NM_001053.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr17:18891568 C>T maps to NM_001039999.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr17:18891568 C>T maps to NM_001039999.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr18:14803788 A>G maps to NM_001145029.1 Q750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr18:14803788 A>G maps to NM_001145029.1 Q750Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr19:41083169 C>A maps to NM_138392.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr19:41083169 C>A maps to NM_138392.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr19:56047475 G>A maps to NM_001101401.2 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr19:56047475 G>A maps to NM_001101401.2 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr20:61959710 C>T maps to ENST00000326996 H1259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr20:61959710 C>T maps to ENST00000326996 H1259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr4:155157532 G>A maps to NM_017639.3 V2302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr4:155157532 G>A maps to NM_017639.3 V2302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr5:162949 C>T maps to NM_052909.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr5:162949 C>T maps to NM_052909.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr5:140188685 C>T maps to NM_018907.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr5:140188685 C>T maps to NM_018907.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr7:73010590 C>A maps to NM_032951.2 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr7:73010590 C>A maps to NM_032951.2 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr7:103032067 C>T did not map to a codon.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr7:103032067 C>T did not map to a codon.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr8:10396128 C>T maps to NM_198464.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chr8:10396128 C>T maps to NM_198464.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chrX:18622186 C>A maps to NM_001037343.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chrX:18622186 C>A maps to NM_001037343.1 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chrX:49048187 G>A maps to NM_003179.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chrX:49048187 G>A maps to NM_003179.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chrX:69825266 G>T maps to NM_001003811.1 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6699-01A-11D-1845-08 chrX:69825266 G>T maps to NM_001003811.1 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr1:247712511 C>T maps to NM_145278.3 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr1:247712511 C>T maps to NM_145278.3 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr11:59211009 C>T maps to NM_001004728.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr11:59211009 C>T maps to NM_001004728.1 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr11:59564775 G>T maps to NM_004177.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr11:59564775 G>T maps to NM_004177.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr12:8813464 G>A maps to NM_003480.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr12:8813464 G>A maps to NM_003480.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr14:94103592 C>T maps to ENST00000393153 N1977N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr14:94103592 C>T maps to ENST00000393153 N1977N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr15:101971635 C>T maps to NM_002570.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr15:101971635 C>T maps to NM_002570.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr16:70172799 A>G did not map to a codon.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr16:70172799 A>G did not map to a codon.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr17:8784973 G>A maps to NM_001142633.1 N785N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr17:8784973 G>A maps to NM_001142633.1 N785N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr18:30825370 G>A maps to NM_001105528.1 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr18:30825370 G>A maps to NM_001105528.1 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr18:61306945 G>A maps to NM_002974.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr18:61306945 G>A maps to NM_002974.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr19:41630792 C>T maps to NM_000774.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr19:41630792 C>T maps to NM_000774.3 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr2:96906136 C>T maps to NM_001037228.1 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr2:96906136 C>T maps to NM_001037228.1 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr2:125530373 A>T did not map to a codon.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr2:125530373 A>T did not map to a codon.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr2:130948159 G>A maps to ENST00000409255 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr2:130948159 G>A maps to ENST00000409255 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr3:16343239 A>G maps to NM_138381.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr3:16343239 A>G maps to NM_138381.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr3:51430155 G>A maps to NM_013286.4 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr3:51430155 G>A maps to NM_013286.4 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr5:10394248 G>A maps to NM_005885.2 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr5:10394248 G>A maps to NM_005885.2 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr6:55264167 A>T maps to NM_207410.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr6:55264167 A>T maps to NM_207410.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr7:82595086 T>C maps to NM_033026.5 T1339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr7:82595086 T>C maps to NM_033026.5 T1339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr7:134222352 C>G maps to NM_020299.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chr7:134222352 C>G maps to NM_020299.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chrX:31089935 G>A maps to NM_031894.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6700-01A-12D-1845-08 chrX:31089935 G>A maps to NM_031894.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr1:38197143 C>T maps to NM_001099439.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr1:38197143 C>T maps to NM_001099439.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr10:97607462 G>A maps to NM_001098175.1 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr10:97607462 G>A maps to NM_001098175.1 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr10:124813242 T>C maps to NM_001609.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr10:124813242 T>C maps to NM_001609.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr11:5012727 T>C did not map to a codon.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr11:5012727 T>C did not map to a codon.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr12:49391284 C>T maps to NM_015086.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr12:49391284 C>T maps to NM_015086.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr13:38320376 G>A maps to NM_003306.1 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr13:38320376 G>A maps to NM_003306.1 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr15:90610833 C>T maps to NM_198526.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr15:90610833 C>T maps to NM_198526.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr17:26851528 C>T maps to NM_003593.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr17:26851528 C>T maps to NM_003593.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr17:27939700 G>A maps to NM_152345.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr17:27939700 G>A maps to NM_152345.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr19:15734859 G>A maps to NM_007253.3 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr19:15734859 G>A maps to NM_007253.3 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr19:43420414 G>A maps to NM_002782.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr19:43420414 G>A maps to NM_002782.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr19:49867854 C>T maps to NM_014419.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr19:49867854 C>T maps to NM_014419.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr2:180634431 G>A maps to NM_152520.4 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr2:180634431 G>A maps to NM_152520.4 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr2:227661258 G>C maps to NM_005544.2 Y732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr2:227661258 G>C maps to NM_005544.2 Y732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr4:79429982 C>A maps to NM_025074.6 P3201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr4:79429982 C>A maps to NM_025074.6 P3201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr9:139934425 G>C maps to ENST00000371600 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-6701-01A-11D-1845-08 chr9:139934425 G>C maps to ENST00000371600 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr1:47838724 C>T maps to NM_016308.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr1:47838724 C>T maps to NM_016308.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr1:248512861 G>A maps to NM_001001918.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr1:248512861 G>A maps to NM_001001918.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr11:45891982 G>A maps to NM_021117.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr11:45891982 G>A maps to NM_021117.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr19:39205182 C>T maps to NM_004924.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr19:39205182 C>T maps to NM_004924.3 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr19:49132915 C>T maps to NM_020126.3 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr19:49132915 C>T maps to NM_020126.3 G617G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr6:33380058 C>T maps to NM_024165.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-08-0386-01A-01D-1492-08 chr6:33380058 C>T maps to NM_024165.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr1:152060547 G>A maps to NM_001008536.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr1:152060547 G>A maps to NM_001008536.1 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr11:72423532 G>A maps to NM_001040118.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr11:72423532 G>A maps to NM_001040118.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr12:93968660 C>T maps to NM_003877.3 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr12:93968660 C>T maps to NM_003877.3 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr17:61613121 G>A maps to NM_030779.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr17:61613121 G>A maps to NM_030779.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr19:1250465 C>G maps to NM_177401.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr19:1250465 C>G maps to NM_177401.4 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr19:10444147 C>T maps to NM_133452.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr19:10444147 C>T maps to NM_133452.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr2:167262323 T>C maps to NM_002976.2 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr2:167262323 T>C maps to NM_002976.2 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr2:219131280 G>A maps to ENST00000444053 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr2:219131280 G>A maps to ENST00000444053 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr20:17389924 C>T maps to NM_002594.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr20:17389924 C>T maps to NM_002594.2 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr21:19775930 C>T maps to NM_002772.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr21:19775930 C>T maps to NM_002772.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr3:68055846 C>T maps to NM_213609.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr3:68055846 C>T maps to NM_213609.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr3:189700929 C>T did not map to a codon.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr3:189700929 C>T did not map to a codon.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr4:154702674 C>T maps to NM_003013.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr4:154702674 C>T maps to NM_003013.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr5:82815366 T>C maps to NM_004385.4 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr5:82815366 T>C maps to NM_004385.4 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr6:34935027 G>A maps to NM_015245.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr6:34935027 G>A maps to NM_015245.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr6:39033980 G>A maps to NM_002062.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr6:39033980 G>A maps to NM_002062.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr6:125379095 C>T maps to NM_152553.2 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr6:125379095 C>T maps to NM_152553.2 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr7:138447095 G>A maps to NM_130840.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr7:138447095 G>A maps to NM_130840.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr8:8239065 A>G maps to NM_001080826.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr8:8239065 A>G maps to NM_001080826.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr8:67546806 C>A maps to NM_025054.4 E1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr8:67546806 C>A maps to NM_025054.4 E1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr9:100823173 C>T maps to NM_018946.3 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr9:100823173 C>T maps to NM_018946.3 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr9:113173810 G>T maps to ENST00000374463 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chr9:113173810 G>T maps to ENST00000374463 L2063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chrX:10066543 A>T did not map to a codon.
Sequencing variant TCGA-12-0615-01A-01D-1492-08 chrX:10066543 A>T did not map to a codon.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr1:167806485 C>T did not map to a codon.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr1:167806485 C>T did not map to a codon.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr1:226040424 G>A maps to NM_014698.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr1:226040424 G>A maps to NM_014698.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr14:34270128 C>T maps to NM_001164749.1 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr14:34270128 C>T maps to NM_001164749.1 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr17:42882693 G>A maps to NM_001080383.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr17:42882693 G>A maps to NM_001080383.1 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr17:48072314 G>A maps to NM_005220.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr17:48072314 G>A maps to NM_005220.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr19:44934109 C>T maps to NM_014518.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr19:44934109 C>T maps to NM_014518.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr2:152477435 A>G maps to NM_001164507.1 S3519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr2:152477435 A>G maps to NM_001164507.1 S3519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr22:46793604 G>A maps to NM_014246.1 D1889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr22:46793604 G>A maps to NM_014246.1 D1889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr3:121980781 C>T maps to NM_001178065.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr3:121980781 C>T maps to NM_001178065.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr4:55592079 G>A maps to NM_000222.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr4:55592079 G>A maps to NM_000222.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr5:180582406 C>T maps to NM_206880.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr5:180582406 C>T maps to NM_206880.1 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr7:77552025 G>A maps to ENST00000427986 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr7:77552025 G>A maps to ENST00000427986 V350V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr9:85958186 A>G maps to NM_174938.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr9:85958186 A>G maps to NM_174938.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr9:136230530 G>A maps to NM_033161.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chr9:136230530 G>A maps to NM_033161.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chrX:140995244 G>A maps to NM_005462.4 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0616-01A-01D-1492-08 chrX:140995244 G>A maps to NM_005462.4 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr1:158585036 G>A maps to NM_003126.2 Q2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr1:158585036 G>A maps to NM_003126.2 Q2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr1:173155864 G>A maps to NM_003326.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr1:173155864 G>A maps to NM_003326.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr1:226420895 T>C did not map to a codon.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr1:226420895 T>C did not map to a codon.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr11:61898062 G>A did not map to a codon.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr11:61898062 G>A did not map to a codon.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr12:69229606 A>G did not map to a codon.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr12:69229606 A>G did not map to a codon.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr18:60243793 G>A maps to NM_017742.4 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr18:60243793 G>A maps to NM_017742.4 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr19:49398650 G>A maps to NM_003323.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr19:49398650 G>A maps to NM_003323.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr2:12858628 T>C maps to NM_021643.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr2:12858628 T>C maps to NM_021643.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr2:233899563 C>T maps to NM_005383.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr2:233899563 C>T maps to NM_005383.2 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr2:238280768 G>A maps to NM_004369.3 N1297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr2:238280768 G>A maps to NM_004369.3 N1297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr20:35865067 G>A maps to NM_002951.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr20:35865067 G>A maps to NM_002951.3 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr22:31524556 C>T maps to ENST00000331075 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr22:31524556 C>T maps to ENST00000331075 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr22:42456399 T>G maps to NM_000262.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr22:42456399 T>G maps to NM_000262.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:32975994 G>A maps to NM_002119.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:32975994 G>A maps to NM_002119.3 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:43163922 C>A maps to ENST00000354495 I835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:43163922 C>A maps to ENST00000354495 I835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:49696553 G>A maps to NM_001190986.1 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:49696553 G>A maps to NM_001190986.1 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:157522506 C>T maps to ENST00000367148 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr6:157522506 C>T maps to ENST00000367148 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr8:22069180 A>G maps to NM_006129.4 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0618-01A-01D-1492-08 chr8:22069180 A>G maps to NM_006129.4 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr10:90674394 G>T maps to NM_020799.2 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr10:90674394 G>T maps to NM_020799.2 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr12:7980152 G>A maps to NM_153449.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr12:7980152 G>A maps to NM_153449.2 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr12:8082341 G>A maps to NM_006931.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr12:8082341 G>A maps to NM_006931.2 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr12:113565892 G>C maps to NM_001193520.1 Y71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr12:113565892 G>C maps to NM_001193520.1 Y71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr14:35005431 G>A maps to NM_018453.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr14:35005431 G>A maps to NM_018453.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr16:20492161 G>A maps to NM_001010845.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr16:20492161 G>A maps to NM_001010845.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr16:26147418 G>A maps to NM_006040.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr16:26147418 G>A maps to NM_006040.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr17:48275130 G>A maps to NM_000088.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr17:48275130 G>A maps to NM_000088.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr17:71426662 G>A maps to NM_001144952.1 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr17:71426662 G>A maps to NM_001144952.1 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr19:9067036 A>G maps to NM_024690.2 S6803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr19:9067036 A>G maps to NM_024690.2 S6803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr19:46318326 C>T maps to NM_030785.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr19:46318326 C>T maps to NM_030785.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr20:30672224 G>A maps to NM_002110.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr20:30672224 G>A maps to NM_002110.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr22:20458190 G>A maps to NM_015672.1 G1037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr22:20458190 G>A maps to NM_015672.1 G1037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr3:38755493 G>A maps to NM_006514.2 R1253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr3:38755493 G>A maps to NM_006514.2 R1253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr3:185823618 G>A maps to NM_004454.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr3:185823618 G>A maps to NM_004454.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr4:1725207 C>T maps to NM_006342.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr4:1725207 C>T maps to NM_006342.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr4:158284177 C>T maps to NM_000826.3 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr4:158284177 C>T maps to NM_000826.3 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr5:140236991 G>A maps to NM_018901.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr5:140236991 G>A maps to NM_018901.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr9:131233666 C>T maps to NM_153435.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr9:131233666 C>T maps to NM_153435.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr9:133540123 C>T maps to NM_021619.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0619-01A-01D-1492-08 chr9:133540123 C>T maps to NM_021619.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr1:17699700 G>A maps to NM_207421.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr1:17699700 G>A maps to NM_207421.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr1:152883943 A>C maps to NM_005547.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr1:152883943 A>C maps to NM_005547.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr11:62749351 C>A maps to NM_004790.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr11:62749351 C>A maps to NM_004790.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr12:13061398 C>T maps to NM_003979.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr12:13061398 C>T maps to NM_003979.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr16:67572595 G>A maps to NM_001193523.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr16:67572595 G>A maps to NM_001193523.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr17:30348507 T>C maps to ENST00000327564 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr17:30348507 T>C maps to ENST00000327564 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr18:25591941 A>C maps to NM_001792.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr18:25591941 A>C maps to NM_001792.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:7591684 G>A maps to NM_020533.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:7591684 G>A maps to NM_020533.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:7832493 C>T maps to NM_014257.4 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:7832493 C>T maps to NM_014257.4 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:40380304 G>A maps to NM_003890.2 F3670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:40380304 G>A maps to NM_003890.2 F3670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:40902797 C>T maps to NM_181882.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:40902797 C>T maps to NM_181882.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:53453299 T>C maps to NM_001031665.1 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr19:53453299 T>C maps to NM_001031665.1 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr20:35835809 T>C maps to NM_002951.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr20:35835809 T>C maps to NM_002951.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr20:45194936 G>A maps to NM_022829.5 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr20:45194936 G>A maps to NM_022829.5 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr21:47532418 C>T maps to NM_001849.3 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr21:47532418 C>T maps to NM_001849.3 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr3:128757681 G>A maps to NM_024768.2 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr3:128757681 G>A maps to NM_024768.2 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr3:196388088 C>T maps to NM_198565.1 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr3:196388088 C>T maps to NM_198565.1 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr4:15964314 C>T maps to NM_031950.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr4:15964314 C>T maps to NM_031950.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr4:110908979 T>C maps to NM_001963.4 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr4:110908979 T>C maps to NM_001963.4 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr5:180048602 G>A maps to NM_182925.4 C653C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr5:180048602 G>A maps to NM_182925.4 C653C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr6:35747187 C>A maps to NM_207409.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr6:35747187 C>A maps to NM_207409.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr6:54806090 G>A maps to NM_001010872.1 K774K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr6:54806090 G>A maps to NM_001010872.1 K774K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr7:65554648 C>G maps to NM_000048.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr7:65554648 C>G maps to NM_000048.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr8:52321473 C>A maps to NM_144651.4 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr8:52321473 C>A maps to NM_144651.4 E904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr8:105360770 C>T did not map to a codon.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr8:105360770 C>T did not map to a codon.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr8:144808804 G>A maps to NM_198488.3 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr8:144808804 G>A maps to NM_198488.3 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr9:94486081 C>T maps to NM_004560.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr9:94486081 C>T maps to NM_004560.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr9:140201419 C>T maps to NM_017820.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chr9:140201419 C>T maps to NM_017820.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chrX:137785219 G>A maps to NM_001139500.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0688-01A-02D-1492-08 chrX:137785219 G>A maps to NM_001139500.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr1:10493979 C>T maps to NM_198544.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr1:10493979 C>T maps to NM_198544.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr1:161993079 G>A maps to ENST00000451379 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr1:161993079 G>A maps to ENST00000451379 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr1:183514092 C>T maps to ENST00000367537 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr1:183514092 C>T maps to ENST00000367537 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr10:70496805 G>C did not map to a codon.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr10:70496805 G>C did not map to a codon.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr11:3849146 C>T maps to NM_001665.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr11:3849146 C>T maps to NM_001665.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr11:68315673 T>G did not map to a codon.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr11:68315673 T>G did not map to a codon.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr12:130847605 A>G maps to NM_004764.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr12:130847605 A>G maps to NM_004764.4 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr14:25042968 G>A maps to NM_001911.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr14:25042968 G>A maps to NM_001911.2 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr14:50802890 A>G maps to ENST00000356146 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr14:50802890 A>G maps to ENST00000356146 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr14:94394936 C>T maps to NM_138344.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr14:94394936 C>T maps to NM_138344.3 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr15:34528394 T>C maps to NM_133647.1 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr15:34528394 T>C maps to NM_133647.1 Q1016Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr15:75116022 G>A maps to NM_021819.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr15:75116022 G>A maps to NM_021819.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr16:68288908 G>A maps to NM_012320.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr16:68288908 G>A maps to NM_012320.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr19:56388508 G>A maps to NM_134444.4 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr19:56388508 G>A maps to NM_134444.4 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr2:116593730 A>G did not map to a codon.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr2:116593730 A>G did not map to a codon.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr2:178990755 T>C maps to ENST00000456670 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr2:178990755 T>C maps to ENST00000456670 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr20:40043954 T>C maps to NM_032221.3 G2270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr20:40043954 T>C maps to NM_032221.3 G2270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr20:43995682 C>T maps to NM_033542.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr20:43995682 C>T maps to NM_033542.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr4:189060966 G>A maps to NM_178556.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr4:189060966 G>A maps to NM_178556.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr6:47976382 C>T maps to NM_001013732.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr6:47976382 C>T maps to NM_001013732.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr6:167754815 G>C maps to NM_031949.4 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr6:167754815 G>C maps to NM_031949.4 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr7:23825129 C>T maps to NM_031414.3 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr7:23825129 C>T maps to NM_031414.3 R728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr8:23709002 G>A maps to NM_003155.2 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr8:23709002 G>A maps to NM_003155.2 N101N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr9:116811354 C>T maps to ENST00000374126 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr9:116811354 C>T maps to ENST00000374126 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr9:125748578 G>T maps to NM_012197.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chr9:125748578 G>T maps to NM_012197.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chrX:24759539 C>T maps to ENST00000379068 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chrX:24759539 C>T maps to ENST00000379068 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chrX:153694762 C>T maps to NM_017514.3 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0692-01A-01W-0348-08 chrX:153694762 C>T maps to NM_017514.3 S948S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr1:26515153 G>A maps to ENST00000374253 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr1:26515153 G>A maps to ENST00000374253 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr1:45553631 G>A maps to NM_020883.1 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr1:45553631 G>A maps to NM_020883.1 H291H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr1:160786528 C>G maps to ENST00000263285 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr1:160786528 C>G maps to ENST00000263285 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr10:89550115 G>A maps to NM_032810.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr10:89550115 G>A maps to NM_032810.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr10:103557791 A>C maps to NM_012215.3 Y643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr10:103557791 A>C maps to NM_012215.3 Y643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr11:17757794 G>T maps to NM_001112741.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr11:17757794 G>T maps to NM_001112741.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr11:18554016 A>G maps to NM_001040697.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr11:18554016 A>G maps to NM_001040697.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr11:116691954 G>A maps to NM_000482.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr11:116691954 G>A maps to NM_000482.3 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr12:85450301 T>C maps to NM_001079910.1 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr12:85450301 T>C maps to NM_001079910.1 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr13:29004212 C>T maps to NM_002019.4 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr13:29004212 C>T maps to NM_002019.4 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr14:68247032 C>T maps to NM_015346.3 W1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr14:68247032 C>T maps to NM_015346.3 W1533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr14:94849083 G>T maps to NM_001127707.1 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr14:94849083 G>T maps to NM_001127707.1 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr16:87448974 T>G did not map to a codon.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr16:87448974 T>G did not map to a codon.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr17:4542380 C>G maps to NM_001140.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr17:4542380 C>G maps to NM_001140.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr19:3961152 G>A maps to NM_001348.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr19:3961152 G>A maps to NM_001348.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr19:19638107 C>T maps to ENST00000436926 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr19:19638107 C>T maps to ENST00000436926 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr19:46094671 C>T maps to NM_005282.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr19:46094671 C>T maps to NM_005282.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr2:74592697 G>A maps to NM_004082.4 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr2:74592697 G>A maps to NM_004082.4 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr2:227659845 T>G maps to NM_005544.2 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr2:227659845 T>G maps to NM_005544.2 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr22:29440866 C>T maps to NM_032173.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr22:29440866 C>T maps to NM_032173.2 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr3:46759086 A>C maps to NM_013270.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr3:46759086 A>C maps to NM_013270.4 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr4:13543970 C>G maps to NM_001189.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr4:13543970 C>G maps to NM_001189.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr4:38698728 G>T maps to NM_016531.5 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr4:38698728 G>T maps to NM_016531.5 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr5:140011716 C>T maps to NM_001174105.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr5:140011716 C>T maps to NM_001174105.1 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr5:167880984 G>A maps to NM_001161661.1 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr5:167880984 G>A maps to NM_001161661.1 E846E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr6:90577199 G>A maps to NM_012115.3 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr6:90577199 G>A maps to NM_012115.3 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:23309679 C>T maps to ENST00000435486 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:23309679 C>T maps to ENST00000435486 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:30890150 A>G maps to NM_032222.2 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:30890150 A>G maps to NM_032222.2 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:113558441 T>A maps to NM_002711.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:113558441 T>A maps to NM_002711.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:140453140 A>T maps to NM_004333.4 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr7:140453140 A>T maps to NM_004333.4 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:2832078 G>A maps to NM_033225.5 G2878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:2832078 G>A maps to NM_033225.5 G2878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:11995986 G>A maps to NM_201402.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:11995986 G>A maps to NM_201402.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:52733123 A>C maps to NM_052937.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:52733123 A>C maps to NM_052937.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:108276566 T>C maps to NM_001146.3 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chr8:108276566 T>C maps to NM_001146.3 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chrX:123176496 T>C did not map to a codon.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chrX:123176496 T>C did not map to a codon.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chrX:132458559 G>A maps to NM_001448.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-0821-01A-01W-0424-08 chrX:132458559 G>A maps to NM_001448.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr1:190067204 C>T maps to NM_199051.1 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr1:190067204 C>T maps to NM_199051.1 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr11:64557669 G>A maps to NM_004579.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr11:64557669 G>A maps to NM_004579.2 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr12:55714592 G>A maps to NM_001005182.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr12:55714592 G>A maps to NM_001005182.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr14:57858238 T>G maps to NM_001011713.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr14:57858238 T>G maps to NM_001011713.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr2:33810355 G>A maps to ENST00000395190 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr2:33810355 G>A maps to ENST00000395190 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr21:46032292 C>T maps to NM_198695.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr21:46032292 C>T maps to NM_198695.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr22:39355651 G>A maps to NM_001193289.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr22:39355651 G>A maps to NM_001193289.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr3:49940448 G>A maps to NM_002447.2 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr3:49940448 G>A maps to NM_002447.2 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr4:8605775 C>T maps to NM_001014447.2 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr4:8605775 C>T maps to NM_001014447.2 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr5:45262442 C>T maps to NM_021072.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr5:45262442 C>T maps to NM_021072.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr5:113740367 C>T maps to NM_021614.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr5:113740367 C>T maps to NM_021614.2 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr5:162932706 G>A maps to NM_013283.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr5:162932706 G>A maps to NM_013283.3 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr6:25819768 G>A maps to NM_005074.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr6:25819768 G>A maps to NM_005074.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr7:113519262 A>G maps to NM_002711.3 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr7:113519262 A>G maps to NM_002711.3 N628N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr7:143657659 C>T maps to NM_012369.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr7:143657659 C>T maps to NM_012369.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr8:39607191 A>G maps to NM_001464.3 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr8:39607191 A>G maps to NM_001464.3 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr8:63985638 T>C maps to NM_000370.3 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr8:63985638 T>C maps to NM_000370.3 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr8:105263255 G>A maps to NM_001100117.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr8:105263255 G>A maps to NM_001100117.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr9:96079848 G>A maps to ENST00000297954 A2225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chr9:96079848 G>A maps to ENST00000297954 A2225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chrX:76711874 C>T maps to NM_003868.1 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chrX:76711874 C>T maps to NM_003868.1 Y71Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chrX:153050272 A>G maps to NM_014370.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chrX:153050272 A>G maps to NM_014370.3 E439E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chrX:154294042 G>A maps to NM_001018025.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-1597-01B-01D-1495-08 chrX:154294042 G>A maps to NM_001018025.3 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:44595023 G>A did not map to a codon.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:44595023 G>A did not map to a codon.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:145367750 A>T maps to NM_001039703.4 G3449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:145367750 A>T maps to NM_001039703.4 G3449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:207644109 C>A maps to NM_001006658.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:207644109 C>A maps to NM_001006658.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:235866228 G>A maps to NM_000081.2 R3398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr1:235866228 G>A maps to NM_000081.2 R3398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr10:89725041 A>G did not map to a codon.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr10:89725041 A>G did not map to a codon.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr11:3687642 G>A maps to NM_020402.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr11:3687642 G>A maps to NM_020402.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr11:92714700 C>T maps to NM_005959.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr11:92714700 C>T maps to NM_005959.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr12:120599766 A>T maps to NM_006836.1 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr12:120599766 A>T maps to NM_006836.1 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr13:77570065 A>G maps to NM_006493.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr13:77570065 A>G maps to NM_006493.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr14:94700062 T>A maps to NM_058237.1 L197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr14:94700062 T>A maps to NM_058237.1 L197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr14:105612832 G>A maps to NM_002226.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr14:105612832 G>A maps to NM_002226.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr17:27939202 T>A maps to NM_152345.4 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr17:27939202 T>A maps to NM_152345.4 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr18:70209242 C>T maps to NM_182511.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr18:70209242 C>T maps to NM_182511.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:17086955 T>C maps to ENST00000443236 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:17086955 T>C maps to ENST00000443236 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:17918747 C>T maps to NM_014256.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:17918747 C>T maps to NM_014256.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:21606456 T>C maps to NM_001076678.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:21606456 T>C maps to NM_001076678.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:51986388 G>A maps to NM_001080405.1 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:51986388 G>A maps to NM_001080405.1 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:56704063 G>A maps to NM_001080456.2 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr19:56704063 G>A maps to NM_001080456.2 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr2:162813660 A>T maps to NM_001178015.1 K902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr2:162813660 A>T maps to NM_001178015.1 K902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr3:52816071 C>T maps to NM_002215.2 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr3:52816071 C>T maps to NM_002215.2 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr4:164415797 C>T did not map to a codon.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr4:164415797 C>T did not map to a codon.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr5:16769270 C>T maps to NM_012334.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr5:16769270 C>T maps to NM_012334.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr5:147782002 A>G maps to NM_205836.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr5:147782002 A>G maps to NM_205836.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr6:97613245 G>A maps to NM_198468.2 R1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr6:97613245 G>A maps to NM_198468.2 R1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr8:24357713 C>A maps to ENST00000380789 C649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr8:24357713 C>A maps to ENST00000380789 C649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr9:4117962 G>A maps to NM_001042413.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chr9:4117962 G>A maps to NM_001042413.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chrX:89177575 G>A maps to NM_138960.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3649-01A-01D-1495-08 chrX:89177575 G>A maps to NM_138960.3 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr11:60231771 C>T maps to NM_152866.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr11:60231771 C>T maps to NM_152866.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr12:247989 C>T maps to NM_001170738.1 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr12:247989 C>T maps to NM_001170738.1 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr15:78921863 G>A maps to NM_000750.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr15:78921863 G>A maps to NM_000750.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr16:24372857 C>T maps to NM_006539.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr16:24372857 C>T maps to NM_006539.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr16:48210868 G>A maps to NM_032583.3 H1168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr16:48210868 G>A maps to NM_032583.3 H1168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:34072484 C>T maps to NM_139285.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:34072484 C>T maps to NM_139285.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:39919366 G>A maps to NM_021991.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:39919366 G>A maps to NM_021991.2 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:46607744 G>T maps to NM_002144.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:46607744 G>T maps to NM_002144.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:72539124 G>A maps to NM_006678.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr17:72539124 G>A maps to NM_006678.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr19:16790903 C>T maps to NM_024074.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr19:16790903 C>T maps to NM_024074.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr19:46116828 G>A maps to NM_001193268.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr19:46116828 G>A maps to NM_001193268.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr20:43042365 C>T maps to ENST00000338692 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr20:43042365 C>T maps to ENST00000338692 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr4:5461832 C>T maps to NM_018401.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr4:5461832 C>T maps to NM_018401.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr5:140704 C>T maps to NM_052909.3 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr5:140704 C>T maps to NM_052909.3 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr5:1216996 C>T maps to NM_001003841.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr5:1216996 C>T maps to NM_001003841.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr7:135376341 G>A maps to NM_012450.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr7:135376341 G>A maps to NM_012450.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr8:27456002 C>T maps to NM_001831.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr8:27456002 C>T maps to NM_001831.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr9:32630678 A>T maps to NM_153809.2 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr9:32630678 A>T maps to NM_153809.2 L1633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr9:107379534 G>A maps to NM_001001956.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chr9:107379534 G>A maps to NM_001001956.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chrX:1746634 C>T maps to NM_001171038.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chrX:1746634 C>T maps to NM_001171038.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chrX:15381368 G>A maps to NM_004469.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chrX:15381368 G>A maps to NM_004469.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chrX:154490212 C>A maps to NM_171998.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3650-01A-01D-1495-08 chrX:154490212 C>A maps to NM_171998.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr1:220359029 G>A maps to ENST00000358951 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr1:220359029 G>A maps to ENST00000358951 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr1:222705451 G>A maps to NM_024746.3 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr1:222705451 G>A maps to NM_024746.3 R527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr1:237947551 C>T maps to NM_001035.2 G4180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr1:237947551 C>T maps to NM_001035.2 G4180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr11:56949853 C>T maps to NM_001005210.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr11:56949853 C>T maps to NM_001005210.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr12:52448555 G>T maps to ENST00000360284 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr12:52448555 G>T maps to ENST00000360284 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr12:117217035 C>T maps to NM_001109903.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr12:117217035 C>T maps to NM_001109903.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr17:18052553 G>A maps to ENST00000205890 S2327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr17:18052553 G>A maps to ENST00000205890 S2327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr17:31107789 C>T maps to NM_015194.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr17:31107789 C>T maps to NM_015194.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr17:42335420 G>A maps to NM_000342.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr17:42335420 G>A maps to NM_000342.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr18:20564927 T>C maps to ENST00000360790 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr18:20564927 T>C maps to ENST00000360790 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr2:191236127 G>C maps to NM_002194.3 *400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr2:191236127 G>C maps to NM_002194.3 *400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr20:43851265 A>G maps to NM_003008.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr20:43851265 A>G maps to NM_003008.2 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr3:12880945 A>G maps to ENST00000273223 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr3:12880945 A>G maps to ENST00000273223 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr3:21606167 C>T maps to NM_024697.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr3:21606167 C>T maps to NM_024697.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr3:195515159 T>C maps to NM_018406.5 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr3:195515159 T>C maps to NM_018406.5 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr4:6578363 C>T maps to NM_015274.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr4:6578363 C>T maps to NM_015274.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr4:39435837 G>A maps to NM_175737.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr4:39435837 G>A maps to NM_175737.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr5:26902768 G>A maps to NM_016279.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr5:26902768 G>A maps to NM_016279.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr5:89943465 A>G maps to NM_032119.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr5:89943465 A>G maps to NM_032119.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr5:140256667 G>A maps to NM_018903.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr5:140256667 G>A maps to NM_018903.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr6:100838895 G>A maps to ENST00000262901 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr6:100838895 G>A maps to ENST00000262901 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr6:169064763 T>C maps to NM_022138.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr6:169064763 T>C maps to NM_022138.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr7:141734060 G>T did not map to a codon.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr7:141734060 G>T did not map to a codon.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr8:139164562 G>A maps to NM_015912.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr8:139164562 G>A maps to NM_015912.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr9:96051415 A>G maps to ENST00000297954 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chr9:96051415 A>G maps to ENST00000297954 P1497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chrX:66937440 C>T maps to NM_000044.2 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3652-01A-01D-1495-08 chrX:66937440 C>T maps to NM_000044.2 F765F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr1:165177350 G>A maps to NM_177398.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr1:165177350 G>A maps to NM_177398.3 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr12:5603769 G>A maps to NM_001102654.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr12:5603769 G>A maps to NM_001102654.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr15:51041868 A>G maps to NM_032802.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr15:51041868 A>G maps to NM_032802.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr17:38635987 C>T maps to NM_032865.5 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr17:38635987 C>T maps to NM_032865.5 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr2:179323289 C>T maps to NM_001042702.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr2:179323289 C>T maps to NM_001042702.3 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr3:195965645 G>A maps to NM_005017.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr3:195965645 G>A maps to NM_005017.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr7:98256631 C>T maps to NM_002523.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr7:98256631 C>T maps to NM_002523.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr8:135612747 G>A maps to NM_020863.3 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr8:135612747 G>A maps to NM_020863.3 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr9:98683551 T>G maps to NM_001010895.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-3653-01A-01D-1495-08 chr9:98683551 T>G maps to NM_001010895.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr1:41285880 C>T maps to NM_004700.3 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr1:41285880 C>T maps to NM_004700.3 H330H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr1:156532967 C>T maps to NM_178229.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr1:156532967 C>T maps to NM_178229.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr10:115947724 A>G maps to NM_198795.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr10:115947724 A>G maps to NM_198795.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr12:65633733 G>A maps to NM_014319.4 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr12:65633733 G>A maps to NM_014319.4 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr12:69985893 T>G maps to NM_006431.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr12:69985893 T>G maps to NM_006431.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr12:125294729 C>A maps to NM_005505.4 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr12:125294729 C>A maps to NM_005505.4 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr14:74203799 G>A maps to NM_001043318.1 D550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr14:74203799 G>A maps to NM_001043318.1 D550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr15:30000962 G>A maps to NM_003257.3 H1550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr15:30000962 G>A maps to NM_003257.3 H1550H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr15:92690224 C>T maps to NM_013272.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr15:92690224 C>T maps to NM_013272.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr16:1129428 C>T maps to NM_001053.3 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr16:1129428 C>T maps to NM_001053.3 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr19:41600896 C>T maps to NM_000766.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr19:41600896 C>T maps to NM_000766.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr19:49862739 G>A maps to NM_003598.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr19:49862739 G>A maps to NM_003598.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr2:88828847 G>A maps to NM_152670.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr2:88828847 G>A maps to NM_152670.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr3:140866044 G>A maps to NM_080862.1 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr3:140866044 G>A maps to NM_080862.1 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr4:15938123 G>T maps to NM_005130.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr4:15938123 G>T maps to NM_005130.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr4:41621352 G>A maps to NM_014988.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr4:41621352 G>A maps to NM_014988.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr4:70080047 A>C maps to NM_001073.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr4:70080047 A>C maps to NM_001073.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr6:30035219 C>A maps to NM_021959.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr6:30035219 C>A maps to NM_021959.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr7:43622865 C>T maps to NM_004760.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr7:43622865 C>T maps to NM_004760.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr7:143826810 C>T maps to NM_001001659.1 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr7:143826810 C>T maps to NM_001001659.1 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr8:13251147 G>A maps to NM_182643.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr8:13251147 G>A maps to NM_182643.2 R410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr9:14789085 G>A maps to ENST00000380880 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr9:14789085 G>A maps to ENST00000380880 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr9:27204999 G>A maps to NM_000459.3 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chr9:27204999 G>A maps to NM_000459.3 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chrX:153716307 C>A maps to ENST00000440701 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5295-01A-01D-1486-08 chrX:153716307 C>A maps to ENST00000440701 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr1:24857821 C>T maps to NM_013441.2 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr1:24857821 C>T maps to NM_013441.2 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr1:152187696 G>A maps to NM_001009931.1 H2136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr1:152187696 G>A maps to NM_001009931.1 H2136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr1:204170870 C>T maps to NM_198447.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr1:204170870 C>T maps to NM_198447.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr11:117985880 G>A maps to NM_019894.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr11:117985880 G>A maps to NM_019894.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr11:120168972 G>C did not map to a codon.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr11:120168972 G>C did not map to a codon.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr12:95425194 G>A maps to NM_003297.2 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr12:95425194 G>A maps to NM_003297.2 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr17:39262035 C>T maps to ENST00000377731 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr17:39262035 C>T maps to ENST00000377731 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr17:74017965 G>A maps to NM_001988.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr17:74017965 G>A maps to NM_001988.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr17:79682530 C>T maps to ENST00000331531 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr17:79682530 C>T maps to ENST00000331531 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr2:102791959 C>T maps to NM_000877.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr2:102791959 C>T maps to NM_000877.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr2:190603403 G>A maps to NM_144708.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr2:190603403 G>A maps to NM_144708.3 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr5:140181795 C>T maps to NM_018906.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr5:140181795 C>T maps to NM_018906.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr6:25917029 T>A maps to NM_005835.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr6:25917029 T>A maps to NM_005835.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr7:4116750 C>T maps to NM_152744.3 D1044D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr7:4116750 C>T maps to NM_152744.3 D1044D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr7:75517606 G>T maps to NM_001040456.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr7:75517606 G>T maps to NM_001040456.1 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr7:150649545 G>A maps to NM_000238.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chr7:150649545 G>A maps to NM_000238.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chrX:23953459 C>T maps to NM_152761.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chrX:23953459 C>T maps to NM_152761.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chrX:47842385 G>A maps to NM_006962.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5299-01A-02D-1486-08 chrX:47842385 G>A maps to NM_006962.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:153004853 C>G maps to NM_003125.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:153004853 C>G maps to NM_003125.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:171080060 C>T maps to NM_006894.5 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:171080060 C>T maps to NM_006894.5 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:175067711 C>T maps to NM_022093.1 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:175067711 C>T maps to NM_022093.1 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:248790296 A>G maps to NM_001001964.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr1:248790296 A>G maps to NM_001001964.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr10:11908648 G>A maps to NM_153256.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr10:11908648 G>A maps to NM_153256.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr10:47087736 C>T maps to NM_005972.4 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr10:47087736 C>T maps to NM_005972.4 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr10:131755520 C>G did not map to a codon.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr10:131755520 C>G did not map to a codon.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr11:6977375 C>T maps to NM_013250.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr11:6977375 C>T maps to NM_013250.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr12:32763710 A>G maps to NM_139241.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr12:32763710 A>G maps to NM_139241.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr12:101295583 A>G maps to ENST00000392977 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr12:101295583 A>G maps to ENST00000392977 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr14:21826559 C>T maps to NM_007192.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr14:21826559 C>T maps to NM_007192.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr14:25044565 C>T maps to NM_001911.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr14:25044565 C>T maps to NM_001911.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr15:90348338 G>C maps to NM_001150.2 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr15:90348338 G>C maps to NM_001150.2 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr16:1306607 C>T maps to NM_012217.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr16:1306607 C>T maps to NM_012217.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr16:24552108 A>G maps to NM_006910.4 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr16:24552108 A>G maps to NM_006910.4 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr17:78082608 G>T maps to NM_001079804.1 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr17:78082608 G>T maps to NM_001079804.1 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr18:13826366 G>T maps to NM_005913.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr18:13826366 G>T maps to NM_005913.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr18:55328472 C>T maps to NM_005603.4 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr18:55328472 C>T maps to NM_005603.4 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr19:36219961 G>A maps to NM_014727.1 G1588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr19:36219961 G>A maps to NM_014727.1 G1588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr19:54314123 G>A maps to ENST00000391773 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr19:54314123 G>A maps to ENST00000391773 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr2:103095703 C>T maps to NM_001011552.3 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr2:103095703 C>T maps to NM_001011552.3 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr3:14861426 G>A maps to NM_152536.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr3:14861426 G>A maps to NM_152536.3 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr3:36874401 C>T maps to NM_014831.2 S2180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr3:36874401 C>T maps to NM_014831.2 S2180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr3:111846907 T>C maps to NM_001190259.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr3:111846907 T>C maps to NM_001190259.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr4:680076 C>T maps to ENST00000404286 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr4:680076 C>T maps to ENST00000404286 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr5:127623045 C>T maps to NM_001999.3 T2278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr5:127623045 C>T maps to NM_001999.3 T2278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr5:140052369 G>A maps to NM_194249.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr5:140052369 G>A maps to NM_194249.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr9:32784816 C>T maps to NM_212558.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr9:32784816 C>T maps to NM_212558.2 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr9:36170860 C>T maps to NM_005893.2 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr9:36170860 C>T maps to NM_005893.2 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr9:140127305 C>T maps to NM_080877.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chr9:140127305 C>T maps to NM_080877.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chrX:138643735 C>T maps to NM_000133.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-12-5301-01A-01D-1486-08 chrX:138643735 C>T maps to NM_000133.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr1:63001285 C>A maps to ENST00000371140 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr1:63001285 C>A maps to ENST00000371140 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr1:117699372 G>A maps to NM_024626.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr1:117699372 G>A maps to NM_024626.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr1:145440099 G>A maps to NM_006472.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr1:145440099 G>A maps to NM_006472.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr10:96443659 G>A maps to NM_000772.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr10:96443659 G>A maps to NM_000772.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr10:124066796 T>A maps to ENST00000368994 Y296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr10:124066796 T>A maps to ENST00000368994 Y296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr12:85255644 T>A maps to NM_182767.4 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr12:85255644 T>A maps to NM_182767.4 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr15:100537640 G>A maps to NM_139057.2 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr15:100537640 G>A maps to NM_139057.2 S915S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr17:34416596 C>T maps to NM_002983.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr17:34416596 C>T maps to NM_002983.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr19:9077405 C>T maps to NM_024690.2 W3347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr19:9077405 C>T maps to NM_024690.2 W3347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr19:54312881 G>A maps to ENST00000391773 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr19:54312881 G>A maps to ENST00000391773 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr3:51690164 C>T maps to NM_015106.2 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr3:51690164 C>T maps to NM_015106.2 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr5:1494824 C>A maps to NM_024830.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr5:1494824 C>A maps to NM_024830.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr5:53751846 C>T maps to NM_006308.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr5:53751846 C>T maps to NM_006308.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr5:180377066 C>T maps to NM_001040462.2 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr5:180377066 C>T maps to NM_001040462.2 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr6:17772258 G>A maps to NM_022113.4 T1452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr6:17772258 G>A maps to NM_022113.4 T1452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr8:95264451 C>T did not map to a codon.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr8:95264451 C>T did not map to a codon.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr9:101788193 G>A maps to NM_001855.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chr9:101788193 G>A maps to NM_001855.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chrX:16142165 G>A maps to NM_005314.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chrX:16142165 G>A maps to NM_005314.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chrX:151283895 C>T maps to NM_021049.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chrX:151283895 C>T maps to NM_021049.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chrX:153490644 C>T maps to NM_000513.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0740-01B-01D-1845-08 chrX:153490644 C>T maps to NM_000513.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr11:67765219 C>T maps to NM_030930.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr11:67765219 C>T maps to NM_030930.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr11:102646041 G>A maps to NM_002425.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr11:102646041 G>A maps to NM_002425.2 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr12:97085018 C>T maps to ENST00000342887 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr12:97085018 C>T maps to ENST00000342887 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr14:88478096 G>A maps to NM_003608.3 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr14:88478096 G>A maps to NM_003608.3 W302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr15:101595205 C>T maps to NM_024652.3 I1370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr15:101595205 C>T maps to NM_024652.3 I1370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr16:27225036 C>T maps to NM_001145348.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr16:27225036 C>T maps to NM_001145348.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr16:75564021 G>A maps to NM_024533.3 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr16:75564021 G>A maps to NM_024533.3 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr2:192711669 G>A did not map to a codon.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr2:192711669 G>A did not map to a codon.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr21:45732951 C>T maps to NM_002626.4 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr21:45732951 C>T maps to NM_002626.4 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr22:44536021 C>T maps to NM_001003828.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr22:44536021 C>T maps to NM_001003828.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr5:422881 C>T maps to NM_020731.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr5:422881 C>T maps to NM_020731.3 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr6:158579374 G>A maps to NM_032861.3 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0781-01B-01D-1696-08 chr6:158579374 G>A maps to NM_032861.3 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr1:147380345 G>A maps to NM_005267.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr1:147380345 G>A maps to NM_005267.4 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr11:22215064 G>A maps to NM_213599.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr11:22215064 G>A maps to NM_213599.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr11:48346803 T>C maps to NM_001004702.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr11:48346803 T>C maps to NM_001004702.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr11:59480720 G>A maps to NM_001005324.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr11:59480720 G>A maps to NM_001005324.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr12:62777953 T>C maps to ENST00000280377 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr12:62777953 T>C maps to ENST00000280377 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr14:70926318 C>T maps to NM_003813.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr14:70926318 C>T maps to NM_003813.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr19:46003205 G>C did not map to a codon.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr19:46003205 G>C did not map to a codon.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr21:43803236 G>A maps to ENST00000380399 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr21:43803236 G>A maps to ENST00000380399 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr3:15079600 C>G maps to NM_003298.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr3:15079600 C>G maps to NM_003298.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr4:102946613 G>A maps to NM_017935.4 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr4:102946613 G>A maps to NM_017935.4 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr6:25726719 G>A maps to NM_170745.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr6:25726719 G>A maps to NM_170745.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr7:106829792 C>T maps to NM_012257.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chr7:106829792 C>T maps to NM_012257.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chrX:48209557 C>T did not map to a codon.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chrX:48209557 C>T did not map to a codon.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chrX:118222576 G>A maps to NM_020721.1 D872D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0786-01B-01D-1492-08 chrX:118222576 G>A maps to NM_020721.1 D872D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr1:38435289 C>A maps to NM_006802.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr1:38435289 C>A maps to NM_006802.2 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr11:55904447 C>T maps to NM_001004064.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr11:55904447 C>T maps to NM_001004064.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr12:6464464 G>A maps to NM_001159576.1 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr12:6464464 G>A maps to NM_001159576.1 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr12:78574730 G>A maps to NM_014903.4 P1844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr12:78574730 G>A maps to NM_014903.4 P1844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr15:24921535 C>T maps to NM_018958.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr15:24921535 C>T maps to NM_018958.2 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr18:63476947 T>C maps to NM_004361.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr18:63476947 T>C maps to NM_004361.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr19:3449018 G>A maps to ENST00000269778 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr19:3449018 G>A maps to ENST00000269778 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr2:202401016 G>A maps to NM_001168221.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr2:202401016 G>A maps to NM_001168221.1 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr2:242142863 C>T maps to NM_001001891.3 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr2:242142863 C>T maps to NM_001001891.3 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr22:39357612 C>T maps to NM_001193289.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr22:39357612 C>T maps to NM_001193289.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr4:48569355 C>T maps to NM_015030.1 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr4:48569355 C>T maps to NM_015030.1 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr4:76722292 A>G maps to NM_003715.2 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr4:76722292 A>G maps to NM_003715.2 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr5:150922878 C>T maps to NM_001447.2 P2603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr5:150922878 C>T maps to NM_001447.2 P2603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr7:95019498 A>G maps to NM_000940.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr7:95019498 A>G maps to NM_000940.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr7:131872360 C>T maps to NM_020911.1 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0787-01A-01W-0424-08 chr7:131872360 C>T maps to NM_020911.1 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:19584461 C>T maps to NM_016183.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:19584461 C>T maps to NM_016183.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:144886203 C>T maps to NM_014644.4 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:144886203 C>T maps to NM_014644.4 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:151774394 G>A maps to NM_001004432.2 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:151774394 G>A maps to NM_001004432.2 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:153390659 G>A maps to NM_176823.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:153390659 G>A maps to NM_176823.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:186052022 C>A maps to NM_031935.2 I2938I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:186052022 C>A maps to NM_031935.2 I2938I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:222713492 G>A maps to NM_024746.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr1:222713492 G>A maps to NM_024746.3 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr11:20448404 G>A maps to NM_005788.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr11:20448404 G>A maps to NM_005788.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr11:117985880 G>A maps to NM_019894.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr11:117985880 G>A maps to NM_019894.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr11:120998872 C>T maps to NM_005422.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr11:120998872 C>T maps to NM_005422.2 Y729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr12:52309922 G>A maps to NM_001077401.1 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr12:52309922 G>A maps to NM_001077401.1 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr12:53687194 C>T maps to NM_012291.4 P2100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr12:53687194 C>T maps to NM_012291.4 P2100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr14:92470680 C>T maps to NM_004239.3 K1213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr14:92470680 C>T maps to NM_004239.3 K1213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr15:26793161 G>T maps to NM_021912.4 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr15:26793161 G>T maps to NM_021912.4 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr16:3021624 C>A maps to NM_152341.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr16:3021624 C>A maps to NM_152341.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr17:29556480 C>T maps to NM_001042492.2 Q950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr17:29556480 C>T maps to NM_001042492.2 Q950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr18:14542737 A>G maps to ENST00000444806 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr18:14542737 A>G maps to ENST00000444806 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr18:56587753 C>T maps to NM_018181.4 D745D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr18:56587753 C>T maps to NM_018181.4 D745D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr18:74154335 G>A maps to ENST00000443185 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr18:74154335 G>A maps to ENST00000443185 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr19:14591539 C>G maps to NM_202470.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr19:14591539 C>G maps to NM_202470.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr19:50243158 G>A maps to NM_021733.1 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr19:50243158 G>A maps to NM_021733.1 H551H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr19:55385634 C>T did not map to a codon.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr19:55385634 C>T did not map to a codon.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr2:234545194 C>T maps to NM_019075.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr2:234545194 C>T maps to NM_019075.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr4:995506 C>T maps to NM_000203.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr4:995506 C>T maps to NM_000203.3 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr4:88420672 C>T maps to NM_004684.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr4:88420672 C>T maps to NM_004684.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr4:155507296 G>T maps to NM_000508.3 Y428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr4:155507296 G>T maps to NM_000508.3 Y428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr5:140174749 G>A maps to NM_018905.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr5:140174749 G>A maps to NM_018905.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:32118159 G>A maps to NM_030651.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:32118159 G>A maps to NM_030651.3 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:33633621 C>T maps to ENST00000374316 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:33633621 C>T maps to ENST00000374316 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:43748478 C>T maps to NM_001025366.2 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:43748478 C>T maps to NM_001025366.2 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:161020530 C>T did not map to a codon.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr6:161020530 C>T did not map to a codon.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr7:87092143 G>T maps to NM_018849.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr7:87092143 G>T maps to NM_018849.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr9:127566376 C>T maps to NM_182487.2 N308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr9:127566376 C>T maps to NM_182487.2 N308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr9:136507480 C>T maps to NM_000787.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chr9:136507480 C>T maps to NM_000787.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chrX:12904280 C>T maps to NM_016562.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0789-01A-01W-0424-08 chrX:12904280 C>T maps to NM_016562.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr1:118628590 A>C maps to NM_206996.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr1:118628590 A>C maps to NM_206996.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr10:63957756 G>T maps to NM_145307.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr10:63957756 G>T maps to NM_145307.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr10:101981867 C>T did not map to a codon.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr10:101981867 C>T did not map to a codon.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr12:53185579 C>T maps to ENST00000309505 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr12:53185579 C>T maps to ENST00000309505 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr12:123794338 C>T maps to NM_001167856.1 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr12:123794338 C>T maps to NM_001167856.1 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr13:49865830 A>C maps to NM_030911.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr13:49865830 A>C maps to NM_030911.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr13:103343255 G>A maps to NM_001010977.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr13:103343255 G>A maps to NM_001010977.1 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr16:61687973 C>T maps to NM_001796.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr16:61687973 C>T maps to NM_001796.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr16:89782934 G>C maps to NM_004913.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr16:89782934 G>C maps to NM_004913.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr17:10369589 G>A maps to NM_017533.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr17:10369589 G>A maps to NM_017533.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr17:31351021 C>T maps to NM_183377.1 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr17:31351021 C>T maps to NM_183377.1 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr19:19351445 C>T maps to NM_004386.2 N1148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr19:19351445 C>T maps to NM_004386.2 N1148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr19:55284914 C>T maps to ENST00000291633 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr19:55284914 C>T maps to ENST00000291633 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr19:58565271 C>T maps to NM_182572.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr19:58565271 C>T maps to NM_182572.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr2:8943254 A>G maps to NM_020738.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr2:8943254 A>G maps to NM_020738.2 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr2:109292447 C>T maps to NM_001193484.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr2:109292447 C>T maps to NM_001193484.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr3:42916849 C>T maps to NM_004391.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr3:42916849 C>T maps to NM_004391.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr3:123376129 C>T maps to NM_053025.3 T1377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr3:123376129 C>T maps to NM_053025.3 T1377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr5:147781653 G>A maps to NM_205836.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr5:147781653 G>A maps to NM_205836.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr6:146755475 C>A maps to NM_000838.3 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr6:146755475 C>A maps to NM_000838.3 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr7:107575936 G>A maps to NM_002291.2 Q1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr7:107575936 G>A maps to NM_002291.2 Q1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr9:116750723 C>T maps to ENST00000374126 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chr9:116750723 C>T maps to ENST00000374126 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chrX:11160413 G>A maps to NM_013427.2 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chrX:11160413 G>A maps to NM_013427.2 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chrX:18348707 C>T maps to NM_006089.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chrX:18348707 C>T maps to NM_006089.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chrX:129149264 G>A maps to ENST00000303743 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0790-01B-01D-1494-08 chrX:129149264 G>A maps to ENST00000303743 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:11107016 G>A maps to NM_006610.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:11107016 G>A maps to NM_006610.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:156816383 C>T maps to NM_014215.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:156816383 C>T maps to NM_014215.2 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:158576315 T>C maps to NM_001004478.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:158576315 T>C maps to NM_001004478.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:232581432 C>T maps to NM_020808.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr1:232581432 C>T maps to NM_020808.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr10:48413955 C>T maps to NM_016204.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr10:48413955 C>T maps to NM_016204.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr10:102676870 C>T maps to NM_001136123.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr10:102676870 C>T maps to NM_001136123.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr11:32954285 G>A maps to NM_001076786.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr11:32954285 G>A maps to NM_001076786.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr11:59807825 C>T did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr11:59807825 C>T did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr12:113730817 G>C maps to NM_001143819.1 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr12:113730817 G>C maps to NM_001143819.1 R803R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr15:23811196 C>T maps to NM_005664.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr15:23811196 C>T maps to NM_005664.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr15:84245408 C>T maps to ENST00000434347 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr15:84245408 C>T maps to ENST00000434347 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr17:15517207 C>T maps to ENST00000455584 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr17:15517207 C>T maps to ENST00000455584 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr18:20573448 C>G maps to ENST00000360790 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr18:20573448 C>G maps to ENST00000360790 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr18:23738209 T>A did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr18:23738209 T>A did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:25965917 C>T maps to NM_018263.4 Q1096Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:25965917 C>T maps to NM_018263.4 Q1096Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:173338969 G>A maps to ENST00000264106 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:173338969 G>A maps to ENST00000264106 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:233246042 C>T maps to NM_001632.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:233246042 C>T maps to NM_001632.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:238275873 C>T maps to NM_004369.3 R1652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:238275873 C>T maps to NM_004369.3 R1652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:240969714 G>T maps to NM_001005853.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr2:240969714 G>T maps to NM_001005853.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr20:55777536 G>A maps to NM_001719.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr20:55777536 G>A maps to NM_001719.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr22:36983510 C>T did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr22:36983510 C>T did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr3:139297856 G>A maps to ENST00000296202 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr3:139297856 G>A maps to ENST00000296202 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr3:182897227 C>T maps to NM_015078.2 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr3:182897227 C>T maps to NM_015078.2 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:30724195 G>T maps to NM_001173523.1 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:30724195 G>T maps to NM_001173523.1 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:71847740 A>G maps to ENST00000396051 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:71847740 A>G maps to ENST00000396051 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:103184236 G>A maps to NM_001135146.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:103184236 G>A maps to NM_001135146.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:110880564 C>A maps to NM_001963.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:110880564 C>A maps to NM_001963.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:141578364 C>T maps to NM_015130.2 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr4:141578364 C>T maps to NM_015130.2 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr6:7585168 T>A maps to NM_004415.2 A2558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr6:7585168 T>A maps to NM_004415.2 A2558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr6:44255397 C>T maps to NM_182539.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr6:44255397 C>T maps to NM_182539.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr7:44714132 C>T maps to ENST00000444676 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr7:44714132 C>T maps to ENST00000444676 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr8:125110058 A>G maps to NM_001039112.2 E1606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr8:125110058 A>G maps to NM_001039112.2 E1606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr9:14155893 T>A did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr9:14155893 T>A did not map to a codon.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr9:18777208 C>G maps to NM_001040272.4 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chr9:18777208 C>G maps to NM_001040272.4 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chrX:147743982 C>T maps to NM_002025.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0813-01A-01W-0424-08 chrX:147743982 C>T maps to NM_002025.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr1:92224220 C>T maps to NM_003243.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr1:92224220 C>T maps to NM_003243.4 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr10:127677131 G>A maps to ENST00000368692 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr10:127677131 G>A maps to ENST00000368692 T68T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-14-0817-01A-01W-0424-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-14-0817-01A-01W-0424-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr11:26734240 G>A maps to NM_178498.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr11:26734240 G>A maps to NM_178498.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr11:73073627 G>A maps to NM_014786.3 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr11:73073627 G>A maps to NM_014786.3 S1615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr12:9346768 G>A maps to NM_002864.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr12:9346768 G>A maps to NM_002864.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr13:53029667 C>T did not map to a codon.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr13:53029667 C>T did not map to a codon.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr14:65261275 C>T maps to ENST00000389723 Q572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr14:65261275 C>T maps to ENST00000389723 Q572Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr14:69702869 G>T did not map to a codon.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr14:69702869 G>T did not map to a codon.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr15:42700425 G>A maps to NM_000070.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr15:42700425 G>A maps to NM_000070.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr15:89401857 A>G maps to NM_013227.3 V2014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr15:89401857 A>G maps to NM_013227.3 V2014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr17:10447063 G>A maps to NM_017534.5 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr17:10447063 G>A maps to NM_017534.5 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr18:29038466 C>A maps to NM_001944.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr18:29038466 C>A maps to NM_001944.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr2:198968640 G>A maps to NM_006226.3 W1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr2:198968640 G>A maps to NM_006226.3 W1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr20:9370527 T>C maps to NM_001172646.1 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr20:9370527 T>C maps to NM_001172646.1 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr20:44417584 G>A maps to NM_080614.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr20:44417584 G>A maps to NM_080614.1 R66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr21:43161459 G>A maps to ENST00000352483 N679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr21:43161459 G>A maps to ENST00000352483 N679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr3:127682173 C>T maps to NM_207335.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr3:127682173 C>T maps to NM_207335.2 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr6:87725078 G>A maps to NM_000865.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr6:87725078 G>A maps to NM_000865.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr6:146720757 C>T maps to NM_000838.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr6:146720757 C>T maps to NM_000838.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr7:98254300 C>T maps to NM_002523.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr7:98254300 C>T maps to NM_002523.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr8:70744224 G>A maps to NM_030958.2 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0817-01A-01W-0424-08 chr8:70744224 G>A maps to NM_030958.2 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr12:6128779 G>A maps to NM_000552.3 H1268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr12:6128779 G>A maps to NM_000552.3 H1268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr15:50788097 T>C maps to NM_005154.3 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr15:50788097 T>C maps to NM_005154.3 F904F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr17:9066305 A>T maps to NM_004822.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr17:9066305 A>T maps to NM_004822.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr17:76128875 G>A maps to NM_152468.4 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr17:76128875 G>A maps to NM_152468.4 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:3113329 C>T maps to NM_002067.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:3113329 C>T maps to NM_002067.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:7593589 G>A did not map to a codon.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:7593589 G>A did not map to a codon.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:15484622 A>G maps to NM_005858.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:15484622 A>G maps to NM_005858.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:40363234 C>T maps to NM_003890.2 V4945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr19:40363234 C>T maps to NM_003890.2 V4945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr2:135738920 G>T maps to NM_025052.3 C1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr2:135738920 G>T maps to NM_025052.3 C1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr2:234237129 C>T maps to NM_000541.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr2:234237129 C>T maps to NM_000541.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr20:49626629 G>A maps to NM_002237.3 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr20:49626629 G>A maps to NM_002237.3 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr3:53222822 G>A maps to NM_212539.1 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr3:53222822 G>A maps to NM_212539.1 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr3:108076823 C>T maps to NM_007072.2 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr3:108076823 C>T maps to NM_007072.2 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr5:139060957 C>T maps to NM_016463.7 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr5:139060957 C>T maps to NM_016463.7 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr6:129687470 C>T maps to NM_000426.3 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr6:129687470 C>T maps to NM_000426.3 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr7:147914500 G>A maps to NM_014141.5 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr7:147914500 G>A maps to NM_014141.5 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr9:125424623 G>A maps to ENST00000373686 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0862-01B-01D-1845-08 chr9:125424623 G>A maps to ENST00000373686 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr1:158986411 C>G maps to ENST00000295809 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr1:158986411 C>G maps to ENST00000295809 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr11:59376013 G>A maps to NM_002556.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr11:59376013 G>A maps to NM_002556.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr12:125296421 C>T maps to NM_005505.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr12:125296421 C>T maps to NM_005505.4 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr12:126138506 G>T maps to NM_052907.2 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr12:126138506 G>T maps to NM_052907.2 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr14:69349622 G>A maps to NM_001130004.1 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr14:69349622 G>A maps to NM_001130004.1 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr16:53528140 G>A maps to ENST00000425875 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr16:53528140 G>A maps to ENST00000425875 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr17:29557335 C>T maps to NM_001042492.2 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr17:29557335 C>T maps to NM_001042492.2 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr19:30476135 G>A maps to NM_003796.2 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr19:30476135 G>A maps to NM_003796.2 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr19:57088456 A>G maps to NM_001001668.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr19:57088456 A>G maps to NM_001001668.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr2:69046426 T>C maps to NM_001007231.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr2:69046426 T>C maps to NM_001007231.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr2:97400182 G>C maps to NM_001142292.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr2:97400182 G>C maps to NM_001142292.1 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr3:88205313 G>A maps to NM_173824.3 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr3:88205313 G>A maps to NM_173824.3 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr3:195969478 A>C maps to NM_005017.2 Y173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr3:195969478 A>C maps to NM_005017.2 Y173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr4:185631266 A>G maps to NM_024629.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr4:185631266 A>G maps to NM_024629.3 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr6:656374 G>A maps to NM_148959.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chr6:656374 G>A maps to NM_148959.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chrX:151808910 G>A maps to NM_018558.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-0871-01A-01W-0424-08 chrX:151808910 G>A maps to NM_018558.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr1:155291138 G>A maps to NM_001039517.1 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr1:155291138 G>A maps to NM_001039517.1 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr1:179989185 C>G maps to NM_014810.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr1:179989185 C>G maps to NM_014810.4 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr12:107048020 T>G maps to ENST00000357881 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr12:107048020 T>G maps to ENST00000357881 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr15:75641494 C>T maps to NM_024608.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr15:75641494 C>T maps to NM_024608.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr17:3779537 G>A maps to ENST00000381771 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr17:3779537 G>A maps to ENST00000381771 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr19:9062383 G>T maps to NM_024690.2 T8354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr19:9062383 G>T maps to NM_024690.2 T8354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr19:11594571 G>A maps to NM_138783.3 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr19:11594571 G>A maps to NM_138783.3 C591C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr3:99891167 G>A maps to NM_032359.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr3:99891167 G>A maps to NM_032359.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr5:75427790 C>T maps to NM_014979.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr5:75427790 C>T maps to NM_014979.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr9:116858750 G>A maps to ENST00000259410 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr9:116858750 G>A maps to ENST00000259410 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr11:61511462 C>T maps to NM_006133.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr11:61511462 C>T maps to NM_006133.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr11:89531774 T>C maps to NM_020358.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr11:89531774 T>C maps to NM_020358.2 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr11:129306838 G>A maps to NM_003658.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr11:129306838 G>A maps to NM_003658.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr12:47186770 G>A maps to NM_018018.4 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr12:47186770 G>A maps to NM_018018.4 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr12:130185157 G>A maps to NM_133448.2 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr12:130185157 G>A maps to NM_133448.2 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr14:104641822 C>T maps to NM_015656.1 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr14:104641822 C>T maps to NM_015656.1 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr15:72954611 G>A maps to NM_018652.4 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr15:72954611 G>A maps to NM_018652.4 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr16:81015431 C>T maps to NM_020188.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr16:81015431 C>T maps to NM_020188.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr17:40823100 G>A maps to NM_024927.4 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr17:40823100 G>A maps to NM_024927.4 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr18:44260325 C>T maps to NM_013305.4 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr18:44260325 C>T maps to NM_013305.4 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr19:44932747 G>A maps to NM_014518.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr19:44932747 G>A maps to NM_014518.2 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr2:169783710 A>T maps to NM_003742.2 A1191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr2:169783710 A>T maps to NM_003742.2 A1191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr2:241808651 C>T maps to NM_000030.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr2:241808651 C>T maps to NM_000030.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr3:169557942 G>A maps to NM_024727.2 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr3:169557942 G>A maps to NM_024727.2 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr4:70620980 T>C did not map to a codon.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr4:70620980 T>C did not map to a codon.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr4:113107977 C>T maps to NM_152400.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr4:113107977 C>T maps to NM_152400.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr5:637857 C>T maps to NM_018140.3 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr5:637857 C>T maps to NM_018140.3 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr7:100677498 G>A maps to NM_001040105.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr7:100677498 G>A maps to NM_001040105.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr9:43630641 G>A maps to NM_001145196.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr9:43630641 G>A maps to NM_001145196.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr9:137676833 G>T did not map to a codon.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chr9:137676833 G>T did not map to a codon.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chrX:140994695 T>A maps to NM_005462.4 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1395-01B-11D-1845-08 chrX:140994695 T>A maps to NM_005462.4 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr10:129905311 G>A maps to NM_002417.4 R1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr10:129905311 G>A maps to NM_002417.4 R1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr11:108788718 T>C maps to NM_004398.2 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr11:108788718 T>C maps to NM_004398.2 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr11:114453239 G>A maps to NM_001077639.1 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr11:114453239 G>A maps to NM_001077639.1 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr12:7848192 G>A maps to NM_020634.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr12:7848192 G>A maps to NM_020634.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr12:112622896 C>T maps to NM_001109662.2 S3119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr12:112622896 C>T maps to NM_001109662.2 S3119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr13:28919629 C>T maps to NM_002019.4 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr13:28919629 C>T maps to NM_002019.4 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr14:20871544 C>T maps to NM_007110.4 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr14:20871544 C>T maps to NM_007110.4 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr19:3959626 C>T maps to NM_001348.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr19:3959626 C>T maps to NM_001348.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr19:6416418 C>A did not map to a codon.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr19:6416418 C>A did not map to a codon.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr19:15272327 G>A maps to NM_000435.2 H2037H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr19:15272327 G>A maps to NM_000435.2 H2037H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr2:108443528 G>A maps to NM_182588.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr2:108443528 G>A maps to NM_182588.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr2:233274347 C>T maps to NM_031313.2 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr2:233274347 C>T maps to NM_031313.2 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr21:32638853 T>C maps to NM_003253.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr21:32638853 T>C maps to NM_003253.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr4:146576355 A>T maps to NM_172250.2 K343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr4:146576355 A>T maps to NM_172250.2 K343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr5:127671243 G>A maps to NM_001999.3 N1250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr5:127671243 G>A maps to NM_001999.3 N1250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr5:177547366 C>T maps to NM_015111.1 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr5:177547366 C>T maps to NM_015111.1 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr6:51918900 G>A maps to NM_138694.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr6:51918900 G>A maps to NM_138694.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr6:150464588 G>A maps to NM_030949.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr6:150464588 G>A maps to NM_030949.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr9:34996742 C>T maps to NM_001135005.1 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1450-01B-01D-1845-08 chr9:34996742 C>T maps to NM_001135005.1 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr13:49280991 C>T maps to NM_020377.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr13:49280991 C>T maps to NM_020377.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr15:85234815 C>T maps to NM_014300.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr15:85234815 C>T maps to NM_014300.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr7:55219020 C>T maps to NM_005228.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr7:55219020 C>T maps to NM_005228.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr8:145947814 G>A maps to NM_138367.1 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chr8:145947814 G>A maps to NM_138367.1 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chrX:79282294 C>A maps to NM_016954.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1456-01B-01D-1494-08 chrX:79282294 C>A maps to NM_016954.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr1:20992722 G>A maps to NM_020816.2 D965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr1:20992722 G>A maps to NM_020816.2 D965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr1:175372636 C>T maps to NM_003285.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr1:175372636 C>T maps to NM_003285.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr17:46805736 C>A maps to NM_006361.5 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr17:46805736 C>A maps to NM_006361.5 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr2:125405458 C>T maps to NM_130773.2 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr2:125405458 C>T maps to NM_130773.2 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr2:138033555 G>A maps to ENST00000272643 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr2:138033555 G>A maps to ENST00000272643 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr2:179730517 G>A maps to NM_173648.3 C900C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr2:179730517 G>A maps to NM_173648.3 C900C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr20:43938205 G>T did not map to a codon.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr20:43938205 G>T did not map to a codon.
Alternatively spliced codon TCGA-14-1823-01A-01W-0643-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-14-1823-01A-01W-0643-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr7:137263038 G>A maps to NM_004717.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr7:137263038 G>A maps to NM_004717.2 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr8:22006476 C>A maps to NM_139278.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr8:22006476 C>A maps to NM_139278.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr9:33351730 G>A maps to NM_002504.4 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr9:33351730 G>A maps to NM_002504.4 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr9:79867154 T>C maps to ENST00000376646 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chr9:79867154 T>C maps to ENST00000376646 D725D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chrX:69282973 C>T maps to NM_207320.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chrX:69282973 C>T maps to NM_207320.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chrX:78216460 C>T maps to NM_198333.1 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1823-01A-01W-0643-08 chrX:78216460 C>T maps to NM_198333.1 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr1:47685763 G>A maps to ENST00000371883 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr1:47685763 G>A maps to ENST00000371883 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr12:49420538 A>T maps to NM_003482.3 Y5070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr12:49420538 A>T maps to NM_003482.3 Y5070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr12:70983774 C>T maps to NM_001109754.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr12:70983774 C>T maps to NM_001109754.1 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr12:81101566 G>A maps to NM_002469.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr12:81101566 G>A maps to NM_002469.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr13:114079396 G>A maps to NM_138430.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr13:114079396 G>A maps to NM_138430.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr17:58711270 C>T maps to NM_003620.3 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr17:58711270 C>T maps to NM_003620.3 H253H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr18:2847911 C>T maps to NM_032048.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr18:2847911 C>T maps to NM_032048.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr18:44554652 G>A maps to NM_145653.3 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr18:44554652 G>A maps to NM_145653.3 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr2:168101234 G>A maps to NM_152381.5 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr2:168101234 G>A maps to NM_152381.5 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr2:179647000 G>A maps to NM_133378.4 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr2:179647000 G>A maps to NM_133378.4 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr20:51870233 C>T maps to NM_173485.5 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr20:51870233 C>T maps to NM_173485.5 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr20:54824417 C>T maps to ENST00000371389 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr20:54824417 C>T maps to ENST00000371389 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr3:15468121 C>T did not map to a codon.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr3:15468121 C>T did not map to a codon.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr4:71201280 C>T maps to NM_033122.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr4:71201280 C>T maps to NM_033122.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr4:155528019 G>A maps to ENST00000407946 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr4:155528019 G>A maps to ENST00000407946 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr5:1033571 C>G maps to NM_033120.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr5:1033571 C>G maps to NM_033120.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr8:17447274 G>A did not map to a codon.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chr8:17447274 G>A did not map to a codon.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chrX:54777769 C>T maps to NM_198510.2 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1825-01A-01W-0643-08 chrX:54777769 C>T maps to NM_198510.2 P1132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:11334001 C>G maps to NM_013319.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:11334001 C>G maps to NM_013319.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:33646781 G>C maps to NM_018207.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:33646781 G>C maps to NM_018207.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:205312606 G>A maps to NM_018203.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:205312606 G>A maps to NM_018203.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:222717501 G>A maps to NM_024746.3 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:222717501 G>A maps to NM_024746.3 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:229606470 G>A maps to NM_018230.2 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr1:229606470 G>A maps to NM_018230.2 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr10:49667896 G>A maps to ENST00000417912 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr10:49667896 G>A maps to ENST00000417912 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr10:98156949 C>T maps to NM_012465.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr10:98156949 C>T maps to NM_012465.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr12:6497970 C>T maps to NM_002342.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr12:6497970 C>T maps to NM_002342.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr13:46358033 G>A maps to NM_198849.2 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr13:46358033 G>A maps to NM_198849.2 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr14:102028606 C>T maps to NM_001362.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr14:102028606 C>T maps to NM_001362.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr15:49076317 C>T did not map to a codon.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr15:49076317 C>T did not map to a codon.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr17:18875007 G>A maps to NM_001039999.2 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr17:18875007 G>A maps to NM_001039999.2 D712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr17:21319358 G>A maps to NM_021012.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr17:21319358 G>A maps to NM_021012.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr19:18171937 C>A maps to NM_005535.1 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr19:18171937 C>A maps to NM_005535.1 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr2:242814084 C>T maps to NM_173821.2 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr2:242814084 C>T maps to NM_173821.2 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr4:20544132 T>C maps to ENST00000273739 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr4:20544132 T>C maps to ENST00000273739 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr5:137846887 T>C maps to NM_004730.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr5:137846887 T>C maps to NM_004730.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr7:43917036 G>C maps to NM_001077663.1 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr7:43917036 G>C maps to NM_001077663.1 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr7:99516655 G>A maps to NM_033017.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr7:99516655 G>A maps to NM_033017.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr7:106508125 C>T maps to NM_002649.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr7:106508125 C>T maps to NM_002649.2 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr8:120831591 G>C maps to NM_003184.3 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1829-01A-01W-0643-08 chr8:120831591 G>C maps to NM_003184.3 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr1:152058702 G>A maps to NM_001008536.1 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr1:152058702 G>A maps to NM_001008536.1 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr1:228479710 G>A maps to NM_001098623.1 G3484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr1:228479710 G>A maps to NM_001098623.1 G3484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr10:93038066 C>T maps to NM_032373.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr10:93038066 C>T maps to NM_032373.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr11:63585589 G>A maps to NM_138471.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr11:63585589 G>A maps to NM_138471.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr12:8672916 G>A maps to NM_080387.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr12:8672916 G>A maps to NM_080387.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr14:20979115 G>A maps to ENST00000430083 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr14:20979115 G>A maps to ENST00000430083 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr16:24358109 C>T maps to NM_006539.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr16:24358109 C>T maps to NM_006539.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr16:53671673 C>T maps to NM_015272.2 Q1051Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr16:53671673 C>T maps to NM_015272.2 Q1051Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr17:8053153 G>A maps to NM_002616.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr17:8053153 G>A maps to NM_002616.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:498514 C>A maps to NM_130760.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:498514 C>A maps to NM_130760.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:1068627 G>A maps to NM_012292.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:1068627 G>A maps to NM_012292.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:22155162 A>T maps to NM_007153.3 C891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:22155162 A>T maps to NM_007153.3 C891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:46127975 C>T did not map to a codon.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:46127975 C>T did not map to a codon.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:51633282 C>A maps to NM_014441.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr19:51633282 C>A maps to NM_014441.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr2:183094870 A>G maps to NM_005019.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr2:183094870 A>G maps to NM_005019.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr4:6594913 G>A maps to NM_015274.1 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr4:6594913 G>A maps to NM_015274.1 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr6:25726545 C>T maps to NM_170745.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr6:25726545 C>T maps to NM_170745.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr6:42976450 A>G maps to NM_006245.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr6:42976450 A>G maps to NM_006245.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr7:108524568 G>T maps to NM_001024607.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr7:108524568 G>T maps to NM_001024607.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr8:105361358 C>T maps to NM_030788.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr8:105361358 C>T maps to NM_030788.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr8:144801638 G>A maps to NM_139021.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr8:144801638 G>A maps to NM_139021.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr9:32784489 C>T maps to NM_212558.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chr9:32784489 C>T maps to NM_212558.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chrX:153581718 C>T maps to NM_001110556.1 P1989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-2554-01A-01D-1494-08 chrX:153581718 C>T maps to NM_001110556.1 P1989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr1:41289930 G>T did not map to a codon.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr1:41289930 G>T did not map to a codon.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr1:153391618 A>T did not map to a codon.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr1:153391618 A>T did not map to a codon.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr11:1270907 G>A maps to ENST00000447027 T4269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr11:1270907 G>A maps to ENST00000447027 T4269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr11:92532112 C>T maps to ENST00000298047 S1978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr11:92532112 C>T maps to ENST00000298047 S1978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr12:10233989 G>T maps to NM_016511.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr12:10233989 G>T maps to NM_016511.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr12:90024360 T>C maps to ENST00000428670 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr12:90024360 T>C maps to ENST00000428670 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr12:110825637 G>A maps to NM_016238.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr12:110825637 G>A maps to NM_016238.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr13:52439730 C>T maps to NM_031290.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr13:52439730 C>T maps to NM_031290.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr17:21206532 G>A maps to NM_145109.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr17:21206532 G>A maps to NM_145109.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr19:9084742 G>T maps to NM_024690.2 R2358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr19:9084742 G>T maps to NM_024690.2 R2358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr19:11136159 C>T maps to NM_001128849.1 H1048H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr19:11136159 C>T maps to NM_001128849.1 H1048H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr19:55451739 G>A maps to ENST00000446217 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr19:55451739 G>A maps to ENST00000446217 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr2:9347325 G>A maps to NM_003887.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr2:9347325 G>A maps to NM_003887.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr2:141143510 C>A maps to NM_018557.2 R3494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr2:141143510 C>A maps to NM_018557.2 R3494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr22:42910783 C>T maps to NM_015703.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr22:42910783 C>T maps to NM_015703.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr3:4699831 C>T maps to ENST00000356617 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr3:4699831 C>T maps to ENST00000356617 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr3:50416394 C>T maps to ENST00000435965 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr3:50416394 C>T maps to ENST00000435965 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr3:58520773 G>A maps to NM_003500.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr3:58520773 G>A maps to NM_003500.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr4:110915952 T>C maps to NM_001963.4 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr4:110915952 T>C maps to NM_001963.4 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr5:23522494 G>A maps to NM_020227.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr5:23522494 G>A maps to NM_020227.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr5:140202988 T>A maps to NM_018908.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr5:140202988 T>A maps to NM_018908.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr6:38256181 G>T maps to NM_052893.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr6:38256181 G>T maps to NM_052893.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr6:44198123 T>C maps to ENST00000313248 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr6:44198123 T>C maps to ENST00000313248 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr6:137482859 G>A maps to NM_052962.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr6:137482859 G>A maps to NM_052962.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr7:71275405 C>T maps to NM_031468.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr7:71275405 C>T maps to NM_031468.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr7:150417943 C>T maps to NM_130759.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chr7:150417943 C>T maps to NM_130759.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chrX:9905428 C>T maps to NM_001649.2 P1281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chrX:9905428 C>T maps to NM_001649.2 P1281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chrX:38009053 A>G maps to NM_006307.4 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chrX:38009053 A>G maps to NM_006307.4 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chrX:153416185 T>C maps to NM_020061.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-3476-01B-01D-1353-08 chrX:153416185 T>C maps to NM_020061.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr1:228004939 C>T maps to NM_183062.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr1:228004939 C>T maps to NM_183062.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr10:131676049 T>C maps to ENST00000355311 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr10:131676049 T>C maps to ENST00000355311 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr11:12902598 G>C did not map to a codon.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr11:12902598 G>C did not map to a codon.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr12:52565280 C>T maps to NM_182507.2 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr12:52565280 C>T maps to NM_182507.2 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr12:59271380 G>A maps to NM_153377.3 N779N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr12:59271380 G>A maps to NM_153377.3 N779N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr15:84442303 C>T maps to NM_207517.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr15:84442303 C>T maps to NM_207517.2 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr17:38253027 C>G maps to NM_021724.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr17:38253027 C>G maps to NM_021724.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr19:15839023 G>A maps to NM_013939.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr19:15839023 G>A maps to NM_013939.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr19:44351486 T>A maps to NM_181845.1 L245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr19:44351486 T>A maps to NM_181845.1 L245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr2:80085193 A>C maps to ENST00000402739 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr2:80085193 A>C maps to ENST00000402739 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr2:233613793 T>C did not map to a codon.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr2:233613793 T>C did not map to a codon.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr20:62577190 A>T maps to NM_017859.3 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr20:62577190 A>T maps to NM_017859.3 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr6:29080437 G>A maps to NM_001005216.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr6:29080437 G>A maps to NM_001005216.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr6:47512402 G>A maps to NM_012120.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr6:47512402 G>A maps to NM_012120.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr6:74149962 G>T maps to NM_138441.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr6:74149962 G>T maps to NM_138441.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr7:98588208 G>A maps to ENST00000359863 S3245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-4157-01A-01D-1353-08 chr7:98588208 G>A maps to ENST00000359863 S3245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr1:26507076 C>T maps to ENST00000374253 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr1:26507076 C>T maps to ENST00000374253 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr12:130927140 G>A maps to NM_015347.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr12:130927140 G>A maps to NM_015347.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr14:74969470 G>A maps to NM_000428.2 T1685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr14:74969470 G>A maps to NM_000428.2 T1685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr15:81282093 C>A maps to NM_015154.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr15:81282093 C>A maps to NM_015154.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr16:12875066 G>A maps to NM_018340.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr16:12875066 G>A maps to NM_018340.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr18:19997859 G>A did not map to a codon.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr18:19997859 G>A did not map to a codon.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr19:36029511 C>T maps to NM_014364.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr19:36029511 C>T maps to NM_014364.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr2:100916304 C>A maps to NM_198461.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr2:100916304 C>A maps to NM_198461.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr2:141092129 T>C did not map to a codon.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr2:141092129 T>C did not map to a codon.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr20:56138742 C>T maps to NM_002591.3 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr20:56138742 C>T maps to NM_002591.3 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr21:43711760 C>T maps to NM_004915.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr21:43711760 C>T maps to NM_004915.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr21:46320282 G>A maps to NM_000211.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr21:46320282 G>A maps to NM_000211.3 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr22:32239727 G>T maps to NM_001136029.1 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr22:32239727 G>T maps to NM_001136029.1 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr3:164700075 G>A maps to NM_001041.3 N1790N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr3:164700075 G>A maps to NM_001041.3 N1790N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr4:77305566 G>A maps to NM_001042784.1 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr4:77305566 G>A maps to NM_001042784.1 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr5:140682772 T>C maps to NM_031947.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr5:140682772 T>C maps to NM_031947.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr6:76751735 G>A maps to NM_001563.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr6:76751735 G>A maps to NM_001563.2 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr7:88963594 C>A maps to NM_181646.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr7:88963594 C>A maps to NM_181646.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr9:136230518 G>A maps to NM_033161.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr9:136230518 G>A maps to NM_033161.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr9:138415759 G>A maps to NM_002297.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-0742-01A-01W-0348-08 chr9:138415759 G>A maps to NM_002297.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr10:7771921 A>T maps to NM_002216.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr10:7771921 A>T maps to NM_002216.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr11:93844969 G>A maps to NM_001098672.1 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr11:93844969 G>A maps to NM_001098672.1 T1130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr16:72184632 C>T maps to NM_031293.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr16:72184632 C>T maps to NM_031293.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr17:59876468 G>A maps to NM_032043.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr17:59876468 G>A maps to NM_032043.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr2:85892914 G>A maps to NM_198843.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr2:85892914 G>A maps to NM_198843.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr3:132198096 G>A maps to NM_015268.3 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr3:132198096 G>A maps to NM_015268.3 R912R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr4:10080541 G>A maps to NM_017491.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr4:10080541 G>A maps to NM_017491.3 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr4:48621288 A>G did not map to a codon.
Sequencing variant TCGA-15-1444-01A-02D-1696-08 chr4:48621288 A>G did not map to a codon.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:37948875 C>T maps to NM_025079.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:37948875 C>T maps to NM_025079.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:55078367 G>T maps to NM_176782.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:55078367 G>T maps to NM_176782.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:152193138 G>A maps to NM_001009931.1 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:152193138 G>A maps to NM_001009931.1 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:209797263 G>A maps to NM_000228.2 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr1:209797263 G>A maps to NM_000228.2 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr11:2186969 G>A maps to NM_199292.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr11:2186969 G>A maps to NM_199292.2 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr12:51696869 C>T did not map to a codon.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr12:51696869 C>T did not map to a codon.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr12:95604180 T>C maps to NM_018351.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr12:95604180 T>C maps to NM_018351.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr15:81041940 C>T maps to NM_021214.1 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr15:81041940 C>T maps to NM_021214.1 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr15:85448819 A>T maps to NM_004213.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr15:85448819 A>T maps to NM_004213.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr16:70917862 G>A maps to NM_032821.2 A3312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr16:70917862 G>A maps to NM_032821.2 A3312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr17:12656062 G>A maps to NM_001146312.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr17:12656062 G>A maps to NM_001146312.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr18:7231553 C>T maps to NM_001105581.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr18:7231553 C>T maps to NM_001105581.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr18:61377522 G>A maps to NM_080475.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr18:61377522 G>A maps to NM_080475.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr19:10794067 A>G maps to NM_017620.2 Q571Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr19:10794067 A>G maps to NM_017620.2 Q571Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr19:50979618 G>A maps to ENST00000391816 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr19:50979618 G>A maps to ENST00000391816 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr2:219689034 C>T maps to NM_017431.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr2:219689034 C>T maps to NM_017431.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr22:37578305 G>A maps to NM_182486.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr22:37578305 G>A maps to NM_182486.1 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr22:38046221 G>A maps to NM_018957.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr22:38046221 G>A maps to NM_018957.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr4:174219325 C>T maps to NM_017423.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr4:174219325 C>T maps to NM_017423.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr6:24563627 C>T maps to NM_014809.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr6:24563627 C>T maps to NM_014809.3 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr7:29160575 T>C maps to NM_031311.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr7:29160575 T>C maps to NM_031311.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr7:103124179 G>A maps to ENST00000428762 N3367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr7:103124179 G>A maps to ENST00000428762 N3367N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr8:28627525 G>T maps to NM_018250.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr8:28627525 G>T maps to NM_018250.3 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr8:48772254 G>A maps to NM_006904.6 Q2041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr8:48772254 G>A maps to NM_006904.6 Q2041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr9:100433447 C>T maps to NM_002486.4 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chr9:100433447 C>T maps to NM_002486.4 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chrX:151124001 G>T maps to NM_004961.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0846-01A-01W-0424-08 chrX:151124001 G>T maps to NM_004961.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr1:152284951 C>A maps to NM_002016.1 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr1:152284951 C>A maps to NM_002016.1 E804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr1:158323686 C>T did not map to a codon.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr1:158323686 C>T did not map to a codon.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr11:107518219 T>A maps to NM_018712.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr11:107518219 T>A maps to NM_018712.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr12:15262108 G>A maps to NM_032918.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr12:15262108 G>A maps to NM_032918.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr12:79693292 G>T maps to NM_005639.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr12:79693292 G>T maps to NM_005639.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr12:118198970 C>T maps to ENST00000339824 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr12:118198970 C>T maps to ENST00000339824 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr14:25101152 G>A maps to ENST00000382542 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr14:25101152 G>A maps to ENST00000382542 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr14:91948147 A>G maps to ENST00000417249 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr14:91948147 A>G maps to ENST00000417249 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr15:63127964 C>T maps to NM_015059.2 D2386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr15:63127964 C>T maps to NM_015059.2 D2386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr15:91811769 C>T maps to NM_014848.4 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr15:91811769 C>T maps to NM_014848.4 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr16:28844549 A>T maps to NM_148414.1 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr16:28844549 A>T maps to NM_148414.1 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr16:57741547 G>A maps to NM_032269.5 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr16:57741547 G>A maps to NM_032269.5 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr18:6894891 T>C did not map to a codon.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr18:6894891 T>C did not map to a codon.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr18:28736014 G>A maps to NM_024421.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr18:28736014 G>A maps to NM_024421.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr19:3825267 C>T maps to NM_015174.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr19:3825267 C>T maps to NM_015174.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr2:132237805 C>T maps to NM_080386.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr2:132237805 C>T maps to NM_080386.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr2:160729002 A>G maps to NM_001198759.1 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr2:160729002 A>G maps to NM_001198759.1 D692D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr2:220159755 G>A maps to NM_002846.3 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr2:220159755 G>A maps to NM_002846.3 F872F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr3:38139019 T>C maps to NM_007335.2 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr3:38139019 T>C maps to NM_007335.2 F819F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr6:56342226 G>A maps to ENST00000361203 G6986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr6:56342226 G>A maps to ENST00000361203 G6986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr7:139416740 C>T maps to NM_022740.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chr7:139416740 C>T maps to NM_022740.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chrX:138864836 A>G maps to NM_173694.4 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-0861-01A-01W-0424-08 chrX:138864836 A>G maps to NM_173694.4 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:46972777 G>A maps to NM_147192.2 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:46972777 G>A maps to NM_147192.2 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:180063489 A>G maps to NM_014810.4 K2750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:180063489 A>G maps to NM_014810.4 K2750K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:186329080 T>C maps to NM_003292.2 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:186329080 T>C maps to NM_003292.2 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:238053167 T>A maps to NM_021186.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr1:238053167 T>A maps to NM_021186.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr10:89720851 C>T maps to NM_000314.4 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr10:105813705 T>C maps to NM_000494.3 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr10:105813705 T>C maps to NM_000494.3 Q602Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:4976145 G>A maps to NM_001004748.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:4976145 G>A maps to NM_001004748.1 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:5699637 G>A maps to NM_033034.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:5699637 G>A maps to NM_033034.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:58189828 C>A maps to NM_001005566.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:58189828 C>A maps to NM_001005566.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:113813843 G>T maps to NM_006028.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr11:113813843 G>T maps to NM_006028.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:21733299 G>A maps to NM_021957.3 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:21733299 G>A maps to NM_021957.3 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:131620611 G>C maps to NM_198827.3 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:131620611 G>C maps to NM_198827.3 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:133682984 A>G maps to NM_003440.2 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr12:133682984 A>G maps to NM_003440.2 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr15:68118858 C>T maps to ENST00000380035 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr15:68118858 C>T maps to ENST00000380035 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr17:34851064 A>G did not map to a codon.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr17:34851064 A>G did not map to a codon.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr17:60758248 G>A maps to NM_006039.3 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr17:60758248 G>A maps to NM_006039.3 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr18:22806840 G>A maps to NM_015461.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr18:22806840 G>A maps to NM_015461.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr19:12876794 G>A maps to NM_013312.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr19:12876794 G>A maps to NM_013312.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr19:38954118 C>T maps to NM_000540.2 H878H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr19:38954118 C>T maps to NM_000540.2 H878H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr19:56155984 C>T maps to NM_016535.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr19:56155984 C>T maps to NM_016535.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr2:74761512 G>A maps to NM_032603.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr2:74761512 G>A maps to NM_032603.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr2:225666722 G>A maps to NM_014689.2 Q1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr2:225666722 G>A maps to NM_014689.2 Q1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr2:241556393 C>T maps to ENST00000270364 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr2:241556393 C>T maps to ENST00000270364 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr20:36932753 C>T maps to NM_001725.2 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr20:36932753 C>T maps to NM_001725.2 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr20:48503377 C>T maps to ENST00000417961 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr20:48503377 C>T maps to ENST00000417961 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr21:40571509 G>T maps to NM_018963.3 S1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr21:40571509 G>T maps to NM_018963.3 S1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr22:24466764 G>A maps to NM_012295.3 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr22:24466764 G>A maps to NM_012295.3 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr3:3139897 T>C maps to NM_000564.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr3:3139897 T>C maps to NM_000564.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr3:168845828 G>A maps to NM_004991.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr3:168845828 G>A maps to NM_004991.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr4:69184553 C>A maps to NM_001031732.2 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr4:69184553 C>A maps to NM_001031732.2 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr4:141545489 C>T maps to NM_015130.2 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr4:141545489 C>T maps to NM_015130.2 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:2255802 G>A maps to NM_003550.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:2255802 G>A maps to NM_003550.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:36917678 C>T maps to NM_014800.9 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:36917678 C>T maps to NM_014800.9 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:81589045 C>T maps to NM_000722.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:81589045 C>T maps to NM_000722.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:94937423 A>T maps to NM_000446.5 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:94937423 A>T maps to NM_000446.5 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:100175847 G>A maps to NM_002319.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:100175847 G>A maps to NM_002319.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:100201640 C>T maps to NM_002593.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr7:100201640 C>T maps to NM_002593.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr8:19190496 A>G maps to NM_022071.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr8:19190496 A>G maps to NM_022071.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr9:2643640 C>T maps to NM_003383.3 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr9:2643640 C>T maps to NM_003383.3 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr9:95768390 C>T maps to NM_033086.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chr9:95768390 C>T maps to NM_033086.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:53612009 G>A maps to ENST00000276009 R1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:53612009 G>A maps to ENST00000276009 R1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:107939577 C>T maps to ENST00000328300 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:107939577 C>T maps to ENST00000328300 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:120181969 G>A maps to NM_012084.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:120181969 G>A maps to NM_012084.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:128887223 C>T maps to NM_003399.5 H369H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1045-01B-01W-0611-08 chrX:128887223 C>T maps to NM_003399.5 H369H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr1:1902132 G>A maps to ENST00000434971 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr1:1902132 G>A maps to ENST00000434971 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr1:53370461 C>T maps to ENST00000371522 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr1:53370461 C>T maps to ENST00000371522 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr1:158669788 G>A maps to NM_001005279.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr1:158669788 G>A maps to NM_001005279.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr10:118307870 G>A did not map to a codon.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr10:118307870 G>A did not map to a codon.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr10:118728201 G>T maps to NM_001127211.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr10:118728201 G>T maps to NM_001127211.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:65714722 C>T maps to NM_152762.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:65714722 C>T maps to NM_152762.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:75439861 C>T maps to NM_025098.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:75439861 C>T maps to NM_025098.2 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:76990355 G>A maps to ENST00000376217 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:76990355 G>A maps to ENST00000376217 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:94532994 G>A maps to NM_130847.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr11:94532994 G>A maps to NM_130847.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr12:50355943 G>A maps to NM_001651.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr12:50355943 G>A maps to NM_001651.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr12:57167872 G>A maps to NM_003725.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr12:57167872 G>A maps to NM_003725.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr12:117669898 C>T maps to ENST00000338101 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr12:117669898 C>T maps to ENST00000338101 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr15:30659650 G>A maps to NM_139320.1 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr15:30659650 G>A maps to NM_139320.1 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr16:2812073 G>A maps to NM_016333.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr16:2812073 G>A maps to NM_016333.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr17:7989532 G>T maps to NM_001139.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr17:7989532 G>T maps to NM_001139.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr17:58740520 G>T maps to NM_003620.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr17:58740520 G>T maps to NM_003620.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr17:72588367 T>G maps to NM_152460.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr17:72588367 T>G maps to NM_152460.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr18:2892200 G>A maps to NM_032048.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr18:2892200 G>A maps to NM_032048.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr18:56587376 G>T maps to NM_018181.4 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr18:56587376 G>T maps to NM_018181.4 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr2:182358130 G>A maps to NM_000885.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr2:182358130 G>A maps to NM_000885.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr2:242004745 G>A maps to NM_001080437.1 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr2:242004745 G>A maps to NM_001080437.1 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr21:46078018 G>A maps to NM_198697.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr21:46078018 G>A maps to NM_198697.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr4:110384777 G>A maps to NM_006323.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr4:110384777 G>A maps to NM_006323.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr5:131607723 C>G maps to NM_003687.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr5:131607723 C>G maps to NM_003687.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr6:91226311 C>A maps to NM_145331.1 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr6:91226311 C>A maps to NM_145331.1 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr7:7412800 T>C maps to NM_001037763.2 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr7:7412800 T>C maps to NM_001037763.2 K912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr7:100730793 C>T maps to NM_030961.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr7:100730793 C>T maps to NM_030961.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr8:24199149 G>A maps to NM_014265.4 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chr8:24199149 G>A maps to NM_014265.4 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chrX:53970578 C>T maps to NM_001184896.1 K915K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chrX:53970578 C>T maps to NM_001184896.1 K915K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chrX:54784129 G>A maps to NM_198510.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chrX:54784129 G>A maps to NM_198510.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chrY:4966470 A>G maps to NM_032973.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-16-1048-01B-01D-1353-08 chrY:4966470 A>G maps to NM_032973.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:43905597 G>A maps to NM_015284.2 G1464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:43905597 G>A maps to NM_015284.2 G1464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:57535098 C>T did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:57535098 C>T did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:76877751 C>T maps to NM_152996.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:76877751 C>T maps to NM_152996.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:163044109 G>A did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:163044109 G>A did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:170928686 T>G maps to NM_001163629.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:170928686 T>G maps to NM_001163629.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:207300202 T>C maps to NM_000715.3 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr1:207300202 T>C maps to NM_000715.3 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr10:47000007 G>A maps to NM_014696.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr10:47000007 G>A maps to NM_014696.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr10:117061474 C>T maps to NM_207303.2 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr10:117061474 C>T maps to NM_207303.2 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr11:866599 A>G maps to ENST00000409531 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr11:866599 A>G maps to ENST00000409531 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr11:55340232 C>T maps to NM_001004701.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr11:55340232 C>T maps to NM_001004701.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr11:58295178 A>G maps to NM_004811.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr11:58295178 A>G maps to NM_004811.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr12:41410533 A>T maps to NM_001843.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr12:41410533 A>T maps to NM_001843.2 A745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr12:70949683 C>T maps to NM_001109754.1 E1653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr12:70949683 C>T maps to NM_001109754.1 E1653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr13:61985657 T>C maps to NM_022843.3 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr13:61985657 T>C maps to NM_022843.3 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr13:109859099 T>C maps to NM_015011.1 P1831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr13:109859099 T>C maps to NM_015011.1 P1831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr15:42364080 G>A maps to NM_178034.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr15:42364080 G>A maps to NM_178034.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr15:50211035 C>A maps to NM_024837.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr15:50211035 C>A maps to NM_024837.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr16:30198719 C>T maps to NM_007074.3 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr16:30198719 C>T maps to NM_007074.3 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr16:31471306 C>T maps to ENST00000408912 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr16:31471306 C>T maps to ENST00000408912 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr17:37866666 G>A maps to NM_004448.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr17:37866666 G>A maps to NM_004448.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr18:29046571 C>T maps to NM_001944.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr18:29046571 C>T maps to NM_001944.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr19:8966764 C>T maps to NM_024690.2 S14396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr19:8966764 C>T maps to NM_024690.2 S14396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr19:35800999 C>T maps to NM_002361.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr19:35800999 C>T maps to NM_002361.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr19:49557639 G>A maps to ENST00000377280 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr19:49557639 G>A maps to ENST00000377280 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr2:29268217 T>A maps to NM_199280.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr2:29268217 T>A maps to NM_199280.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr2:73651878 T>A maps to NM_015120.4 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr2:73651878 T>A maps to NM_015120.4 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr2:217329390 G>A did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr2:217329390 G>A did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr3:46720750 G>A maps to NM_147129.3 D525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr3:46720750 G>A maps to NM_147129.3 D525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr3:108778662 C>A maps to NM_014429.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr3:108778662 C>A maps to NM_014429.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr3:122004022 C>T maps to NM_001178065.1 N1084N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr3:122004022 C>T maps to NM_001178065.1 N1084N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr4:79418092 C>A maps to NM_025074.6 I3031I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr4:79418092 C>A maps to NM_025074.6 I3031I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr4:156764949 G>A maps to NM_017419.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr4:156764949 G>A maps to NM_017419.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr4:162459447 A>G maps to NM_020116.3 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr4:162459447 A>G maps to NM_020116.3 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:2749778 G>A maps to NM_033267.4 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:2749778 G>A maps to NM_033267.4 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:78612054 T>C maps to NM_152405.4 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:78612054 T>C maps to NM_152405.4 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:112174281 T>C maps to NM_001127510.2 Y997Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:112174281 T>C maps to NM_001127510.2 Y997Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:179201676 C>T maps to NM_014757.4 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr5:179201676 C>T maps to NM_014757.4 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr6:12164549 T>C maps to NM_002114.2 V2671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr6:12164549 T>C maps to NM_002114.2 V2671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr7:53103789 G>A maps to NM_182595.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr7:53103789 G>A maps to NM_182595.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr7:115889256 T>A maps to NM_015641.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr7:115889256 T>A maps to NM_015641.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr8:62212805 T>C maps to NM_173519.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chr8:62212805 T>C maps to NM_173519.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:18690197 G>A did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:18690197 G>A did not map to a codon.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:39932303 G>A maps to NM_001123385.1 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:39932303 G>A maps to NM_001123385.1 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:50653944 C>T maps to NM_005448.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:50653944 C>T maps to NM_005448.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:128721073 A>G maps to NM_000276.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:128721073 A>G maps to NM_000276.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:153033711 C>T maps to NM_005393.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1390-01A-01D-1495-08 chrX:153033711 C>T maps to NM_005393.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:15978326 C>A maps to NM_032341.4 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:15978326 C>A maps to NM_032341.4 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:16330878 C>A maps to NM_178840.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:16330878 C>A maps to NM_178840.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:27099915 C>T maps to NM_006015.4 G1265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:27099915 C>T maps to NM_006015.4 G1265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:47498945 G>A maps to NM_178033.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:47498945 G>A maps to NM_178033.1 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:120510200 C>A maps to NM_024408.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:120510200 C>A maps to NM_024408.2 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:182922238 G>A maps to ENST00000287709 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr1:182922238 G>A maps to ENST00000287709 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr10:75407261 A>G maps to NM_001114133.1 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr10:75407261 A>G maps to NM_001114133.1 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr10:124358593 C>T maps to ENST00000368915 D1087D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr10:124358593 C>T maps to ENST00000368915 D1087D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr10:124390739 C>T maps to ENST00000368915 R2097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr10:124390739 C>T maps to ENST00000368915 R2097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:35313907 C>T maps to NM_004171.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:35313907 C>T maps to NM_004171.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:46321655 C>T maps to ENST00000288400 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:46321655 C>T maps to ENST00000288400 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:46916319 G>A maps to ENST00000256991 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:46916319 G>A maps to ENST00000256991 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:57798589 C>T maps to NM_001005186.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr11:57798589 C>T maps to NM_001005186.2 R56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr12:9251274 G>C maps to NM_000014.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr12:9251274 G>C maps to NM_000014.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr12:49416567 C>A maps to NM_003482.3 V5381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr12:49416567 C>A maps to NM_003482.3 V5381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr14:24886186 G>A maps to NM_025081.2 L1744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr14:24886186 G>A maps to NM_025081.2 L1744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr14:60749966 A>G maps to NM_177952.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr14:60749966 A>G maps to NM_177952.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr14:105409034 A>G maps to NM_138420.2 D4251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr14:105409034 A>G maps to NM_138420.2 D4251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr15:26866465 C>G maps to NM_021912.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr15:26866465 C>G maps to NM_021912.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr16:55907824 C>T maps to NM_001143685.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr16:55907824 C>T maps to NM_001143685.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:28968937 G>A maps to NM_001134453.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:28968937 G>A maps to NM_001134453.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:57105363 C>T maps to NM_133459.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:57105363 C>T maps to NM_133459.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:60033974 C>T maps to NM_003839.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:60033974 C>T maps to NM_003839.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:67718719 G>T maps to NM_173630.3 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr18:67718719 G>T maps to NM_173630.3 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:17844117 C>T maps to NM_018174.4 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:17844117 C>T maps to NM_018174.4 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:35512754 C>A maps to NM_020895.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:35512754 C>A maps to NM_020895.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:36673610 G>A maps to ENST00000355114 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:36673610 G>A maps to ENST00000355114 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:43689015 G>A maps to ENST00000270059 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:43689015 G>A maps to ENST00000270059 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:47197300 G>A maps to ENST00000449438 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:47197300 G>A maps to ENST00000449438 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:47879752 C>T maps to NM_014681.5 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:47879752 C>T maps to NM_014681.5 F845F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:55447702 G>A maps to ENST00000446217 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:55447702 G>A maps to ENST00000446217 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:58640192 G>A maps to NM_024620.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr19:58640192 G>A maps to NM_024620.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:27465507 G>T maps to NM_004341.3 L2081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:27465507 G>T maps to NM_004341.3 L2081L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:32710743 G>A maps to NM_016252.3 Q2577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:32710743 G>A maps to NM_016252.3 Q2577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:73316178 T>C maps to NM_015470.2 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:73316178 T>C maps to NM_015470.2 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:193049125 T>C maps to NM_016192.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:193049125 T>C maps to NM_016192.2 K122K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:241069333 C>T maps to NM_138336.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr2:241069333 C>T maps to NM_138336.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr20:409648 C>T maps to NM_031229.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr20:409648 C>T maps to NM_031229.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr3:135721606 G>T maps to NM_002718.4 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr3:135721606 G>T maps to NM_002718.4 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr3:141006222 G>T maps to NM_001037172.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr3:141006222 G>T maps to NM_001037172.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr3:195611778 G>C maps to NM_001010938.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr3:195611778 G>C maps to NM_001010938.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr4:1986589 G>A maps to NM_005663.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr4:1986589 G>A maps to NM_005663.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr4:20598279 T>A did not map to a codon.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr4:20598279 T>A did not map to a codon.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr4:169824984 C>A maps to NM_001166108.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr4:169824984 C>A maps to NM_001166108.1 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr5:37064645 A>G maps to NM_133433.3 K2689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr5:37064645 A>G maps to NM_133433.3 K2689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr5:39288824 C>A maps to NM_001737.3 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr5:39288824 C>A maps to NM_001737.3 G549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr5:154396907 C>A maps to NM_001099293.1 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr5:154396907 C>A maps to NM_001099293.1 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr7:100674924 C>T maps to NM_001040105.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr7:100674924 C>T maps to NM_001040105.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr7:113558409 A>C maps to NM_002711.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr7:113558409 A>C maps to NM_002711.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr8:41530098 G>A maps to ENST00000415018 D1623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr8:41530098 G>A maps to ENST00000415018 D1623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr8:110131344 G>A maps to NM_003301.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr8:110131344 G>A maps to NM_003301.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr8:146076336 C>T maps to NM_001081003.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chr8:146076336 C>T maps to NM_001081003.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:8433515 G>T maps to NM_001001888.3 G9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:8433515 G>T maps to NM_001001888.3 G9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:69250323 T>C maps to NM_001399.4 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:69250323 T>C maps to NM_001399.4 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:72674300 G>A maps to NM_005193.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:72674300 G>A maps to NM_005193.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:83128533 C>G maps to NM_021118.1 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-1790-01B-01D-1353-08 chrX:83128533 C>G maps to NM_021118.1 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:91843656 C>T maps to NM_001017975.3 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:91843656 C>T maps to NM_001017975.3 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:151774510 G>A maps to NM_001004432.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:151774510 G>A maps to NM_001004432.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:156011961 G>C maps to NM_020131.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:156011961 G>C maps to NM_020131.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:156834160 G>A maps to NM_002529.3 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:156834160 G>A maps to NM_002529.3 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:169489787 G>A maps to ENST00000367796 R2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:169489787 G>A maps to ENST00000367796 R2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:202287758 C>A maps to NM_001017403.1 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr1:202287758 C>A maps to NM_001017403.1 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr10:7762868 C>T maps to NM_002216.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr10:7762868 C>T maps to NM_002216.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr12:80014953 G>A maps to NM_002583.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr12:80014953 G>A maps to NM_002583.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr13:99042245 C>T maps to NM_005766.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr13:99042245 C>T maps to NM_005766.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr16:23570882 C>T maps to ENST00000219638 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr16:23570882 C>T maps to ENST00000219638 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr17:695047 G>A maps to NM_018146.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr17:695047 G>A maps to NM_018146.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr17:72915619 C>T maps to NM_173477.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr17:72915619 C>T maps to NM_173477.2 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr18:33060422 G>A maps to NM_001098817.1 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr18:33060422 G>A maps to NM_001098817.1 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr18:61310406 A>T maps to NM_002974.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr18:61310406 A>T maps to NM_002974.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr19:5587915 G>A maps to NM_014649.2 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr19:5587915 G>A maps to NM_014649.2 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr2:3193248 G>A maps to ENST00000398659 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr2:3193248 G>A maps to ENST00000398659 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr2:102486217 G>A maps to NM_145686.2 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr2:102486217 G>A maps to NM_145686.2 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr5:63257204 G>A maps to NM_000524.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr5:63257204 G>A maps to NM_000524.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr5:176794017 C>A maps to ENST00000398128 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr5:176794017 C>A maps to ENST00000398128 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr6:43109924 G>A maps to NM_002821.3 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr6:43109924 G>A maps to NM_002821.3 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr6:161127556 C>T maps to NM_000301.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr6:161127556 C>T maps to NM_000301.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr7:64168370 G>A maps to NM_016220.3 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr7:64168370 G>A maps to NM_016220.3 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr9:21077337 G>A maps to NM_002176.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chr9:21077337 G>A maps to NM_002176.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chrX:48751095 G>A maps to NM_001167947.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chrX:48751095 G>A maps to NM_001167947.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chrX:117722098 G>T did not map to a codon.
Sequencing variant TCGA-19-2619-01A-01D-1495-08 chrX:117722098 G>T did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:11562050 G>A maps to NM_020780.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:11562050 G>A maps to NM_020780.1 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:110086039 G>A maps to NM_031936.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:110086039 G>A maps to NM_031936.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:117618057 G>A maps to NM_003594.3 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:117618057 G>A maps to NM_003594.3 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:152283518 G>A maps to NM_002016.1 D1281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:152283518 G>A maps to NM_002016.1 D1281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:186050514 C>T maps to NM_031935.2 R2926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:186050514 C>T maps to NM_031935.2 R2926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:205280830 A>G did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr1:205280830 A>G did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr11:125542538 C>T maps to NM_001612.5 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr11:125542538 C>T maps to NM_001612.5 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:43833725 G>A maps to ENST00000389420 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:43833725 G>A maps to ENST00000389420 R813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:48723148 G>A maps to NM_181788.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:48723148 G>A maps to NM_181788.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:58022669 G>A maps to NM_001478.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:58022669 G>A maps to NM_001478.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:113629391 C>T maps to NM_032848.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr12:113629391 C>T maps to NM_032848.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr14:105859120 C>G maps to ENST00000458164 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr14:105859120 C>G maps to ENST00000458164 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr16:20328645 G>T maps to NM_001007240.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr16:20328645 G>T maps to NM_001007240.1 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr16:21053360 G>A maps to NM_017539.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr16:21053360 G>A maps to NM_017539.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr17:29508438 G>A did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr17:29508438 G>A did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr18:21043043 G>A did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr18:21043043 G>A did not map to a codon.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr19:14952341 G>A maps to NM_001005190.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr19:14952341 G>A maps to NM_001005190.1 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr2:170066148 G>A maps to NM_004525.2 R2095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr2:170066148 G>A maps to NM_004525.2 R2095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr2:201881770 G>A maps to NM_173822.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr2:201881770 G>A maps to NM_173822.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr2:234835205 C>A maps to NM_024080.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr2:234835205 C>A maps to NM_024080.4 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr20:61907549 C>A maps to NM_175609.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr20:61907549 C>A maps to NM_175609.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr4:77288529 G>A maps to NM_001042784.1 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr4:77288529 G>A maps to NM_001042784.1 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr4:138451922 C>T maps to NM_019035.3 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr4:138451922 C>T maps to NM_019035.3 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr5:140188685 C>T maps to NM_018907.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr5:140188685 C>T maps to NM_018907.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr5:154188109 G>A maps to ENST00000377643 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr5:154188109 G>A maps to ENST00000377643 K930K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr6:139183818 G>A maps to NM_001195037.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr6:139183818 G>A maps to NM_001195037.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr7:44579248 G>A maps to NM_013389.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr7:44579248 G>A maps to NM_013389.2 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr9:139306463 G>A maps to NM_015160.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chr9:139306463 G>A maps to NM_015160.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chrX:117043735 C>T maps to NM_033495.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2620-01A-01D-1495-08 chrX:117043735 C>T maps to NM_033495.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:19992746 C>T maps to NM_000871.1 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:19992746 C>T maps to NM_000871.1 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:33402781 C>T maps to NM_153341.2 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:33402781 C>T maps to NM_153341.2 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:40770006 G>A maps to NM_001852.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:40770006 G>A maps to NM_001852.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:78958622 G>A maps to NM_000959.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:78958622 G>A maps to NM_000959.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:89650936 T>A maps to NM_052941.4 *641Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:89650936 T>A maps to NM_052941.4 *641Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:116670944 G>A maps to NM_152367.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:116670944 G>A maps to NM_152367.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:144823889 C>G maps to NM_001037675.2 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:144823889 C>G maps to NM_001037675.2 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:160064842 G>A maps to NM_052868.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:160064842 G>A maps to NM_052868.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:177927422 G>A maps to NM_033127.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr1:177927422 G>A maps to NM_033127.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr11:55606712 G>A maps to NM_001005496.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr11:55606712 G>A maps to NM_001005496.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr11:119535606 G>C maps to NM_002855.4 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr11:119535606 G>C maps to NM_002855.4 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr12:21681995 G>A maps to NM_030572.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr12:21681995 G>A maps to NM_030572.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr12:26628303 A>G maps to NM_002223.2 H2089H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr12:26628303 A>G maps to NM_002223.2 H2089H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr14:105477699 G>A maps to NM_145701.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr14:105477699 G>A maps to NM_145701.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr15:23812071 G>A maps to NM_005664.3 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr15:23812071 G>A maps to NM_005664.3 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr15:40093623 C>T maps to NM_007223.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr15:40093623 C>T maps to NM_007223.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr15:45724276 C>T maps to NM_197955.1 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr15:45724276 C>T maps to NM_197955.1 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr16:15857676 G>A maps to NM_001040114.1 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr16:15857676 G>A maps to NM_001040114.1 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr16:31426281 C>T maps to ENST00000444228 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr16:31426281 C>T maps to ENST00000444228 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr17:38911513 G>A maps to NM_181534.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr17:38911513 G>A maps to NM_181534.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr18:43668120 T>C maps to NM_001001937.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr18:43668120 T>C maps to NM_001001937.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr19:8160956 G>A maps to NM_032447.3 D1849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr19:8160956 G>A maps to NM_032447.3 D1849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr19:39908256 T>C maps to NM_022835.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr19:39908256 T>C maps to NM_022835.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr19:55501995 G>C maps to NM_017852.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr19:55501995 G>C maps to NM_017852.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:152470899 G>A maps to NM_001164507.1 Q3831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:152470899 G>A maps to NM_001164507.1 Q3831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:185801477 C>G maps to NM_194250.1 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:185801477 C>G maps to NM_194250.1 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:189851837 A>G maps to NM_000090.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:189851837 A>G maps to NM_000090.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:234891860 C>T maps to NM_024080.4 D918D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr2:234891860 C>T maps to NM_024080.4 D918D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr20:57767831 C>T maps to NM_178457.1 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr20:57767831 C>T maps to NM_178457.1 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr3:12858461 C>T maps to NM_001162499.1 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr3:12858461 C>T maps to NM_001162499.1 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr3:38748875 T>C did not map to a codon.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr3:38748875 T>C did not map to a codon.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr4:74847162 G>A maps to NM_002619.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr4:74847162 G>A maps to NM_002619.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr5:41012777 G>A maps to ENST00000296803 D1015D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr5:41012777 G>A maps to ENST00000296803 D1015D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr5:136476317 G>A maps to NM_004598.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr5:136476317 G>A maps to NM_004598.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr6:44268961 G>C maps to NM_020745.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr6:44268961 G>C maps to NM_020745.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr6:63991035 G>T maps to NM_016571.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr6:63991035 G>T maps to NM_016571.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr6:160679390 C>T maps to NM_003058.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr6:160679390 C>T maps to NM_003058.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr8:49643174 A>G maps to NM_024593.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr8:49643174 A>G maps to NM_024593.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr8:120118081 C>T maps to NM_006438.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr8:120118081 C>T maps to NM_006438.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr8:143956450 G>A maps to ENST00000377675 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr8:143956450 G>A maps to ENST00000377675 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr9:139092591 C>T maps to NM_014564.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2623-01A-01D-1495-08 chr9:139092591 C>T maps to NM_014564.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:1636295 C>T did not map to a codon.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:1636295 C>T did not map to a codon.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:2461381 C>G maps to NM_001010926.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:2461381 C>G maps to NM_001010926.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:203818960 G>A maps to NM_014827.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:203818960 G>A maps to NM_014827.4 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:243362437 A>G maps to NM_014812.2 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr1:243362437 A>G maps to NM_014812.2 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr10:97396855 A>T maps to NM_002860.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr10:97396855 A>T maps to NM_002860.3 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr10:135084466 G>A maps to NM_001109.4 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr10:135084466 G>A maps to NM_001109.4 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr11:558884 G>A maps to NM_173573.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr11:558884 G>A maps to NM_173573.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr12:53662941 G>A maps to NM_012291.4 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr12:53662941 G>A maps to NM_012291.4 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr12:97345746 G>A maps to NM_001135175.1 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr12:97345746 G>A maps to NM_001135175.1 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr12:111895055 G>A maps to NM_002973.3 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr12:111895055 G>A maps to NM_002973.3 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr14:105418388 G>A maps to NM_138420.2 V1133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr14:105418388 G>A maps to NM_138420.2 V1133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr15:22332432 G>A did not map to a codon.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr15:22332432 G>A did not map to a codon.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr2:179442792 G>A maps to NM_133378.4 R20249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr2:179442792 G>A maps to NM_133378.4 R20249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr2:205986431 T>C maps to ENST00000406610 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr2:205986431 T>C maps to ENST00000406610 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr5:169508957 G>A maps to NM_004946.2 R1800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr5:169508957 G>A maps to NM_004946.2 R1800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr6:133005539 G>A maps to NM_004666.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr6:133005539 G>A maps to NM_004666.2 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr7:5959508 C>T maps to NM_015622.5 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr7:5959508 C>T maps to NM_015622.5 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr9:124538503 C>T maps to ENST00000408936 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2624-01A-01D-1495-08 chr9:124538503 C>T maps to ENST00000408936 R1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr11:118184558 C>T maps to NM_000733.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr11:118184558 C>T maps to NM_000733.3 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr12:49361973 G>T maps to NM_003394.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr12:49361973 G>T maps to NM_003394.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr14:75149997 C>T did not map to a codon.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr14:75149997 C>T did not map to a codon.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr16:72153834 G>A maps to NM_031293.2 C974C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr16:72153834 G>A maps to NM_031293.2 C974C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr16:75669878 C>T maps to NM_001130089.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr16:75669878 C>T maps to NM_001130089.1 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr19:11224246 T>C maps to NM_000527.4 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr19:11224246 T>C maps to NM_000527.4 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr2:234669016 G>A maps to NM_000463.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr2:234669016 G>A maps to NM_000463.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr20:44184400 G>A maps to NM_130896.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr20:44184400 G>A maps to NM_130896.2 C128C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr21:47546137 C>T maps to NM_001849.3 D803D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr21:47546137 C>T maps to NM_001849.3 D803D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr3:66455659 C>T maps to NM_015541.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr3:66455659 C>T maps to NM_015541.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr4:183710310 C>T maps to NM_001080477.1 D1790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr4:183710310 C>T maps to NM_001080477.1 D1790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr5:1085432 C>T maps to NM_006598.2 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr5:1085432 C>T maps to NM_006598.2 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr8:25232154 C>T maps to NM_024940.6 H1267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chr8:25232154 C>T maps to NM_024940.6 H1267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chrX:10096086 G>A maps to NM_015691.3 W722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2625-01A-01D-1495-08 chrX:10096086 G>A maps to NM_015691.3 W722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr1:86822222 C>T maps to ENST00000370567 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr1:86822222 C>T maps to ENST00000370567 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr1:155989852 C>A maps to ENST00000368312 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr1:155989852 C>A maps to ENST00000368312 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr1:161182255 C>T maps to NM_004550.4 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr1:161182255 C>T maps to NM_004550.4 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr11:7950019 G>A maps to NM_001004461.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr11:7950019 G>A maps to NM_001004461.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr12:14923760 A>G maps to NM_175054.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr12:14923760 A>G maps to NM_175054.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr13:39425865 A>G maps to NM_207361.4 E2262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr13:39425865 A>G maps to NM_207361.4 E2262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr16:56901058 C>T maps to NM_000339.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr16:56901058 C>T maps to NM_000339.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:10395867 G>T maps to NM_005963.3 V1895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:10395867 G>T maps to NM_005963.3 V1895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:18906957 G>A maps to NM_001039999.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:18906957 G>A maps to NM_001039999.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:78185891 G>A maps to NM_000199.3 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr17:78185891 G>A maps to NM_000199.3 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr2:219521104 C>T maps to NM_001105537.1 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr2:219521104 C>T maps to NM_001105537.1 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr21:45971182 C>G maps to NM_198693.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr21:45971182 C>G maps to NM_198693.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr22:31137201 G>A maps to NM_030758.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr22:31137201 G>A maps to NM_030758.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr3:13432742 C>T maps to NM_024923.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr3:13432742 C>T maps to NM_024923.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr3:126138548 G>A maps to ENST00000505024 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr3:126138548 G>A maps to ENST00000505024 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr3:189607255 A>G maps to NM_003722.4 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr3:189607255 A>G maps to NM_003722.4 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr4:69798343 A>G did not map to a codon.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr4:69798343 A>G did not map to a codon.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr4:187003772 G>A maps to NM_003265.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr4:187003772 G>A maps to NM_003265.2 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr6:101110218 A>T did not map to a codon.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr6:101110218 A>T did not map to a codon.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr7:31617702 G>A maps to NM_194300.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr7:31617702 G>A maps to NM_194300.2 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:22106019 C>T maps to NM_001722.2 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:22106019 C>T maps to NM_001722.2 N171N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:25287393 G>A maps to NM_017634.3 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:25287393 G>A maps to NM_017634.3 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:71069276 A>G maps to NM_006540.2 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:71069276 A>G maps to NM_006540.2 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:102705055 T>C maps to NM_032041.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr8:102705055 T>C maps to NM_032041.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr9:71687594 G>T maps to NM_000144.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr9:71687594 G>T maps to NM_000144.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr9:82227599 C>T maps to ENST00000376537 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr9:82227599 C>T maps to ENST00000376537 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr9:132585087 C>T maps to ENST00000437532 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2629-01A-01D-1495-08 chr9:132585087 C>T maps to ENST00000437532 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr1:159897139 G>A maps to NM_001135050.1 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr1:159897139 G>A maps to NM_001135050.1 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr10:27324682 T>C did not map to a codon.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr10:27324682 T>C did not map to a codon.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr11:6291992 C>T maps to NM_176875.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr11:6291992 C>T maps to NM_176875.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr11:67225876 G>A maps to NM_145200.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr11:67225876 G>A maps to NM_145200.3 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:11506565 C>T maps to NM_005039.3 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:11506565 C>T maps to NM_005039.3 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:52828034 G>A maps to ENST00000252245 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:52828034 G>A maps to ENST00000252245 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:62148676 G>A maps to NM_178539.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:62148676 G>A maps to NM_178539.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:123687853 G>A maps to NM_022782.2 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr12:123687853 G>A maps to NM_022782.2 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr14:24730964 A>G maps to NM_000359.2 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr14:24730964 A>G maps to NM_000359.2 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr15:26825567 G>A maps to NM_021912.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr15:26825567 G>A maps to NM_021912.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr16:20359593 C>T maps to ENST00000424589 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr16:20359593 C>T maps to ENST00000424589 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr17:18055237 C>T maps to ENST00000205890 T2622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr17:18055237 C>T maps to ENST00000205890 T2622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr17:21319067 C>T maps to NM_021012.4 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr17:21319067 C>T maps to NM_021012.4 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr19:8997531 G>A maps to NM_024690.2 A13630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr19:8997531 G>A maps to NM_024690.2 A13630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr20:39986527 G>T maps to NM_022896.1 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr20:39986527 G>T maps to NM_022896.1 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr20:50007935 C>T maps to NM_173091.2 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr20:50007935 C>T maps to NM_173091.2 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr3:58141765 C>T maps to NM_001164317.1 S2315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr3:58141765 C>T maps to NM_001164317.1 S2315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr3:138216905 G>A maps to NM_024491.2 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr3:138216905 G>A maps to NM_024491.2 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr5:35659270 C>T maps to NM_024867.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr5:35659270 C>T maps to NM_024867.3 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr5:43040064 C>T maps to NM_001014279.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr5:43040064 C>T maps to NM_001014279.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr5:140553180 C>T maps to NM_018940.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr5:140553180 C>T maps to NM_018940.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr7:126173578 G>A maps to NM_001127323.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr7:126173578 G>A maps to NM_001127323.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr7:134618734 A>G maps to NM_033138.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr7:134618734 A>G maps to NM_033138.3 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr9:84200543 G>A maps to NM_005077.3 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr9:84200543 G>A maps to NM_005077.3 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr9:97081001 G>T maps to NM_017561.1 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chr9:97081001 G>T maps to NM_017561.1 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chrX:140985022 T>C maps to NM_138702.1 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-2631-01A-01D-1353-08 chrX:140985022 T>C maps to NM_138702.1 Y493Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr1:185958747 C>T maps to NM_031935.2 Y1059Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr1:185958747 C>T maps to NM_031935.2 Y1059Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr10:26463062 C>T maps to NM_017433.4 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr10:26463062 C>T maps to NM_017433.4 S1290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr10:63170244 C>T maps to NM_178505.6 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr10:63170244 C>T maps to NM_178505.6 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:5529359 G>A maps to NM_017481.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:5529359 G>A maps to NM_017481.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:6646054 G>A maps to NM_003737.2 S2397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:6646054 G>A maps to NM_003737.2 S2397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:55587398 C>T maps to ENST00000395203 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:55587398 C>T maps to ENST00000395203 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:103006523 C>T maps to NM_001080463.1 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr11:103006523 C>T maps to NM_001080463.1 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr12:7519880 C>T maps to ENST00000416109 E1420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr12:7519880 C>T maps to ENST00000416109 E1420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr12:109693957 G>A maps to NM_001093.3 T2060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr12:109693957 G>A maps to NM_001093.3 T2060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr12:123473300 T>C maps to NM_020845.2 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr12:123473300 T>C maps to NM_020845.2 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr15:50209192 G>A maps to NM_024837.2 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr15:50209192 G>A maps to NM_024837.2 D693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr15:84257441 C>T maps to ENST00000434347 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr15:84257441 C>T maps to ENST00000434347 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr17:19642826 G>A maps to NM_000691.4 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr17:19642826 G>A maps to NM_000691.4 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr17:72283177 C>T maps to NM_023036.4 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr17:72283177 C>T maps to NM_023036.4 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr18:28986154 A>G maps to NM_001134453.1 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr18:28986154 A>G maps to NM_001134453.1 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr19:9072931 G>A maps to NM_024690.2 T4838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr19:9072931 G>A maps to NM_024690.2 T4838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr2:116548903 C>T maps to NM_020868.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr2:116548903 C>T maps to NM_020868.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr20:39726940 G>A maps to NM_003286.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr20:39726940 G>A maps to NM_003286.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:48510544 G>A maps to NM_016479.3 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:48510544 G>A maps to NM_016479.3 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:52156394 C>T maps to NM_015426.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:52156394 C>T maps to NM_015426.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:97124119 T>A did not map to a codon.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:97124119 T>A did not map to a codon.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:126708341 C>T maps to NM_032242.3 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr3:126708341 C>T maps to NM_032242.3 C302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr5:163558 G>A maps to NM_052909.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr5:163558 G>A maps to NM_052909.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr5:68647986 G>T maps to NM_016283.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr5:68647986 G>T maps to NM_016283.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr5:145435651 G>A maps to NM_152550.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr5:145435651 G>A maps to NM_152550.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr6:52141939 G>A maps to ENST00000419835 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr6:52141939 G>A maps to ENST00000419835 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr7:107600244 G>A maps to NM_002291.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr7:107600244 G>A maps to NM_002291.2 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:28385047 G>A maps to NM_017412.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:28385047 G>A maps to NM_017412.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:73993341 G>A maps to NM_153225.3 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:73993341 G>A maps to NM_153225.3 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:100874086 C>A maps to NM_017890.3 R3735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:100874086 C>A maps to NM_017890.3 R3735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:110463210 A>T maps to ENST00000426474 G2061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr8:110463210 A>T maps to ENST00000426474 G2061G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr9:84609452 C>A maps to NM_001001670.2 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr9:84609452 C>A maps to NM_001001670.2 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr9:130653178 C>A maps to NM_013443.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chr9:130653178 C>A maps to NM_013443.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chrX:70466242 G>T maps to ENST00000373988 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chrX:70466242 G>T maps to ENST00000373988 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chrX:129339340 G>A maps to NM_017666.4 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chrX:129339340 G>A maps to NM_017666.4 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chrX:138643869 G>A maps to NM_000133.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-4068-01A-01D-1353-08 chrX:138643869 G>A maps to NM_000133.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chr1:76288093 G>A maps to NM_002440.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chr1:76288093 G>A maps to NM_002440.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chr11:124623727 A>C maps to NM_138961.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chr11:124623727 A>C maps to NM_138961.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chr5:140209538 G>A maps to NM_018909.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chr5:140209538 G>A maps to NM_018909.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chrX:139038183 T>C maps to NM_001013403.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chrX:139038183 T>C maps to NM_001013403.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chrX:142967294 C>T maps to NM_001012989.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5947-01A-11D-1696-08 chrX:142967294 C>T maps to NM_001012989.1 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr1:32828322 C>A maps to NM_052841.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr1:32828322 C>A maps to NM_052841.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr10:7763616 C>T maps to NM_002216.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr10:7763616 C>T maps to NM_002216.2 H248H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr12:75601220 G>A maps to NM_139137.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr12:75601220 G>A maps to NM_139137.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr14:38061514 G>A maps to NM_004496.2 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr14:38061514 G>A maps to NM_004496.2 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr14:75388195 C>A maps to NM_031464.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr14:75388195 C>A maps to NM_031464.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr15:101567474 C>T maps to NM_024652.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr15:101567474 C>T maps to NM_024652.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr17:76557879 G>A maps to ENST00000389840 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr17:76557879 G>A maps to ENST00000389840 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr20:5903377 C>T maps to NM_001819.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr20:5903377 C>T maps to NM_001819.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr21:32253365 G>A maps to NM_175858.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr21:32253365 G>A maps to NM_175858.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr3:19574894 A>G maps to NM_144633.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr3:19574894 A>G maps to NM_144633.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr5:49698153 C>T did not map to a codon.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr5:49698153 C>T did not map to a codon.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr6:83841948 C>T maps to NM_015018.2 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr6:83841948 C>T maps to NM_015018.2 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr8:110424604 C>T maps to ENST00000426474 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr8:110424604 C>T maps to ENST00000426474 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr9:27455215 C>T maps to NM_024761.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr9:27455215 C>T maps to NM_024761.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr9:97329590 C>T maps to NM_003837.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chr9:97329590 C>T maps to NM_003837.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chrX:2873478 C>T maps to NM_000047.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chrX:2873478 C>T maps to NM_000047.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chrX:96139917 C>T maps to NM_013347.4 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5950-01A-11D-1696-08 chrX:96139917 C>T maps to NM_013347.4 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr1:186045740 A>G maps to NM_031935.2 V2824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr1:186045740 A>G maps to NM_031935.2 V2824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:60184369 T>C maps to NM_032597.3 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:60184369 T>C maps to NM_032597.3 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:66411464 C>T maps to NM_001198845.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:66411464 C>T maps to NM_001198845.1 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:119215662 G>A maps to NM_031433.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:119215662 G>A maps to NM_031433.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:123909126 G>A maps to NM_001004463.1 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr11:123909126 G>A maps to NM_001004463.1 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr12:49218454 A>G maps to NM_000725.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr12:49218454 A>G maps to NM_000725.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr13:61985633 C>T maps to NM_022843.3 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr13:61985633 C>T maps to NM_022843.3 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr14:20586155 G>A maps to NM_001004715.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr14:20586155 G>A maps to NM_001004715.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr16:31500622 G>A maps to ENST00000431354 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr16:31500622 G>A maps to ENST00000431354 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr16:67208818 C>T maps to ENST00000432069 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr16:67208818 C>T maps to ENST00000432069 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr19:6906477 C>T maps to ENST00000381407 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr19:6906477 C>T maps to ENST00000381407 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr19:10434233 G>A maps to NM_133452.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr19:10434233 G>A maps to NM_133452.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr19:43441293 C>T did not map to a codon.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr19:43441293 C>T did not map to a codon.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr2:160993972 G>A maps to NM_000888.3 C544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr2:160993972 G>A maps to NM_000888.3 C544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr20:17929611 C>T maps to NM_152227.1 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr20:17929611 C>T maps to NM_152227.1 E280E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr20:46264905 C>T maps to NM_181659.2 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr20:46264905 C>T maps to NM_181659.2 H592H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr21:41455892 C>T maps to NM_001389.3 T1391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr21:41455892 C>T maps to NM_001389.3 T1391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr3:52475288 G>A maps to NM_020163.1 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr3:52475288 G>A maps to NM_020163.1 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:4411319 C>T maps to NM_001040101.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:4411319 C>T maps to NM_001040101.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:110864420 T>C maps to NM_001963.4 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:110864420 T>C maps to NM_001963.4 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:143159104 G>A maps to NM_003866.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:143159104 G>A maps to NM_003866.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:170043336 A>G maps to NM_020870.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr4:170043336 A>G maps to NM_020870.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr6:5999376 C>T maps to NM_016588.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr6:5999376 C>T maps to NM_016588.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr7:143632552 C>T maps to NM_001004685.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr7:143632552 C>T maps to NM_001004685.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr8:25246734 G>A maps to NM_024940.6 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr8:25246734 G>A maps to NM_024940.6 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr9:34257896 G>A maps to NM_194313.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chr9:34257896 G>A maps to NM_194313.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chrX:2931163 G>A maps to NM_001011719.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chrX:2931163 G>A maps to NM_001011719.1 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chrX:47842805 T>C maps to NM_006962.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chrX:47842805 T>C maps to NM_006962.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chrX:119410874 G>T maps to NM_017938.3 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5951-01A-11D-1696-08 chrX:119410874 G>T maps to NM_017938.3 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr11:72114087 G>C maps to NM_030813.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr11:72114087 G>C maps to NM_030813.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr14:24787904 G>A maps to NM_139247.3 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr14:24787904 G>A maps to NM_139247.3 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr14:94849556 C>T maps to NM_001127707.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr14:94849556 C>T maps to NM_001127707.1 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr15:34064163 C>T maps to NM_001036.3 R2954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr15:34064163 C>T maps to NM_001036.3 R2954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr17:61271349 A>G did not map to a codon.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr17:61271349 A>G did not map to a codon.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr19:36293095 G>A maps to NM_021232.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr19:36293095 G>A maps to NM_021232.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr19:43439730 G>A maps to NM_002783.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr19:43439730 G>A maps to NM_002783.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr19:45153192 C>T maps to NM_006505.3 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr19:45153192 C>T maps to NM_006505.3 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr2:128408656 C>T maps to NM_005291.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr2:128408656 C>T maps to NM_005291.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr2:179548795 C>T maps to NM_133378.4 P9668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr2:179548795 C>T maps to NM_133378.4 P9668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr20:61297840 C>T maps to NM_016354.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr20:61297840 C>T maps to NM_016354.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr3:39307958 G>A maps to NM_001171174.1 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr3:39307958 G>A maps to NM_001171174.1 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr3:158378682 C>T maps to ENST00000264263 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr3:158378682 C>T maps to ENST00000264263 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr5:1880902 G>A maps to NM_016358.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr5:1880902 G>A maps to NM_016358.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr5:140754769 C>T maps to NM_018919.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr5:140754769 C>T maps to NM_018919.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr5:147807295 C>T maps to NM_205836.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr5:147807295 C>T maps to NM_205836.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr7:138593735 C>A did not map to a codon.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr7:138593735 C>A did not map to a codon.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr9:85913682 C>T maps to NM_174938.4 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5952-01A-11D-1696-08 chr9:85913682 C>T maps to NM_174938.4 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:17708558 G>A maps to NM_207421.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:17708558 G>A maps to NM_207421.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:21071370 A>G maps to NM_016287.3 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:21071370 A>G maps to NM_016287.3 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:32050586 C>T maps to NM_022164.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:32050586 C>T maps to NM_022164.2 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:91182596 A>G maps to NM_020063.1 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:91182596 A>G maps to NM_020063.1 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:120056673 C>T maps to ENST00000235547 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:120056673 C>T maps to ENST00000235547 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:144859987 C>G maps to NM_014644.4 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:144859987 C>G maps to NM_014644.4 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:161518334 G>A maps to NM_000569.6 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:161518334 G>A maps to NM_000569.6 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:180914468 C>T maps to NM_020950.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:180914468 C>T maps to NM_020950.1 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:209796521 G>T maps to NM_000228.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr1:209796521 G>T maps to NM_000228.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr11:56020020 C>T maps to NM_001004747.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr11:56020020 C>T maps to NM_001004747.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr11:70319234 C>T maps to ENST00000338508 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr11:70319234 C>T maps to ENST00000338508 S1757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr12:7842974 G>A maps to NM_020634.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr12:7842974 G>A maps to NM_020634.1 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr14:21469492 C>T maps to NM_014579.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr14:21469492 C>T maps to NM_014579.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr15:78922160 G>A maps to NM_000750.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr15:78922160 G>A maps to NM_000750.3 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr16:31435263 C>T maps to ENST00000444228 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr16:31435263 C>T maps to ENST00000444228 F1064F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr17:29588750 C>T maps to NM_001042492.2 R1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr17:29588750 C>T maps to NM_001042492.2 R1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr17:79412125 C>T maps to ENST00000436173 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr17:79412125 C>T maps to ENST00000436173 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr3:127981027 C>T maps to NM_021937.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr3:127981027 C>T maps to NM_021937.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr5:140725075 C>T maps to NM_018916.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr5:140725075 C>T maps to NM_018916.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr5:154135676 C>T maps to ENST00000377643 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr5:154135676 C>T maps to ENST00000377643 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr6:96054013 G>A maps to NM_024641.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr6:96054013 G>A maps to NM_024641.2 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr6:139266736 C>T maps to ENST00000367663 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr6:139266736 C>T maps to ENST00000367663 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr7:99753439 G>A maps to NM_018275.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr7:99753439 G>A maps to NM_018275.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr7:99998738 C>T maps to NM_017984.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr7:99998738 C>T maps to NM_017984.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr7:143772170 C>T maps to NM_001004488.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr7:143772170 C>T maps to NM_001004488.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr8:121021281 G>A maps to NM_022783.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr8:121021281 G>A maps to NM_022783.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr9:125909181 T>C maps to NM_018387.4 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5953-01B-12D-1845-08 chr9:125909181 T>C maps to NM_018387.4 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr1:1961507 C>T maps to NM_000815.4 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr1:1961507 C>T maps to NM_000815.4 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr10:129906301 G>A maps to NM_002417.4 R1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr10:129906301 G>A maps to NM_002417.4 R1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr11:58919917 A>G maps to NM_198847.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr11:58919917 A>G maps to NM_198847.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr11:117860219 C>T maps to NM_001558.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr11:117860219 C>T maps to NM_001558.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr12:53516998 A>G maps to NM_003578.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr12:53516998 A>G maps to NM_003578.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr14:75078641 C>T maps to NM_000428.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr14:75078641 C>T maps to NM_000428.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr15:58306464 G>A maps to NM_003888.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr15:58306464 G>A maps to NM_003888.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr16:1962052 G>A maps to ENST00000454677 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr16:1962052 G>A maps to ENST00000454677 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr18:61570322 G>A maps to NM_001143818.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr18:61570322 G>A maps to NM_001143818.1 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr2:132238150 C>T maps to NM_080386.2 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr2:132238150 C>T maps to NM_080386.2 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr2:201478598 G>A maps to NM_001159.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr2:201478598 G>A maps to NM_001159.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr21:46689871 G>A maps to NM_133635.4 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr21:46689871 G>A maps to NM_133635.4 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:32915462 C>T maps to NM_001039111.1 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:32915462 C>T maps to NM_001039111.1 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:97686290 G>T maps to NM_153182.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:97686290 G>T maps to NM_153182.2 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:105238917 A>T maps to NM_001627.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:105238917 A>T maps to NM_001627.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:178916622 C>T maps to NM_006218.2 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr3:178916622 C>T maps to NM_006218.2 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr4:10099514 C>T maps to NM_017491.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr4:10099514 C>T maps to NM_017491.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr5:90049614 G>A maps to NM_032119.3 A3782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr5:90049614 G>A maps to NM_032119.3 A3782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:84056026 A>G maps to NM_002395.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:84056026 A>G maps to NM_002395.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:100062502 C>T maps to ENST00000359773 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:100062502 C>T maps to ENST00000359773 D674D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:116720359 G>A did not map to a codon.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:116720359 G>A did not map to a codon.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:121427227 T>A maps to ENST00000275159 K1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr6:121427227 T>A maps to ENST00000275159 K1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr7:17861197 C>T maps to ENST00000417048 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr7:17861197 C>T maps to ENST00000417048 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr7:92761183 T>C maps to NM_152703.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr7:92761183 T>C maps to NM_152703.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr8:39836612 A>T maps to NM_194294.2 K88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr8:39836612 A>T maps to NM_194294.2 K88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr8:101149804 T>C maps to NM_001029860.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chr8:101149804 T>C maps to NM_001029860.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chrX:3242354 G>T maps to NM_015419.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chrX:3242354 G>T maps to NM_015419.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chrX:27999352 C>T maps to NM_001017930.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chrX:27999352 C>T maps to NM_001017930.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chrX:152915702 G>A maps to NM_001395.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5954-01A-11D-1696-08 chrX:152915702 G>A maps to NM_001395.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:11897138 C>T maps to ENST00000376496 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:11897138 C>T maps to ENST00000376496 N688N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:24202117 C>A did not map to a codon.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:24202117 C>A did not map to a codon.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:70716404 G>T maps to NM_004768.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:70716404 G>T maps to NM_004768.3 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:109270577 G>A maps to NM_001144937.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:109270577 G>A maps to NM_001144937.1 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:163306613 G>A maps to NM_145697.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:163306613 G>A maps to NM_145697.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:176734852 T>C maps to NM_020318.2 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:176734852 T>C maps to NM_020318.2 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:226125176 C>T maps to NM_003240.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:226125176 C>T maps to NM_003240.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:248813408 G>A maps to NM_001001824.1 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr1:248813408 G>A maps to NM_001001824.1 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr11:59245249 G>A maps to NM_001004705.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr11:59245249 G>A maps to NM_001004705.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr12:66765506 C>T maps to ENST00000359742 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr12:66765506 C>T maps to ENST00000359742 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr14:20873723 C>G maps to NM_007110.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr14:20873723 C>G maps to NM_007110.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr14:26941561 A>C maps to ENST00000449198 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr14:26941561 A>C maps to ENST00000449198 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr14:64430684 T>C maps to NM_182914.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr14:64430684 T>C maps to NM_182914.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr15:56132879 G>A maps to ENST00000508342 N1047N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr15:56132879 G>A maps to ENST00000508342 N1047N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:35633949 A>G maps to NM_198834.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:35633949 A>G maps to NM_198834.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:48263378 G>A maps to NM_000088.3 F1336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:48263378 G>A maps to NM_000088.3 F1336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:48757177 G>A maps to NM_003786.3 W1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:48757177 G>A maps to NM_003786.3 W1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:70120350 C>T maps to NM_000346.3 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:70120350 C>T maps to NM_000346.3 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:78083808 G>A maps to NM_001079804.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr17:78083808 G>A maps to NM_001079804.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr18:12274237 C>T maps to ENST00000342845 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr18:12274237 C>T maps to ENST00000342845 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr19:4817810 G>A maps to NM_182919.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr19:4817810 G>A maps to NM_182919.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr19:9084686 G>A maps to NM_024690.2 T2376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr19:9084686 G>A maps to NM_024690.2 T2376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr2:74598789 C>T maps to NM_004082.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr2:74598789 C>T maps to NM_004082.4 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr2:179446666 G>A maps to NM_133378.4 D19575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr2:179446666 G>A maps to NM_133378.4 D19575D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr22:50717404 G>A maps to NM_012401.2 D1475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr22:50717404 G>A maps to NM_012401.2 D1475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:36779979 G>A maps to NM_033403.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:36779979 G>A maps to NM_033403.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:37360646 C>T maps to NM_001172713.1 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:37360646 C>T maps to NM_001172713.1 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:42567436 G>A maps to NM_004624.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:42567436 G>A maps to NM_004624.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:51746532 C>T maps to NM_000839.3 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:51746532 C>T maps to NM_000839.3 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:137890531 G>A maps to NM_016216.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr3:137890531 G>A maps to NM_016216.3 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr4:49040169 A>C maps to NM_025087.2 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr4:49040169 A>C maps to NM_025087.2 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr5:67591245 A>G did not map to a codon.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr5:101709073 T>C maps to NM_173488.3 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr5:101709073 T>C maps to NM_173488.3 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr6:38256067 C>T maps to NM_052893.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr6:38256067 C>T maps to NM_052893.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr6:83847934 T>C maps to NM_015018.2 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr6:83847934 T>C maps to NM_015018.2 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr7:50468240 C>A maps to NM_006060.3 C492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr7:50468240 C>A maps to NM_006060.3 C492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr7:97944873 T>C maps to NM_018842.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr7:97944873 T>C maps to NM_018842.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:25718726 G>A maps to NM_022659.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:25718726 G>A maps to NM_022659.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:56866430 T>C maps to NM_002350.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:56866430 T>C maps to NM_002350.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:70980584 T>C maps to NM_024504.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:70980584 T>C maps to NM_024504.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:101730506 C>T maps to NM_002568.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:101730506 C>T maps to NM_002568.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:104778687 T>C maps to NM_001100117.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr8:104778687 T>C maps to NM_001100117.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr9:14775891 C>T maps to ENST00000380880 G1587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr9:14775891 C>T maps to ENST00000380880 G1587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr9:95738834 C>T maps to NM_033086.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr9:95738834 C>T maps to NM_033086.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr9:137777088 G>A maps to NM_004108.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chr9:137777088 G>A maps to NM_004108.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chrX:123220475 C>T maps to NM_001042750.1 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chrX:123220475 C>T maps to NM_001042750.1 R1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chrX:153129350 G>A maps to NM_000425.3 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5955-01A-11D-1696-08 chrX:153129350 G>A maps to NM_000425.3 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr1:40960710 G>A maps to NM_198494.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr1:40960710 G>A maps to NM_198494.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr11:209870 G>A maps to NM_021932.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr11:209870 G>A maps to NM_021932.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr11:5142007 C>T maps to NM_001005222.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr11:5142007 C>T maps to NM_001005222.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr12:130833882 T>A maps to NM_004764.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr12:130833882 T>A maps to NM_004764.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr13:110436117 C>T maps to NM_003749.2 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr13:110436117 C>T maps to NM_003749.2 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr14:57949811 G>A maps to NM_018168.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr14:57949811 G>A maps to NM_018168.2 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr15:25924505 A>T maps to NM_024490.3 S1494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr15:25924505 A>T maps to NM_024490.3 S1494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr16:4731588 G>A maps to NM_015246.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr16:4731588 G>A maps to NM_015246.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr17:27182171 A>G maps to NM_005702.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr17:27182171 A>G maps to NM_005702.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr19:10398452 G>A maps to NM_001544.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr19:10398452 G>A maps to NM_001544.3 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr19:43766195 G>A maps to NM_002784.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr19:43766195 G>A maps to NM_002784.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr2:44152272 C>A maps to NM_133259.3 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr2:44152272 C>A maps to NM_133259.3 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr4:78650008 T>C maps to ENST00000512485 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr4:78650008 T>C maps to ENST00000512485 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr5:149924999 C>T maps to NM_001543.4 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr5:149924999 C>T maps to NM_001543.4 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr5:150512088 G>A maps to NM_001155.4 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr5:150512088 G>A maps to NM_001155.4 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr8:119593040 A>T maps to NM_207506.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5958-01A-11D-1696-08 chr8:119593040 A>T maps to NM_207506.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:2234791 G>A maps to NM_003036.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:2234791 G>A maps to NM_003036.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:42048029 C>T maps to NM_024503.3 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:42048029 C>T maps to NM_024503.3 E813E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:55527066 G>A maps to NM_174936.3 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:55527066 G>A maps to NM_174936.3 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:59041859 C>T maps to NM_002353.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:59041859 C>T maps to NM_002353.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:197889247 C>T maps to NM_020204.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:197889247 C>T maps to NM_020204.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:228509733 G>A maps to NM_001098623.1 A5064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr1:228509733 G>A maps to NM_001098623.1 A5064A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr10:70644149 C>T maps to NM_001130161.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr10:70644149 C>T maps to NM_001130161.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr11:61249364 C>T maps to NM_145017.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr11:61249364 C>T maps to NM_145017.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr11:74979942 C>T maps to NM_004041.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr11:74979942 C>T maps to NM_004041.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr12:13716217 G>C maps to NM_000834.3 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr12:13716217 G>C maps to NM_000834.3 A1318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr14:20443958 C>T maps to NM_001005486.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr14:20443958 C>T maps to NM_001005486.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr14:21871174 C>T did not map to a codon.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr14:21871174 C>T did not map to a codon.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:68643616 G>A maps to ENST00000423218 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:68643616 G>A maps to ENST00000423218 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:75980090 C>T maps to NM_001897.4 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:75980090 C>T maps to NM_001897.4 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:76430101 C>T maps to NM_152335.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:76430101 C>T maps to NM_152335.2 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:81429011 C>T maps to ENST00000458088 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr15:81429011 C>T maps to ENST00000458088 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr16:10788508 C>T maps to NM_144674.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr16:10788508 C>T maps to NM_144674.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr19:6534935 C>T maps to NM_003811.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr19:6534935 C>T maps to NM_003811.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr19:11361719 G>A maps to ENST00000319867 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr19:11361719 G>A maps to ENST00000319867 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr20:32000202 C>T maps to NM_003098.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr20:32000202 C>T maps to NM_003098.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr20:62178624 C>T maps to NM_080823.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr20:62178624 C>T maps to NM_080823.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr3:46542292 C>T maps to NM_031440.1 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr3:46542292 C>T maps to NM_031440.1 Y201Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr3:52563291 G>A maps to NM_001134231.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr3:52563291 G>A maps to NM_001134231.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr3:146177633 C>T did not map to a codon.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr3:146177633 C>T did not map to a codon.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr4:47864931 T>C maps to NM_152995.4 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr4:47864931 T>C maps to NM_152995.4 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr4:48069655 A>T maps to NM_003328.2 *528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr4:48069655 A>T maps to NM_003328.2 *528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr5:19503218 C>G did not map to a codon.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr5:19503218 C>G did not map to a codon.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr5:26881625 G>A maps to NM_016279.3 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr5:26881625 G>A maps to NM_016279.3 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr5:174869391 G>A maps to NM_000794.3 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr5:174869391 G>A maps to NM_000794.3 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr7:103338350 G>A maps to ENST00000428762 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr7:103338350 G>A maps to ENST00000428762 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr7:150069841 G>A maps to NM_001099695.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr7:150069841 G>A maps to NM_001099695.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr8:30701171 G>A maps to NM_031271.3 R1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr8:30701171 G>A maps to NM_031271.3 R1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr8:95792642 G>A maps to NM_181787.2 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr8:95792642 G>A maps to NM_181787.2 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr8:122641442 A>G maps to NM_005328.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr8:122641442 A>G maps to NM_005328.2 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr9:99799548 C>T maps to NM_001333.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chr9:99799548 C>T maps to NM_001333.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chrX:31089935 G>A maps to NM_031894.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chrX:31089935 G>A maps to NM_031894.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chrX:135431774 C>T maps to NM_153834.3 D1970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5959-01A-11D-1696-08 chrX:135431774 C>T maps to NM_153834.3 D1970D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr1:91840985 C>T maps to NM_001017975.3 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr1:91840985 C>T maps to NM_001017975.3 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr11:118133276 G>A maps to NM_144765.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr11:118133276 G>A maps to NM_144765.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr13:88329406 C>T maps to NM_015567.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr13:88329406 C>T maps to NM_015567.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr22:20131183 C>T maps to NM_013373.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr22:20131183 C>T maps to NM_013373.3 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr3:42242441 C>T maps to NM_001042646.1 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr3:42242441 C>T maps to NM_001042646.1 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr3:189587159 C>T maps to NM_003722.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr3:189587159 C>T maps to NM_003722.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr5:176519768 G>A maps to NM_213647.1 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr5:176519768 G>A maps to NM_213647.1 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr6:170880496 G>A did not map to a codon.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr6:170880496 G>A did not map to a codon.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr8:80954869 C>T maps to NM_001025252.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr8:80954869 C>T maps to NM_001025252.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr9:97401547 G>C maps to NM_001127628.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr9:97401547 G>C maps to NM_001127628.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr9:139818448 G>A maps to ENST00000359662 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-19-5960-01A-11D-1696-08 chr9:139818448 G>A maps to ENST00000359662 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr1:161253487 C>T maps to NM_001102566.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr1:161253487 C>T maps to NM_001102566.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr1:183261947 G>A maps to NM_015039.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr1:183261947 G>A maps to NM_015039.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr10:103825335 T>C maps to NM_024747.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr10:103825335 T>C maps to NM_024747.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr11:67225126 C>T maps to NM_145200.3 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr11:67225126 C>T maps to NM_145200.3 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr13:114294536 C>T maps to NM_007111.4 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr13:114294536 C>T maps to NM_007111.4 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr15:52902144 A>G maps to NM_019600.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr15:52902144 A>G maps to NM_019600.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr16:56865909 G>A maps to NM_014669.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr16:56865909 G>A maps to NM_014669.3 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:5418261 G>A maps to NM_033004.3 Q1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:5418261 G>A maps to NM_033004.3 Q1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:7708676 C>T maps to NM_020877.2 N3136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:7708676 C>T maps to NM_020877.2 N3136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:18833932 C>T maps to NM_002767.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:18833932 C>T maps to NM_002767.2 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:28537541 G>A maps to ENST00000394821 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr17:28537541 G>A maps to ENST00000394821 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr19:17017834 G>A maps to ENST00000443236 Y1375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr19:17017834 G>A maps to ENST00000443236 Y1375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr19:43373122 A>C maps to NM_006905.2 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr19:43373122 A>C maps to NM_006905.2 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr2:71160171 G>A maps to NM_012476.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr2:71160171 G>A maps to NM_012476.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr22:17600850 C>T maps to NM_031890.3 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr22:17600850 C>T maps to NM_031890.3 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr4:155242235 A>G maps to NM_017639.3 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr4:155242235 A>G maps to NM_017639.3 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr5:135692415 G>A maps to NM_020389.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr5:135692415 G>A maps to NM_020389.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr6:45390684 G>A maps to ENST00000359524 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr6:45390684 G>A maps to ENST00000359524 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr7:44100418 G>T maps to NM_001122956.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr7:44100418 G>T maps to NM_001122956.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr7:53103949 T>C maps to NM_182595.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr7:53103949 T>C maps to NM_182595.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr7:100404059 C>T maps to NM_004444.4 W822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr7:100404059 C>T maps to NM_004444.4 W822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr8:144993830 C>T maps to NM_201380.2 A3523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1439-01A-01D-1353-08 chr8:144993830 C>T maps to NM_201380.2 A3523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr1:43778132 C>T maps to NM_005424.2 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr1:43778132 C>T maps to NM_005424.2 N596N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr1:182920518 A>T maps to ENST00000287709 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr1:182920518 A>T maps to ENST00000287709 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr11:5602309 C>A maps to NM_001005162.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr11:5602309 C>A maps to NM_001005162.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr12:48529141 G>A maps to NM_001166686.1 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr12:48529141 G>A maps to NM_001166686.1 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr12:56087908 T>C did not map to a codon.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr12:56087908 T>C did not map to a codon.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr12:124116940 T>C maps to NM_001414.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr12:124116940 T>C maps to NM_001414.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr14:64540770 T>C maps to NM_182914.2 L3595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr14:64540770 T>C maps to NM_182914.2 L3595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr17:11696845 T>C maps to NM_001372.3 C2696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr17:11696845 T>C maps to NM_001372.3 C2696C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr17:65862639 A>G maps to ENST00000321892 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr17:65862639 A>G maps to ENST00000321892 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr19:57328399 G>A maps to NM_006210.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr19:57328399 G>A maps to NM_006210.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr2:198318367 G>A maps to NM_025147.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr2:198318367 G>A maps to NM_025147.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr3:47755964 G>A maps to NM_003074.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr3:47755964 G>A maps to NM_003074.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr3:137799415 T>C maps to NM_173543.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr3:137799415 T>C maps to NM_173543.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr4:189068015 C>T maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr4:189068015 C>T maps to NM_178556.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr7:44747272 A>G maps to ENST00000444676 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr7:44747272 A>G maps to ENST00000444676 Q978Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr8:37611536 T>C maps to NM_007175.6 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr8:37611536 T>C maps to NM_007175.6 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr8:98863638 G>A maps to ENST00000378722 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-1442-01A-01D-1696-08 chr8:98863638 G>A maps to ENST00000378722 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr1:39907986 C>T maps to ENST00000361689 R4256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr1:39907986 C>T maps to ENST00000361689 R4256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr1:147230551 G>A maps to NM_005266.5 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr1:147230551 G>A maps to NM_005266.5 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr1:150318610 G>A maps to NM_004698.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr1:150318610 G>A maps to NM_004698.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr10:89720649 G>A did not map to a codon.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr10:89720649 G>A did not map to a codon.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr11:21596531 T>C maps to NM_006157.3 C799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr11:21596531 T>C maps to NM_006157.3 C799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr12:43771194 G>C maps to ENST00000389420 A1656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr12:43771194 G>C maps to ENST00000389420 A1656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr17:27287690 T>A did not map to a codon.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr17:27287690 T>A did not map to a codon.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr17:39724627 G>A maps to NM_000226.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr17:39724627 G>A maps to NM_000226.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr19:42352996 C>T maps to ENST00000427618 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr19:42352996 C>T maps to ENST00000427618 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr20:23065458 G>A maps to NM_012072.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr20:23065458 G>A maps to NM_012072.3 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr5:33576572 G>A maps to NM_030955.2 D1186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr5:33576572 G>A maps to NM_030955.2 D1186D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr6:26247187 C>T maps to NM_003547.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr6:26247187 C>T maps to NM_003547.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr6:43470019 G>T did not map to a codon.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr6:43470019 G>T did not map to a codon.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr7:149431066 A>T maps to NM_032534.2 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr7:149431066 A>T maps to NM_032534.2 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr9:95841845 C>T maps to NM_145006.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chr9:95841845 C>T maps to NM_145006.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chrX:70341429 C>T maps to ENST00000333646 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5132-01A-01D-1486-08 chrX:70341429 C>T maps to ENST00000333646 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr1:150771720 G>A maps to NM_000396.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr1:150771720 G>A maps to NM_000396.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr1:201021761 G>A maps to NM_000069.2 I1292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr1:201021761 G>A maps to NM_000069.2 I1292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr10:55591166 T>C maps to NM_001142763.1 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr10:55591166 T>C maps to NM_001142763.1 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr12:45823036 G>A maps to NM_001025356.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr12:45823036 G>A maps to NM_001025356.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr16:727862 G>A maps to NM_003961.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr16:727862 G>A maps to NM_003961.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr16:15690711 C>T maps to NM_014647.3 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr16:15690711 C>T maps to NM_014647.3 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr17:39551110 G>A maps to ENST00000393998 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr17:39551110 G>A maps to ENST00000393998 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr19:10288041 A>G maps to NM_001130823.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr19:10288041 A>G maps to NM_001130823.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr19:39915858 T>G maps to NM_022835.2 A1362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr19:39915858 T>G maps to NM_022835.2 A1362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr19:56423466 G>A maps to NM_176810.2 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr19:56423466 G>A maps to NM_176810.2 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr2:669580 C>T maps to NM_152834.2 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr2:669580 C>T maps to NM_152834.2 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr2:11750921 G>A maps to NM_014668.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr2:11750921 G>A maps to NM_014668.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr2:21225762 T>C maps to NM_000384.2 R4177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr2:21225762 T>C maps to NM_000384.2 R4177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr21:46875767 C>T maps to ENST00000359759 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr21:46875767 C>T maps to ENST00000359759 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr3:63898471 C>T maps to NM_001177387.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr3:63898471 C>T maps to NM_001177387.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr4:6865691 C>T maps to NM_014743.2 Q1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr4:6865691 C>T maps to NM_014743.2 Q1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr4:152592378 G>A maps to NM_004564.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr4:152592378 G>A maps to NM_004564.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr4:159603467 T>C maps to NM_004453.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr4:159603467 T>C maps to NM_004453.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr6:34004116 C>T maps to NM_000841.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr6:34004116 C>T maps to NM_000841.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr7:99711353 G>A maps to ENST00000472509 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chr7:99711353 G>A maps to ENST00000472509 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chrX:1719769 C>T maps to NM_005088.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chrX:1719769 C>T maps to NM_005088.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chrX:71522707 C>T maps to NM_001144885.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5133-01A-01D-1486-08 chrX:71522707 C>T maps to NM_001144885.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr1:40431622 T>C maps to NM_001136493.1 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr1:40431622 T>C maps to NM_001136493.1 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr11:56085868 A>G maps to NM_001005202.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr11:56085868 A>G maps to NM_001005202.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr11:124618350 G>A maps to NM_014312.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr11:124618350 G>A maps to NM_014312.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr14:71540386 C>T maps to NM_014982.2 R1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr14:71540386 C>T maps to NM_014982.2 R1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr14:89168804 G>A maps to ENST00000380664 Y741Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr14:89168804 G>A maps to ENST00000380664 Y741Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr15:35168174 C>T maps to NM_014691.2 Q1066Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr15:35168174 C>T maps to NM_014691.2 Q1066Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr15:69324093 G>T maps to NM_024505.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr15:69324093 G>T maps to NM_024505.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr17:1419766 C>G maps to NM_016532.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr17:1419766 C>G maps to NM_016532.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr19:3179827 C>T maps to NM_003775.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr19:3179827 C>T maps to NM_003775.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr19:38103689 C>T maps to NM_152606.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr19:38103689 C>T maps to NM_152606.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr2:37376026 C>T did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr2:37376026 C>T did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr2:175432646 A>C maps to NM_003387.4 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr2:175432646 A>C maps to NM_003387.4 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr20:13260545 G>T did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr20:13260545 G>T did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr3:47147484 A>G did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr3:47147484 A>G did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr5:140215866 G>A maps to NM_018910.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr5:140215866 G>A maps to NM_018910.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr6:30131440 C>T did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr6:30131440 C>T did not map to a codon.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr6:151281412 G>A maps to NM_015440.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr6:151281412 G>A maps to NM_015440.3 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr7:93519536 G>A maps to NM_006528.2 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr7:93519536 G>A maps to NM_006528.2 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr7:100841599 C>T maps to NM_178176.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr7:100841599 C>T maps to NM_178176.2 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr9:102590644 T>C maps to NM_173200.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5134-01A-01D-1486-08 chr9:102590644 T>C maps to NM_173200.1 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr1:32084852 G>A maps to NM_001525.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr1:32084852 G>A maps to NM_001525.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr1:153927549 G>A maps to NM_181715.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr1:153927549 G>A maps to NM_181715.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr1:167096395 G>A maps to NM_001080426.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr1:167096395 G>A maps to NM_001080426.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr10:29751330 C>T did not map to a codon.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr10:29751330 C>T did not map to a codon.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr11:1250505 C>T maps to ENST00000447027 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr11:1250505 C>T maps to ENST00000447027 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr12:14650694 G>A maps to NM_018179.3 K1167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr12:14650694 G>A maps to NM_018179.3 K1167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr12:53512676 G>A maps to NM_003578.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr12:53512676 G>A maps to NM_003578.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr13:107187288 C>A maps to NM_004093.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr13:107187288 C>A maps to NM_004093.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr15:40758214 C>T maps to NM_014952.3 D743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr15:40758214 C>T maps to NM_014952.3 D743D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr16:3119232 C>T maps to ENST00000416912 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr16:3119232 C>T maps to ENST00000416912 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr16:75564024 G>A maps to NM_024533.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr16:75564024 G>A maps to NM_024533.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr17:27010833 G>A maps to NM_003170.3 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr17:27010833 G>A maps to NM_003170.3 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr19:9062080 G>C maps to NM_024690.2 S8455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr19:9062080 G>C maps to NM_024690.2 S8455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr19:17945946 C>T maps to NM_000215.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr19:17945946 C>T maps to NM_000215.3 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr19:38572328 C>T maps to NM_015073.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr19:38572328 C>T maps to NM_015073.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr20:43922451 C>T maps to ENST00000372754 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr20:43922451 C>T maps to ENST00000372754 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr3:184021748 T>C maps to NM_002808.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr3:184021748 T>C maps to NM_002808.3 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr5:1216783 C>T maps to NM_001003841.2 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr5:1216783 C>T maps to NM_001003841.2 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr5:45262135 G>A maps to NM_021072.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr5:45262135 G>A maps to NM_021072.2 R854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr5:71634537 C>T maps to NM_024754.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr5:71634537 C>T maps to NM_024754.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr6:29797339 G>C maps to ENST00000376828 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr6:29797339 G>C maps to ENST00000376828 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr6:36564706 C>T maps to NM_003017.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr6:36564706 C>T maps to NM_003017.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr7:15425166 G>A maps to NM_001004320.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr7:15425166 G>A maps to NM_001004320.1 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr7:106508578 C>T maps to NM_002649.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr7:106508578 C>T maps to NM_002649.2 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr7:127222595 G>A maps to NM_024523.5 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr7:127222595 G>A maps to NM_024523.5 D600D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr8:24324410 G>A maps to ENST00000380789 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr8:24324410 G>A maps to ENST00000380789 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr8:125568544 G>A maps to NM_014751.4 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr8:125568544 G>A maps to NM_014751.4 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr9:135946655 G>C maps to NM_001807.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr9:135946655 G>C maps to NM_001807.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr9:136217155 C>T maps to NM_000972.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5135-01A-01D-1486-08 chr9:136217155 C>T maps to NM_000972.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:9780230 C>T maps to ENST00000361110 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:9780230 C>T maps to ENST00000361110 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:143767629 G>A maps to NM_001123068.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:143767629 G>A maps to NM_001123068.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:156879621 C>T maps to NM_001080471.1 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:156879621 C>T maps to NM_001080471.1 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:232561419 G>A maps to NM_020808.3 N1515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:232561419 G>A maps to NM_020808.3 N1515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:232626678 G>A maps to NM_020808.3 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr1:232626678 G>A maps to NM_020808.3 R583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr11:101762249 C>T maps to NM_178127.4 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr11:101762249 C>T maps to NM_178127.4 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr12:3389624 C>T maps to ENST00000407263 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr12:3389624 C>T maps to ENST00000407263 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr13:96530053 T>C maps to NM_020121.3 Q1095Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr13:96530053 T>C maps to NM_020121.3 Q1095Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr15:90226619 C>T maps to NM_003847.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr15:90226619 C>T maps to NM_003847.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr18:5415837 C>T maps to NM_012307.2 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr18:5415837 C>T maps to NM_012307.2 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr2:238270474 C>G did not map to a codon.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr2:238270474 C>G did not map to a codon.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr4:69696491 G>T maps to NM_001075.4 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr4:69696491 G>T maps to NM_001075.4 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr4:89941641 C>T maps to NM_014883.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr4:89941641 C>T maps to NM_014883.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr6:44217320 G>T did not map to a codon.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr6:44217320 G>T did not map to a codon.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr7:66262469 T>C maps to ENST00000451741 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr7:66262469 T>C maps to ENST00000451741 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr7:103389895 T>C maps to ENST00000428762 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chr7:103389895 T>C maps to ENST00000428762 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:11790273 G>A did not map to a codon.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:11790273 G>A did not map to a codon.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:47069359 G>C maps to NM_153280.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:47069359 G>C maps to NM_153280.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:48814295 G>A maps to NM_017602.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:48814295 G>A maps to NM_017602.3 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:69871357 G>A maps to NM_001003811.1 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:69871357 G>A maps to NM_001003811.1 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:109247263 G>T maps to NM_032227.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5136-01B-01D-1486-08 chrX:109247263 G>T maps to NM_032227.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr1:151149179 A>T maps to ENST00000354473 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr1:151149179 A>T maps to ENST00000354473 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr1:157804443 G>A maps to NM_005894.2 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr1:157804443 G>A maps to NM_005894.2 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:7061223 G>A maps to ENST00000416215 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:7061223 G>A maps to ENST00000416215 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:43823482 G>A maps to ENST00000389420 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:43823482 G>A maps to ENST00000389420 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:89917756 G>T maps to NM_003774.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:89917756 G>T maps to NM_003774.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:109495848 C>A maps to NM_032663.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr12:109495848 C>A maps to NM_032663.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr15:41501707 G>A maps to NM_152596.2 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr15:41501707 G>A maps to NM_152596.2 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr18:28989413 G>A did not map to a codon.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr18:28989413 G>A did not map to a codon.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr18:30950073 G>C maps to NM_001105528.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr18:30950073 G>C maps to NM_001105528.1 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr18:61262396 C>T maps to NM_012397.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr18:61262396 C>T maps to NM_012397.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr19:40395989 G>A maps to NM_003890.2 F2469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr19:40395989 G>A maps to NM_003890.2 F2469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr2:1926964 G>A maps to ENST00000399161 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr2:1926964 G>A maps to ENST00000399161 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr3:50385754 G>A maps to NM_006545.4 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr3:50385754 G>A maps to NM_006545.4 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr4:956665 C>A maps to NM_001347.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr4:956665 C>A maps to NM_001347.2 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr4:155241879 C>T maps to NM_017639.3 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr4:155241879 C>T maps to NM_017639.3 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr5:137275997 C>T maps to NM_016603.2 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr5:137275997 C>T maps to NM_016603.2 E888E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr7:5340250 C>T maps to NM_153247.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr7:5340250 C>T maps to NM_153247.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr7:75068438 G>T maps to ENST00000257665 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr7:75068438 G>T maps to ENST00000257665 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr8:42587373 C>A maps to NM_000749.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr8:42587373 C>A maps to NM_000749.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr8:110984559 G>A maps to NM_014379.2 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chr8:110984559 G>A maps to NM_014379.2 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chrX:54319680 T>C maps to NM_020922.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chrX:54319680 T>C maps to NM_020922.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chrX:100611219 G>A maps to NM_000061.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-5139-01A-01D-1486-08 chrX:100611219 G>A maps to NM_000061.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr1:152777633 G>A maps to NM_178351.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr1:152777633 G>A maps to NM_178351.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr11:46783672 T>C maps to ENST00000415402 K1366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr11:46783672 T>C maps to ENST00000415402 K1366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr11:59828704 G>A maps to NM_006138.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr11:59828704 G>A maps to NM_006138.4 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr12:12483053 G>A maps to NM_018050.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr12:12483053 G>A maps to NM_018050.2 L401L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-26-6173-01A-11D-1845-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-26-6173-01A-11D-1845-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr17:10304644 T>A maps to NM_002472.2 K1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr17:10304644 T>A maps to NM_002472.2 K1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr19:54609316 A>C maps to NM_004542.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr19:54609316 A>C maps to NM_004542.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr2:144381720 C>T maps to NM_018460.3 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr2:144381720 C>T maps to NM_018460.3 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr2:207174441 G>A maps to NM_020923.1 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr2:207174441 G>A maps to NM_020923.1 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr3:47040320 C>T maps to NM_015175.1 V1112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr3:47040320 C>T maps to NM_015175.1 V1112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr3:173525620 C>T maps to NM_014932.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr3:173525620 C>T maps to NM_014932.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr4:10522451 A>G maps to NM_052964.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr4:10522451 A>G maps to NM_052964.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr4:42080308 A>G maps to NM_006345.3 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr4:42080308 A>G maps to NM_006345.3 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr4:71255516 C>T maps to NM_006685.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr4:71255516 C>T maps to NM_006685.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr5:161128646 C>A maps to NM_000811.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr5:161128646 C>A maps to NM_000811.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr6:117638304 C>T did not map to a codon.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr6:117638304 C>T did not map to a codon.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr8:143960554 G>A maps to ENST00000377675 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr8:143960554 G>A maps to ENST00000377675 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr9:140809199 C>T maps to ENST00000277549 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6173-01A-11D-1845-08 chr9:140809199 C>T maps to ENST00000277549 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr1:29606626 G>A maps to NM_005704.4 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr1:29606626 G>A maps to NM_005704.4 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr1:93298989 C>A maps to NM_000969.3 Y16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr1:93298989 C>A maps to NM_000969.3 Y16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr1:115401211 G>A maps to NM_003176.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr1:115401211 G>A maps to NM_003176.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr12:70974842 G>A maps to NM_001109754.1 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr12:70974842 G>A maps to NM_001109754.1 R851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr13:43175076 T>A maps to NM_003701.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr13:43175076 T>A maps to NM_003701.3 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr16:24202547 A>G maps to NM_002738.6 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr16:24202547 A>G maps to NM_002738.6 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr16:81095125 G>A maps to NM_152337.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr16:81095125 G>A maps to NM_152337.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr16:85120719 G>A maps to NM_014732.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr16:85120719 G>A maps to NM_014732.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr19:7676674 G>A maps to NM_001080429.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr19:7676674 G>A maps to NM_001080429.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr20:30065685 C>T maps to NM_014012.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr20:30065685 C>T maps to NM_014012.4 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr3:89259059 C>G maps to NM_005233.5 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr3:89259059 C>G maps to NM_005233.5 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr3:97852368 A>G maps to NM_001005338.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr3:97852368 A>G maps to NM_001005338.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:50091079 A>G maps to ENST00000505697 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:50091079 A>G maps to ENST00000505697 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:55083702 T>C maps to NM_024415.2 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:55083702 T>C maps to NM_024415.2 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:140263907 C>T maps to NM_018904.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:140263907 C>T maps to NM_018904.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:154393520 C>T maps to NM_001099293.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr5:154393520 C>T maps to NM_001099293.1 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr6:62407127 T>C maps to NM_152688.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr6:62407127 T>C maps to NM_152688.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr7:100451835 C>G maps to NM_020246.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr7:100451835 C>G maps to NM_020246.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr8:141525276 G>A maps to NM_017444.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr8:141525276 G>A maps to NM_017444.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr9:140477433 C>T did not map to a codon.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chr9:140477433 C>T did not map to a codon.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chrX:115592952 A>C maps to NM_001017978.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chrX:115592952 A>C maps to NM_001017978.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chrX:138668561 C>T maps to ENST00000370578 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chrX:138668561 C>T maps to ENST00000370578 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chrX:148564456 G>T maps to NM_000202.5 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-26-6174-01A-21D-1845-08 chrX:148564456 G>T maps to NM_000202.5 S491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr1:32163659 C>T maps to NM_001856.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr1:32163659 C>T maps to NM_001856.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr1:59805656 C>T maps to NM_001113411.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr1:59805656 C>T maps to NM_001113411.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr10:61836045 C>T maps to NM_020987.2 T1531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr10:61836045 C>T maps to NM_020987.2 T1531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr11:36596876 C>T maps to NM_000448.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr11:36596876 C>T maps to NM_000448.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr11:49186292 C>T maps to NM_004476.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr11:49186292 C>T maps to NM_004476.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:6127887 G>A maps to NM_000552.3 R1566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:6127887 G>A maps to NM_000552.3 R1566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:7528294 C>T did not map to a codon.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:7528294 C>T did not map to a codon.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:53294404 G>A maps to NM_002273.3 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:53294404 G>A maps to NM_002273.3 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:66597511 G>A maps to NM_007199.2 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:66597511 G>A maps to NM_007199.2 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:123794320 C>T maps to NM_001167856.1 A1126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr12:123794320 C>T maps to NM_001167856.1 A1126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr16:1498996 G>A maps to ENST00000382745 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr16:1498996 G>A maps to ENST00000382745 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr16:71509675 G>A maps to NM_006961.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr16:71509675 G>A maps to NM_006961.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr19:18675765 C>T maps to NM_024069.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr19:18675765 C>T maps to NM_024069.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr19:36230668 G>A maps to NM_024660.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr19:36230668 G>A maps to NM_024660.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr2:179410963 G>A maps to NM_133378.4 A29130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr2:179410963 G>A maps to NM_133378.4 A29130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr21:47349907 C>A maps to NM_020528.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr21:47349907 C>A maps to NM_020528.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr3:123457796 G>A maps to NM_053025.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr3:123457796 G>A maps to NM_053025.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr4:119064754 C>T maps to NM_004784.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr4:119064754 C>T maps to NM_004784.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr5:70945047 C>T maps to NM_022132.4 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr5:70945047 C>T maps to NM_022132.4 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr5:131729365 A>G did not map to a codon.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr5:131729365 A>G did not map to a codon.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr5:162945326 T>G maps to NM_013283.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr5:162945326 T>G maps to NM_013283.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr6:82924065 A>C maps to NM_015525.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr6:82924065 A>C maps to NM_015525.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr7:88966246 A>G maps to NM_181646.2 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr7:88966246 A>G maps to NM_181646.2 V1317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr7:150171328 G>A maps to NM_175571.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1830-01A-01W-0643-08 chr7:150171328 G>A maps to NM_175571.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr1:15904245 G>A maps to NM_024758.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr1:15904245 G>A maps to NM_024758.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr1:23520070 G>A maps to NM_000864.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr1:23520070 G>A maps to NM_000864.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr1:237863750 C>T maps to NM_001035.2 F3117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr1:237863750 C>T maps to NM_001035.2 F3117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr11:64521010 G>A maps to NM_005609.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr11:64521010 G>A maps to NM_005609.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr12:13716352 C>T maps to NM_000834.3 T1273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr12:13716352 C>T maps to NM_000834.3 T1273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr12:91363837 G>A maps to NM_004950.4 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr12:91363837 G>A maps to NM_004950.4 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr15:74238820 C>T maps to NM_005576.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr15:74238820 C>T maps to NM_005576.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr17:5050404 C>T maps to NM_004505.2 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr17:5050404 C>T maps to NM_004505.2 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr2:157407114 G>A maps to NM_000408.4 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr2:157407114 G>A maps to NM_000408.4 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr2:226447518 G>A maps to NM_020864.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr2:226447518 G>A maps to NM_020864.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr2:238275629 C>A maps to NM_004369.3 E1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr2:238275629 C>A maps to NM_004369.3 E1734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr4:38830722 C>T maps to NM_006068.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr4:38830722 C>T maps to NM_006068.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr4:147824705 G>A maps to ENST00000513335 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr4:147824705 G>A maps to ENST00000513335 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr7:99669055 G>A maps to NM_032924.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr7:99669055 G>A maps to NM_032924.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr7:128355632 G>A maps to NM_032599.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr7:128355632 G>A maps to NM_032599.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr8:103289357 C>T maps to NM_015902.4 R2117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1831-01A-01D-1494-08 chr8:103289357 C>T maps to NM_015902.4 R2117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr11:59947357 G>A maps to NM_152852.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr11:59947357 G>A maps to NM_152852.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr12:125599072 C>A maps to NM_023928.3 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr12:125599072 C>A maps to NM_023928.3 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr13:113793674 C>T maps to NM_000504.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr13:113793674 C>T maps to NM_000504.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr16:1306640 C>T maps to NM_012217.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr16:1306640 C>T maps to NM_012217.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr16:20975341 G>A maps to NM_017539.1 D3288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr16:20975341 G>A maps to NM_017539.1 D3288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr21:45113182 A>C maps to NM_015056.2 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr21:45113182 A>C maps to NM_015056.2 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr22:32546407 C>T maps to NM_001010859.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr22:32546407 C>T maps to NM_001010859.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr3:47307238 G>A maps to NM_182902.3 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr3:47307238 G>A maps to NM_182902.3 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr4:56875925 C>T maps to NM_025009.3 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr4:56875925 C>T maps to NM_025009.3 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr5:74056812 T>C did not map to a codon.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr5:74056812 T>C did not map to a codon.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr5:140167206 G>A maps to NM_018900.2 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr5:140167206 G>A maps to NM_018900.2 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr7:33138994 G>A maps to NM_203288.1 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr7:33138994 G>A maps to NM_203288.1 H79H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr7:76796978 G>A did not map to a codon.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr7:76796978 G>A did not map to a codon.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr7:86998728 G>T maps to NM_001143935.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr7:86998728 G>T maps to NM_001143935.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr9:35045865 G>C maps to NM_203299.2 *1080Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1832-01A-01W-0643-08 chr9:35045865 G>C maps to NM_203299.2 *1080Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr1:74507362 G>A maps to NM_001105659.1 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr1:74507362 G>A maps to NM_001105659.1 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr10:28345468 T>C maps to NM_173496.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr10:28345468 T>C maps to NM_173496.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr10:101147662 C>T maps to NM_020348.2 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr10:101147662 C>T maps to NM_020348.2 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr12:21229465 C>T maps to ENST00000381541 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr12:21229465 C>T maps to ENST00000381541 R584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr12:57642899 G>A maps to NM_145064.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr12:57642899 G>A maps to NM_145064.1 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr16:1255217 C>A maps to NM_021098.2 Y852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr16:1255217 C>A maps to NM_021098.2 Y852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr16:27357788 G>A maps to NM_000418.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr16:27357788 G>A maps to NM_000418.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr17:14140071 G>A maps to NM_001007530.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr17:14140071 G>A maps to NM_001007530.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr17:34416094 G>A maps to NM_002983.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr17:34416094 G>A maps to NM_002983.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr18:5406823 G>A maps to NM_012307.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr18:5406823 G>A maps to NM_012307.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr19:13410022 C>T maps to NM_023035.2 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr19:13410022 C>T maps to NM_023035.2 T812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr19:46094824 A>G maps to NM_005282.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr19:46094824 A>G maps to NM_005282.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr2:232326476 G>T maps to NM_005381.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr2:232326476 G>T maps to NM_005381.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr2:235950762 C>T maps to NM_014521.2 Y450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr2:235950762 C>T maps to NM_014521.2 Y450Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr2:242683166 C>T maps to NM_152783.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr2:242683166 C>T maps to NM_152783.3 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr20:50803593 C>T maps to NM_018197.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr20:50803593 C>T maps to NM_018197.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr20:60921842 G>A maps to NM_005560.3 Y362Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr20:60921842 G>A maps to NM_005560.3 Y362Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr21:19770221 A>G maps to NM_002772.2 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr21:19770221 A>G maps to NM_002772.2 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr22:43089429 G>A maps to NM_017436.4 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr22:43089429 G>A maps to NM_017436.4 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr4:1955108 A>G maps to NM_133335.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr4:1955108 A>G maps to NM_133335.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr6:51523916 C>T maps to NM_138694.3 S3669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr6:51523916 C>T maps to NM_138694.3 S3669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr7:106513285 C>T maps to NM_002649.2 H730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr7:106513285 C>T maps to NM_002649.2 H730H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr7:134260191 C>T maps to ENST00000418096 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr7:134260191 C>T maps to ENST00000418096 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr8:142476585 G>A maps to NM_207414.2 H800H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr8:142476585 G>A maps to NM_207414.2 H800H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr9:140201614 G>A maps to NM_017820.3 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chr9:140201614 G>A maps to NM_017820.3 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chrX:79938108 G>A maps to NM_153252.4 R1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chrX:79938108 G>A maps to NM_153252.4 R1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chrX:102334797 C>T maps to NM_022052.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1833-01A-01W-0643-08 chrX:102334797 C>T maps to NM_022052.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr11:60075608 C>T maps to NM_148975.1 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr11:60075608 C>T maps to NM_148975.1 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr11:66359835 G>A maps to NM_018219.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr11:66359835 G>A maps to NM_018219.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr13:53624554 T>A maps to NM_006418.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr13:53624554 T>A maps to NM_006418.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr14:22102704 C>T maps to NM_001005466.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr14:22102704 C>T maps to NM_001005466.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr14:38060668 G>A maps to NM_004496.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr14:38060668 G>A maps to NM_004496.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr16:24185838 A>T maps to NM_002738.6 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr16:24185838 A>T maps to NM_002738.6 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr17:58678098 C>T maps to NM_003620.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr17:58678098 C>T maps to NM_003620.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr17:70644979 G>A maps to NM_001159770.1 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr17:70644979 G>A maps to NM_001159770.1 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr17:77915924 C>T maps to NM_019020.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr17:77915924 C>T maps to NM_019020.2 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr2:168098386 C>T maps to NM_152381.5 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr2:168098386 C>T maps to NM_152381.5 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr20:54978728 G>A maps to NM_001033522.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr20:54978728 G>A maps to NM_001033522.1 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr3:12881706 G>A maps to ENST00000273223 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr3:12881706 G>A maps to ENST00000273223 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr3:134920350 G>T maps to NM_004441.4 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr3:134920350 G>T maps to NM_004441.4 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr4:79400663 G>A maps to NM_025074.6 G2745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr4:79400663 G>A maps to NM_025074.6 G2745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr5:157078492 G>A maps to NM_178424.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr5:157078492 G>A maps to NM_178424.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:23509594 C>T maps to NM_006547.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:23509594 C>T maps to NM_006547.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:80117946 G>A maps to NM_001102386.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:80117946 G>A maps to NM_001102386.1 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:98554146 C>T maps to ENST00000359863 A2067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:98554146 C>T maps to ENST00000359863 A2067A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:98567835 C>T maps to ENST00000359863 H2531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:98567835 C>T maps to ENST00000359863 H2531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:143043324 G>A maps to NM_000083.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chr7:143043324 G>A maps to NM_000083.2 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chrX:1407664 C>T maps to NM_001161530.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1834-01A-01W-0643-08 chrX:1407664 C>T maps to NM_001161530.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr1:233515029 C>T maps to NM_032435.2 R760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr1:233515029 C>T maps to NM_032435.2 R760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr11:55944235 T>A maps to NM_001005492.1 L48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr11:55944235 T>A maps to NM_001005492.1 L48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr12:8211863 G>A maps to NM_004054.2 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr12:8211863 G>A maps to NM_004054.2 Y306Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr12:112622743 G>A maps to NM_001109662.2 S3170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr12:112622743 G>A maps to NM_001109662.2 S3170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr12:113600991 G>T maps to NM_001111322.1 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr12:113600991 G>T maps to NM_001111322.1 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr14:74991926 C>G maps to NM_000428.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr14:74991926 C>G maps to NM_000428.2 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr17:37265500 C>T maps to NM_020405.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr17:37265500 C>T maps to NM_020405.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr2:108999905 A>T maps to NM_006588.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr2:108999905 A>T maps to NM_006588.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr20:41306568 G>A maps to ENST00000373198 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr20:41306568 G>A maps to ENST00000373198 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr20:43927041 A>T maps to ENST00000372754 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr20:43927041 A>T maps to ENST00000372754 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:1818641 C>T did not map to a codon.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:1818641 C>T did not map to a codon.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:1978377 C>A maps to NM_133335.3 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:1978377 C>A maps to NM_133335.3 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:53468066 C>G maps to NM_022832.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:53468066 C>G maps to NM_022832.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:71024298 G>A maps to NM_214711.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr4:71024298 G>A maps to NM_214711.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr6:111498840 T>C maps to NM_018593.4 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr6:111498840 T>C maps to NM_018593.4 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr6:116938050 G>T maps to NM_001010892.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr6:116938050 G>T maps to NM_001010892.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr6:170599202 G>A maps to NM_005618.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr6:170599202 G>A maps to NM_005618.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr7:37903980 G>C maps to NM_016616.4 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr7:37903980 G>C maps to NM_016616.4 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr7:99693695 C>T maps to NM_005916.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr7:99693695 C>T maps to NM_005916.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr7:100681845 C>T maps to NM_001040105.1 D2383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chr7:100681845 C>T maps to NM_001040105.1 D2383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:20148633 G>A maps to NM_001412.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:20148633 G>A maps to NM_001412.3 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:46359484 G>T maps to NM_001039891.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:46359484 G>T maps to NM_001039891.2 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:107407828 C>A did not map to a codon.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:107407828 C>A did not map to a codon.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:141291590 C>T maps to NM_016249.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1835-01A-01D-1494-08 chrX:141291590 C>T maps to NM_016249.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr1:237777378 C>T maps to NM_001035.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr1:237777378 C>T maps to NM_001035.2 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr11:1094854 C>T maps to ENST00000441003 Y1981Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr11:1094854 C>T maps to ENST00000441003 Y1981Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr11:67223869 C>T maps to NM_145200.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr11:67223869 C>T maps to NM_145200.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr19:3282230 C>T maps to NM_021938.3 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr19:3282230 C>T maps to NM_021938.3 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr2:211070505 A>G maps to NM_001608.3 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr2:211070505 A>G maps to NM_001608.3 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr22:43575871 C>T maps to NM_015140.3 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr22:43575871 C>T maps to NM_015140.3 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr22:46931873 G>A maps to NM_014246.1 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr22:46931873 G>A maps to NM_014246.1 D398D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:42676816 A>G maps to NM_005385.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:42676816 A>G maps to NM_005385.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:67054665 C>T maps to NM_032505.2 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:67054665 C>T maps to NM_032505.2 C425C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:78734959 G>A maps to NM_002941.3 Y426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:78734959 G>A maps to NM_002941.3 Y426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:160395694 G>A maps to NM_025047.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr3:160395694 G>A maps to NM_025047.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr8:9565980 G>A maps to NM_003747.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr8:9565980 G>A maps to NM_003747.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr8:95531631 A>G maps to NM_015496.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr8:95531631 A>G maps to NM_015496.3 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr8:145700406 C>T maps to NM_003923.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1836-01A-01D-1494-08 chr8:145700406 C>T maps to NM_003923.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr12:7302218 C>T maps to NM_014718.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr12:7302218 C>T maps to NM_014718.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr15:67664810 C>T maps to NM_001031715.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr15:67664810 C>T maps to NM_001031715.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr16:25251328 T>C maps to NM_001012981.4 E904E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr16:25251328 T>C maps to NM_001012981.4 E904E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr21:37833393 G>A maps to NM_001146077.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr21:37833393 G>A maps to NM_001146077.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr3:97851849 G>A maps to NM_001005338.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr3:97851849 G>A maps to NM_001005338.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr5:140626804 C>T maps to NM_018935.2 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr5:140626804 C>T maps to NM_018935.2 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr6:134582968 C>T did not map to a codon.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr6:134582968 C>T did not map to a codon.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr7:86415950 G>A maps to NM_000840.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr7:86415950 G>A maps to NM_000840.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr7:103368565 G>A maps to ENST00000428762 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr7:103368565 G>A maps to ENST00000428762 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr8:3216773 C>T maps to NM_033225.5 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chr8:3216773 C>T maps to NM_033225.5 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chrX:57146696 G>A maps to NM_001006683.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1837-01A-01D-1494-08 chrX:57146696 G>A maps to NM_001006683.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr1:94965169 G>A maps to ENST00000454898 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr1:94965169 G>A maps to ENST00000454898 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr1:248129571 G>A maps to NM_001004491.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr1:248129571 G>A maps to NM_001004491.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr10:48429387 C>T maps to NM_004962.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr10:48429387 C>T maps to NM_004962.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr11:55135748 T>C maps to NM_001005275.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr11:55135748 T>C maps to NM_001005275.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr11:61732279 G>C maps to NM_002032.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr11:61732279 G>C maps to NM_002032.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr12:21970189 G>A maps to NM_005691.2 Q1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr12:21970189 G>A maps to NM_005691.2 Q1275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr13:28636173 C>T maps to NM_004119.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr13:28636173 C>T maps to NM_004119.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr14:92343923 G>A maps to ENST00000267620 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr14:92343923 G>A maps to ENST00000267620 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr14:96991693 A>G maps to NM_032632.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr14:96991693 A>G maps to NM_032632.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr17:8644916 G>A maps to NM_144681.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr17:8644916 G>A maps to NM_144681.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr18:64218400 C>T maps to NM_021153.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr18:64218400 C>T maps to NM_021153.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr2:99634811 C>T maps to NM_025244.2 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr2:99634811 C>T maps to NM_025244.2 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr2:168103542 C>T maps to NM_152381.5 R1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr2:168103542 C>T maps to NM_152381.5 R1881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr20:870857 G>A maps to NM_015985.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr20:870857 G>A maps to NM_015985.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr3:32932738 G>A maps to NM_001039111.1 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr3:32932738 G>A maps to NM_001039111.1 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr3:49756784 A>G maps to NM_198722.2 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr3:49756784 A>G maps to NM_198722.2 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr5:140255257 G>A maps to NM_018903.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr5:140255257 G>A maps to NM_018903.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:43413521 G>A maps to NM_033450.2 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:43413521 G>A maps to NM_033450.2 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:52993579 T>C maps to NM_003643.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:52993579 T>C maps to NM_003643.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:63990359 G>A maps to NM_016571.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:63990359 G>A maps to NM_016571.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:64422166 A>G maps to NM_015153.2 R1561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr6:64422166 A>G maps to NM_015153.2 R1561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr7:31009512 C>A maps to NM_000823.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr7:31009512 C>A maps to NM_000823.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr7:82474619 G>A maps to NM_033026.5 P4671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr7:82474619 G>A maps to NM_033026.5 P4671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr8:30040688 A>C maps to NM_006571.2 *191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr8:30040688 A>C maps to NM_006571.2 *191Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr8:38826180 C>T maps to NM_021623.1 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr8:38826180 C>T maps to NM_021623.1 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr8:79645968 C>T maps to NM_000880.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr8:79645968 C>T maps to NM_000880.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr9:95610512 C>A maps to NM_031486.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr9:95610512 C>A maps to NM_031486.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr9:138453718 C>A maps to NM_002571.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chr9:138453718 C>A maps to NM_002571.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:52677323 A>G maps to ENST00000435678 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:52677323 A>G maps to ENST00000435678 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:73963401 C>T maps to NM_001008537.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:73963401 C>T maps to NM_001008537.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:125686303 C>T maps to NM_178470.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:125686303 C>T maps to NM_178470.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:151303933 G>A maps to NM_021048.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-1838-01A-01D-1494-08 chrX:151303933 G>A maps to NM_021048.3 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr1:40150149 G>A maps to NM_016257.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr1:40150149 G>A maps to NM_016257.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr1:205890885 G>A maps to NM_134325.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr1:205890885 G>A maps to NM_134325.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:10327295 C>T maps to NM_001124.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:10327295 C>T maps to NM_001124.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:45671303 C>T maps to NM_003654.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:45671303 C>T maps to NM_003654.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:55541761 G>A maps to NM_001001967.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:55541761 G>A maps to NM_001001967.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:59807921 C>T did not map to a codon.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr11:59807921 C>T did not map to a codon.
Alternatively spliced codon TCGA-27-2518-01A-01D-1494-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-27-2518-01A-01D-1494-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr12:4409082 C>T maps to NM_001759.3 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr12:4409082 C>T maps to NM_001759.3 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr12:65564281 C>A maps to NM_014319.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr12:65564281 C>A maps to NM_014319.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr13:113771869 C>T maps to NM_000131.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr13:113771869 C>T maps to NM_000131.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr14:53217445 C>T maps to NM_145251.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr14:53217445 C>T maps to NM_145251.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr14:94109959 C>T maps to ENST00000393153 A2048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr14:94109959 C>T maps to ENST00000393153 A2048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr14:105418808 G>A maps to NM_138420.2 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr14:105418808 G>A maps to NM_138420.2 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr15:99671204 C>T maps to ENST00000336292 D879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr15:99671204 C>T maps to ENST00000336292 D879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr17:72308275 G>A maps to NM_023036.4 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr17:72308275 G>A maps to NM_023036.4 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:15067439 C>T maps to NM_005071.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:15067439 C>T maps to NM_005071.1 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:43414918 C>T maps to NM_002782.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:43414918 C>T maps to NM_002782.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:52115642 G>A maps to ENST00000222107 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:52115642 G>A maps to ENST00000222107 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:56515207 C>T maps to NM_153447.4 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr19:56515207 C>T maps to NM_153447.4 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr2:95947040 C>T maps to NM_144707.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr2:95947040 C>T maps to NM_144707.2 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr2:228856022 T>A maps to NM_001142644.1 K1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr2:228856022 T>A maps to NM_001142644.1 K1581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr20:62365994 A>C did not map to a codon.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr20:62365994 A>C did not map to a codon.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr22:43600125 G>A maps to NM_173050.2 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr22:43600125 G>A maps to NM_173050.2 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr3:3139659 A>C maps to NM_000564.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr3:3139659 A>C maps to NM_000564.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr3:148868421 G>A maps to NM_032383.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr3:148868421 G>A maps to NM_032383.3 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr5:140589501 C>T maps to NM_018932.3 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr5:140589501 C>T maps to NM_018932.3 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr5:179731783 G>A maps to NM_005110.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr5:179731783 G>A maps to NM_005110.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr5:179731921 G>C maps to NM_005110.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr5:179731921 G>C maps to NM_005110.2 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr8:38148068 G>A maps to NM_023034.1 G1014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr8:38148068 G>A maps to NM_023034.1 G1014G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr8:85774545 C>T maps to NM_001100391.1 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chr8:85774545 C>T maps to NM_001100391.1 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chrX:13727278 C>G maps to NM_004251.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2518-01A-01D-1494-08 chrX:13727278 C>G maps to NM_004251.4 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr12:101480463 C>T maps to ENST00000392977 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr12:101480463 C>T maps to ENST00000392977 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr15:78403608 C>T maps to NM_006383.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr15:78403608 C>T maps to NM_006383.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr18:6859896 G>T did not map to a codon.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr18:6859896 G>T did not map to a codon.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr19:51329906 G>A maps to NM_017509.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr19:51329906 G>A maps to NM_017509.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr2:183066516 C>G did not map to a codon.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr2:183066516 C>G did not map to a codon.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr5:57913621 C>T maps to NM_138453.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr5:57913621 C>T maps to NM_138453.2 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr8:30701171 G>A maps to NM_031271.3 R1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr8:30701171 G>A maps to NM_031271.3 R1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr8:125110085 C>A maps to NM_001039112.2 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr8:125110085 C>A maps to NM_001039112.2 I1615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr9:112153416 C>T did not map to a codon.
Sequencing variant TCGA-27-2519-01A-01D-1494-08 chr9:112153416 C>T did not map to a codon.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:12918956 G>A maps to NM_023014.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:12918956 G>A maps to NM_023014.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:46871971 C>T maps to NM_001441.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:46871971 C>T maps to NM_001441.2 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:170508570 C>T maps to NM_152281.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:170508570 C>T maps to NM_152281.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:198262081 G>A maps to NM_133494.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr1:198262081 G>A maps to NM_133494.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr10:5804608 G>A maps to NM_017782.4 W2430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr10:5804608 G>A maps to NM_017782.4 W2430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr10:28378638 G>A maps to NM_173496.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr10:28378638 G>A maps to NM_173496.3 R362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:45923592 A>T maps to NM_005456.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:45923592 A>T maps to NM_005456.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:111899614 G>A maps to NM_001931.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:111899614 G>A maps to NM_001931.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:113857601 C>A maps to NM_213621.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:113857601 C>A maps to NM_213621.3 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:113857613 G>C maps to NM_213621.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr11:113857613 G>C maps to NM_213621.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr15:49325160 C>G did not map to a codon.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr15:49325160 C>G did not map to a codon.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr18:44554623 C>T maps to NM_145653.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr18:44554623 C>T maps to NM_145653.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr19:2733096 G>A maps to NM_144564.4 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr19:2733096 G>A maps to NM_144564.4 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr2:74328396 C>T maps to ENST00000409262 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr2:74328396 C>T maps to ENST00000409262 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr2:109388155 G>A did not map to a codon.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr2:109388155 G>A did not map to a codon.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr20:13052998 C>G maps to NM_018327.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr20:13052998 C>G maps to NM_018327.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr3:169555373 A>G maps to NM_001080460.1 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr3:169555373 A>G maps to NM_001080460.1 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr5:157065653 G>A maps to NM_178424.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr5:157065653 G>A maps to NM_178424.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:5613544 A>T maps to NM_006567.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:5613544 A>T maps to NM_006567.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:30680500 G>A maps to NM_014641.2 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:30680500 G>A maps to NM_014641.2 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:31540608 T>C maps to NM_000595.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:31540608 T>C maps to NM_000595.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:34003984 G>A maps to NM_000841.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:34003984 G>A maps to NM_000841.1 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:129663556 G>T maps to NM_000426.3 G1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr6:129663556 G>T maps to NM_000426.3 G1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr8:38005843 A>G maps to NM_000349.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr8:38005843 A>G maps to NM_000349.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr9:21141107 C>G maps to NM_002177.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr9:21141107 C>G maps to NM_002177.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr9:116811981 G>T maps to ENST00000374126 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr9:116811981 G>T maps to ENST00000374126 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr9:119204774 G>T maps to ENST00000313400 T1185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chr9:119204774 G>T maps to ENST00000313400 T1185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chrX:35820798 A>G maps to ENST00000422348 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chrX:35820798 A>G maps to ENST00000422348 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chrX:48458764 C>T maps to NM_017883.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chrX:48458764 C>T maps to NM_017883.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chrX:76875915 G>C maps to NM_000489.3 S1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2521-01A-01D-1494-08 chrX:76875915 G>C maps to NM_000489.3 S1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr1:152187662 G>A maps to NM_001009931.1 R2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr1:152187662 G>A maps to NM_001009931.1 R2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr1:167097484 C>A maps to NM_001080426.1 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr1:167097484 C>A maps to NM_001080426.1 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr1:210001492 G>T maps to NM_014388.6 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr1:210001492 G>T maps to NM_014388.6 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr10:102987488 C>T maps to NM_006562.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr10:102987488 C>T maps to NM_006562.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr15:34653630 C>T maps to NM_153613.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr15:34653630 C>T maps to NM_153613.2 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr15:68612684 G>A maps to ENST00000423218 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr15:68612684 G>A maps to ENST00000423218 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr16:30976385 T>C maps to NM_014712.1 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr16:30976385 T>C maps to NM_014712.1 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr18:60021765 G>A maps to NM_003839.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr18:60021765 G>A maps to NM_003839.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr19:8962002 G>A maps to NM_024690.2 I14458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr19:8962002 G>A maps to NM_024690.2 I14458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr2:128944330 G>A maps to NM_020120.3 W1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr2:128944330 G>A maps to NM_020120.3 W1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr21:46000293 C>T maps to NM_198694.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr21:46000293 C>T maps to NM_198694.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr3:45801399 G>A maps to NM_020208.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr3:45801399 G>A maps to NM_020208.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr4:20543201 C>T maps to ENST00000273739 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr4:20543201 C>T maps to ENST00000273739 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr4:151170829 C>G maps to NM_001040261.4 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr4:151170829 C>G maps to NM_001040261.4 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr7:23023599 G>T maps to NM_032581.3 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chr7:23023599 G>T maps to NM_032581.3 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chrX:151820043 C>T maps to NM_018558.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2523-01A-01D-1494-08 chrX:151820043 C>T maps to NM_018558.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr1:6639226 A>G maps to NM_138697.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr1:6639226 A>G maps to NM_138697.3 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr1:109553698 T>A maps to NM_001142550.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr1:109553698 T>A maps to NM_001142550.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr1:152127650 G>A maps to NM_001122965.1 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr1:152127650 G>A maps to NM_001122965.1 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr11:5510784 C>G maps to NM_001005163.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr11:5510784 C>G maps to NM_001005163.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:15073952 G>A maps to NM_152321.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:15073952 G>A maps to NM_152321.2 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:21175883 T>C maps to ENST00000381541 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:21175883 T>C maps to ENST00000381541 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:109052585 G>C maps to ENST00000420959 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:109052585 G>C maps to ENST00000420959 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:110226432 G>A maps to NM_021625.4 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr12:110226432 G>A maps to NM_021625.4 C660C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr13:48951052 G>C did not map to a codon.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr13:48951052 G>C did not map to a codon.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr16:20380897 G>A maps to NM_174924.1 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr16:20380897 G>A maps to NM_174924.1 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr17:12847455 C>T maps to NM_014859.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr17:12847455 C>T maps to NM_014859.4 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr17:42882258 G>T maps to NM_001080383.1 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr17:42882258 G>T maps to NM_001080383.1 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr2:190660524 C>T maps to NM_000534.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr2:190660524 C>T maps to NM_000534.4 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr2:207530694 G>A maps to NM_001093730.1 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr2:207530694 G>A maps to NM_001093730.1 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr2:233632951 A>G maps to NM_002242.4 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr2:233632951 A>G maps to NM_002242.4 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr20:1616836 G>A maps to NM_018556.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr20:1616836 G>A maps to NM_018556.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr20:37356105 G>C maps to NM_080552.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr20:37356105 G>C maps to NM_080552.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr20:61288141 C>T maps to NM_016354.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr20:61288141 C>T maps to NM_016354.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr22:37769171 G>A maps to NM_052906.3 D801D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr22:37769171 G>A maps to NM_052906.3 D801D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr4:139100425 C>A maps to ENST00000280612 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr4:139100425 C>A maps to ENST00000280612 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr7:82584286 T>C maps to NM_033026.5 R1994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr7:82584286 T>C maps to NM_033026.5 R1994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr7:100852148 T>C maps to NM_001084.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr7:100852148 T>C maps to NM_001084.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr7:142609824 A>G maps to NM_019841.4 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chr7:142609824 A>G maps to NM_019841.4 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chrX:53455348 G>A maps to NM_001031745.1 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chrX:53455348 G>A maps to NM_001031745.1 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chrX:134947909 G>A maps to NM_001172288.1 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2524-01A-01D-1494-08 chrX:134947909 G>A maps to NM_001172288.1 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr1:157804374 T>C maps to NM_005894.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr1:157804374 T>C maps to NM_005894.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr12:59271191 A>G maps to NM_153377.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr12:59271191 A>G maps to NM_153377.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr13:20625721 T>C maps to NM_001190965.1 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr13:20625721 T>C maps to NM_001190965.1 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr14:88416242 G>T maps to NM_000153.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr14:88416242 G>T maps to NM_000153.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr15:99251007 G>A maps to NM_000875.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr15:99251007 G>A maps to NM_000875.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr20:58471553 A>G maps to NM_014258.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr20:58471553 A>G maps to NM_014258.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr3:112546469 T>C maps to NM_001008784.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr3:112546469 T>C maps to NM_001008784.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr3:196230194 C>T did not map to a codon.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr3:196230194 C>T did not map to a codon.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr4:40439839 G>A maps to NM_001098634.1 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr4:40439839 G>A maps to NM_001098634.1 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr5:41186198 C>T maps to NM_001115131.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr5:41186198 C>T maps to NM_001115131.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr5:140554314 C>T maps to NM_018940.2 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr5:140554314 C>T maps to NM_018940.2 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr5:160761757 C>T did not map to a codon.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr5:160761757 C>T did not map to a codon.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr6:38750808 C>T maps to ENST00000327475 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr6:38750808 C>T maps to ENST00000327475 D751D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr7:107745022 C>T maps to NM_007356.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr7:107745022 C>T maps to NM_007356.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr8:113420590 G>T maps to NM_198123.1 S1854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chr8:113420590 G>T maps to NM_198123.1 S1854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chrX:47509843 G>A did not map to a codon.
Sequencing variant TCGA-27-2526-01A-01D-1494-08 chrX:47509843 G>A did not map to a codon.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr1:19181420 C>T maps to NM_152232.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr1:19181420 C>T maps to NM_152232.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr1:32126215 G>T maps to NM_001856.3 P1283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr1:32126215 G>T maps to NM_001856.3 P1283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr1:247752158 C>T maps to NM_001001915.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr1:247752158 C>T maps to NM_001001915.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr11:18309167 C>T maps to NM_181507.1 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr11:18309167 C>T maps to NM_181507.1 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr15:42168353 G>A maps to ENST00000320955 S1360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr15:42168353 G>A maps to ENST00000320955 S1360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr15:81628947 A>G maps to ENST00000454937 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr15:81628947 A>G maps to ENST00000454937 G735G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr17:40092756 G>A maps to ENST00000377543 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr17:40092756 G>A maps to ENST00000377543 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr19:44130438 T>C maps to NM_145296.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr19:44130438 T>C maps to NM_145296.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr19:46124851 G>A maps to NM_001193268.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr19:46124851 G>A maps to NM_001193268.1 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr19:58967237 C>T maps to NM_207395.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr19:58967237 C>T maps to NM_207395.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr2:242573478 G>A maps to NM_015963.5 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr2:242573478 G>A maps to NM_015963.5 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr3:14862950 C>A maps to NM_152536.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr3:14862950 C>A maps to NM_152536.3 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr3:39229283 C>T maps to NM_194293.2 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr3:39229283 C>T maps to NM_194293.2 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr3:49062152 G>A maps to NM_000884.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr3:49062152 G>A maps to NM_000884.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr6:31830505 C>T maps to NM_000434.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr6:31830505 C>T maps to NM_000434.3 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr6:51751971 C>T maps to NM_138694.3 P2356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr6:51751971 C>T maps to NM_138694.3 P2356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr6:88170825 G>A maps to NM_001031743.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr6:88170825 G>A maps to NM_001031743.2 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr7:42004152 G>A maps to NM_000168.5 F1506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chr7:42004152 G>A maps to NM_000168.5 F1506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chrX:150349758 C>T maps to NM_004224.3 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2527-01A-01D-1494-08 chrX:150349758 C>T maps to NM_004224.3 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr1:26691222 G>A maps to ENST00000436292 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr1:26691222 G>A maps to ENST00000436292 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr1:228468435 C>T maps to NM_001098623.1 D2712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr1:228468435 C>T maps to NM_001098623.1 D2712D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr11:32413577 G>A maps to NM_024426.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr11:32413577 G>A maps to NM_024426.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr12:2975657 G>A maps to NM_202002.1 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr12:2975657 G>A maps to NM_202002.1 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr12:8376153 C>T did not map to a codon.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr12:8376153 C>T did not map to a codon.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr16:12798556 G>A maps to NM_018340.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr16:12798556 G>A maps to NM_018340.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr17:65889571 T>C maps to ENST00000321892 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr17:65889571 T>C maps to ENST00000321892 F840F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr18:28736073 G>A maps to NM_024421.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr18:28736073 G>A maps to NM_024421.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr18:61585272 C>T maps to NM_005024.1 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr18:61585272 C>T maps to NM_005024.1 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr20:61386134 C>T maps to NM_002531.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr20:61386134 C>T maps to NM_002531.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr3:39126185 T>G maps to NM_020839.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr3:39126185 T>G maps to NM_020839.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr4:48037777 G>A maps to NM_207330.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr4:48037777 G>A maps to NM_207330.1 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr5:36035913 G>A maps to NM_174914.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr5:36035913 G>A maps to NM_174914.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr5:140516911 C>T maps to NM_015669.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-27-2528-01A-01D-1494-08 chr5:140516911 C>T maps to NM_015669.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr1:114454355 G>A maps to NM_022836.3 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr1:114454355 G>A maps to NM_022836.3 W381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr1:186120828 C>A maps to NM_031935.2 L4950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr1:186120828 C>A maps to NM_031935.2 L4950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr15:45555358 G>A maps to NM_004212.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr15:45555358 G>A maps to NM_004212.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr16:10273878 G>A maps to NM_000833.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr16:10273878 G>A maps to NM_000833.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr19:52868954 G>A maps to NM_001161425.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr19:52868954 G>A maps to NM_001161425.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr2:18766136 C>T maps to ENST00000455492 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr2:18766136 C>T maps to ENST00000455492 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:80643624 C>T maps to NM_130767.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:80643624 C>T maps to NM_130767.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:95735873 G>A maps to NM_000439.4 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:95735873 G>A maps to NM_000439.4 R405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:140230083 G>A maps to NM_031857.1 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:140230083 G>A maps to NM_031857.1 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:140811312 G>A maps to NM_003735.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr5:140811312 G>A maps to NM_003735.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr8:133925394 C>T maps to NM_003235.4 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1747-01C-01D-1494-08 chr8:133925394 C>T maps to NM_003235.4 T1421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:17296755 G>A maps to NM_014675.3 R1820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:17296755 G>A maps to NM_014675.3 R1820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:32086484 C>T maps to NM_001525.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:32086484 C>T maps to NM_001525.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:47606459 C>T maps to NM_001010969.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:47606459 C>T maps to NM_001010969.2 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:161682004 C>T maps to NM_001184866.1 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr1:161682004 C>T maps to NM_001184866.1 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr10:89720856 C>A maps to NM_000314.4 Y336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr10:89720856 C>A maps to NM_000314.4 Y336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr15:51031879 A>G maps to NM_032802.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr15:51031879 A>G maps to NM_032802.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr15:71128744 G>A maps to NM_018357.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr15:71128744 G>A maps to NM_018357.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr2:220342015 C>T maps to NM_005876.4 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr2:220342015 C>T maps to NM_005876.4 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr21:10951336 C>T maps to NM_199261.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr21:10951336 C>T maps to NM_199261.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr21:31986019 G>T maps to NM_181602.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr21:31986019 G>T maps to NM_181602.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr21:47957152 C>T maps to ENST00000318711 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr21:47957152 C>T maps to ENST00000318711 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr22:24582098 G>A maps to NM_019601.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr22:24582098 G>A maps to NM_019601.3 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr5:161580199 C>T maps to NM_198903.2 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr5:161580199 C>T maps to NM_198903.2 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr6:117232120 G>A maps to NM_173560.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr6:117232120 G>A maps to NM_173560.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr7:80300316 C>T maps to NM_001127444.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr7:80300316 C>T maps to NM_001127444.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr7:115892025 C>T maps to NM_015641.2 D305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr7:115892025 C>T maps to NM_015641.2 D305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr8:25225731 C>T maps to NM_024940.6 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chr8:25225731 C>T maps to NM_024940.6 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chrX:37668842 T>C maps to NM_000397.3 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-1753-01A-01D-1494-08 chrX:37668842 T>C maps to NM_000397.3 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr11:92531785 C>T maps to ENST00000298047 V1869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr11:92531785 C>T maps to ENST00000298047 V1869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr12:5908716 C>T maps to ENST00000356134 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr12:5908716 C>T maps to ENST00000356134 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr15:63063320 C>T maps to NM_015059.2 G1785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr15:63063320 C>T maps to NM_015059.2 G1785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr19:13050870 C>T maps to NM_004343.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr19:13050870 C>T maps to NM_004343.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr20:43559260 T>A maps to NM_001124756.1 L378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr20:43559260 T>A maps to NM_001124756.1 L378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr4:47886361 C>T did not map to a codon.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr4:47886361 C>T did not map to a codon.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr8:32599523 A>G did not map to a codon.
Sequencing variant TCGA-28-2499-01A-01D-1494-08 chr8:32599523 A>G did not map to a codon.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr1:41514521 G>A maps to NM_001031694.2 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr1:41514521 G>A maps to NM_001031694.2 H372H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr1:155264052 C>T maps to ENST00000423816 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr1:155264052 C>T maps to ENST00000423816 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr10:26465746 C>T maps to NM_017433.4 R1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr10:26465746 C>T maps to NM_017433.4 R1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr11:55606358 T>C maps to NM_001005496.1 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr11:55606358 T>C maps to NM_001005496.1 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr11:76372492 C>T maps to NM_001128922.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr11:76372492 C>T maps to NM_001128922.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr14:21897193 G>A maps to NM_001170629.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr14:21897193 G>A maps to NM_001170629.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr15:43499514 C>T maps to NM_000119.2 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr15:43499514 C>T maps to NM_000119.2 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr15:75198689 C>T maps to NM_020447.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr15:75198689 C>T maps to NM_020447.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr17:72521998 C>T maps to NM_174892.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr17:72521998 C>T maps to NM_174892.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr17:77073796 G>T maps to NM_001042573.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr17:77073796 G>T maps to NM_001042573.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr21:45948428 C>T maps to ENST00000443468 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr21:45948428 C>T maps to ENST00000443468 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr3:134851748 C>A maps to NM_004441.4 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr3:134851748 C>A maps to NM_004441.4 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr3:183824081 G>A maps to NM_182589.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr3:183824081 G>A maps to NM_182589.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr3:197238912 C>T maps to NM_203315.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr3:197238912 C>T maps to NM_203315.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr4:71472353 G>A maps to NM_016519.4 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr4:71472353 G>A maps to NM_016519.4 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr5:148617051 G>T maps to NM_014945.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr5:148617051 G>T maps to NM_014945.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr7:33397474 C>T maps to NM_198428.2 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr7:33397474 C>T maps to NM_198428.2 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr7:86815171 A>G maps to NM_021145.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr7:86815171 A>G maps to NM_021145.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr9:404946 G>A maps to NM_203447.3 T1088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr9:404946 G>A maps to NM_203447.3 T1088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr9:101533298 G>A maps to ENST00000375018 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2501-01A-01D-1696-08 chr9:101533298 G>A maps to ENST00000375018 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr1:85331473 G>A maps to NM_012152.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr1:85331473 G>A maps to NM_012152.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr10:101835787 C>T maps to NM_001308.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr10:101835787 C>T maps to NM_001308.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr12:416883 C>T maps to NM_001042603.1 R1222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr12:416883 C>T maps to NM_001042603.1 R1222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr14:60938272 G>A maps to NM_174978.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr14:60938272 G>A maps to NM_174978.2 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr15:33855070 C>T maps to NM_001036.3 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr15:33855070 C>T maps to NM_001036.3 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr17:67212488 C>A maps to NM_080282.3 G181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr17:67212488 C>A maps to NM_080282.3 G181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr17:68128848 G>A maps to NM_018658.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr17:68128848 G>A maps to NM_018658.1 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:2877813 G>A maps to NM_024967.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:2877813 G>A maps to NM_024967.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:15132709 G>A maps to NM_173482.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:15132709 G>A maps to NM_173482.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:35940985 C>T maps to NM_005306.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:35940985 C>T maps to NM_005306.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:39098514 G>A maps to NM_001042600.1 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:39098514 G>A maps to NM_001042600.1 D382D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:46275973 C>T maps to NM_004409.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr19:46275973 C>T maps to NM_004409.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr22:32828359 G>A maps to NM_174932.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr22:32828359 G>A maps to NM_174932.2 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr22:36696180 G>A maps to NM_002473.4 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr22:36696180 G>A maps to NM_002473.4 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr22:50617531 C>T maps to NM_052839.3 N620N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr22:50617531 C>T maps to NM_052839.3 N620N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr3:100365558 T>C maps to NM_032787.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr3:100365558 T>C maps to NM_032787.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr3:122003131 C>T maps to NM_001178065.1 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr3:122003131 C>T maps to NM_001178065.1 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr5:71490831 A>G maps to NM_005909.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr5:71490831 A>G maps to NM_005909.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr6:31474136 C>T maps to NM_005931.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr6:31474136 C>T maps to NM_005931.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr7:63727108 T>A maps to NM_153363.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr7:63727108 T>A maps to NM_153363.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr7:100696359 C>T maps to NM_001040105.1 V4399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr7:100696359 C>T maps to NM_001040105.1 V4399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr7:144098529 G>A maps to ENST00000467773 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chr7:144098529 G>A maps to ENST00000467773 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chrX:34962108 G>A maps to NM_152631.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2502-01B-01D-1494-08 chrX:34962108 G>A maps to NM_152631.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr1:228529315 G>A did not map to a codon.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr1:228529315 G>A did not map to a codon.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr11:62400734 C>T maps to NM_198335.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr11:62400734 C>T maps to NM_198335.2 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr11:125788548 C>T maps to NM_013264.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr11:125788548 C>T maps to NM_013264.3 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr12:70928633 G>A maps to NM_001109754.1 I2061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr12:70928633 G>A maps to NM_001109754.1 I2061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr12:113737740 G>A maps to NM_024959.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr12:113737740 G>A maps to NM_024959.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr14:93022209 G>A maps to NM_024832.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr14:93022209 G>A maps to NM_024832.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr15:30053399 G>A maps to NM_003257.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr15:30053399 G>A maps to NM_003257.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr15:76196837 C>T maps to NM_147188.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr15:76196837 C>T maps to NM_147188.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr16:3458789 G>A maps to NM_003450.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr16:3458789 G>A maps to NM_003450.2 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr19:5776308 C>T maps to NM_152784.3 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr19:5776308 C>T maps to NM_152784.3 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr19:9090863 G>A maps to NM_024690.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr19:9090863 G>A maps to NM_024690.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr2:166611229 G>A maps to NM_004482.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr2:166611229 G>A maps to NM_004482.3 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr2:180014057 C>A maps to NM_178123.4 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr2:180014057 C>A maps to NM_178123.4 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr5:150639410 C>T maps to NM_000405.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr5:150639410 C>T maps to NM_000405.4 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr6:157495208 C>T maps to ENST00000367148 D1018D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr6:157495208 C>T maps to ENST00000367148 D1018D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr7:127222985 A>G maps to NM_024523.5 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr7:127222985 A>G maps to NM_024523.5 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr8:143425639 G>A maps to ENST00000445818 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chr8:143425639 G>A maps to ENST00000445818 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:26212631 G>A maps to NM_173523.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:26212631 G>A maps to NM_173523.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:107084128 C>T maps to NM_012216.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:107084128 C>T maps to NM_012216.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:130416633 G>A maps to NM_001170961.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:130416633 G>A maps to NM_001170961.1 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:134655170 C>T maps to NM_182540.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2509-01A-01D-1494-08 chrX:134655170 C>T maps to NM_182540.4 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr11:58318639 C>T maps to NM_004811.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr11:58318639 C>T maps to NM_004811.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr12:111748208 C>T maps to NM_015267.3 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr12:111748208 C>T maps to NM_015267.3 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr14:52507432 G>A maps to NM_007361.3 Y654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr14:52507432 G>A maps to NM_007361.3 Y654Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr14:73578302 T>C maps to NM_021239.2 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr14:73578302 T>C maps to NM_021239.2 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr16:12220511 G>A maps to NM_001080530.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr16:12220511 G>A maps to NM_001080530.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr18:19997765 G>A maps to NM_172241.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr18:19997765 G>A maps to NM_172241.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr19:56372799 C>A maps to NM_134444.4 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr19:56372799 C>A maps to NM_134444.4 T635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr2:179633436 A>G maps to NM_133378.4 A3042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chr2:179633436 A>G maps to NM_133378.4 A3042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chrX:18195710 C>T maps to NM_153346.4 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2510-01A-01D-1696-08 chrX:18195710 C>T maps to NM_153346.4 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr1:152275655 G>A maps to NM_002016.1 P3902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr1:152275655 G>A maps to NM_002016.1 P3902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr1:152329435 G>A maps to NM_001014342.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr1:152329435 G>A maps to NM_001014342.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr10:89693008 G>T did not map to a codon.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr10:89693008 G>T did not map to a codon.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr12:132512815 G>A maps to ENST00000333577 L1824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr12:132512815 G>A maps to ENST00000333577 L1824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr16:339598 G>T maps to NM_003502.3 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr16:339598 G>T maps to NM_003502.3 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr16:31308872 C>T maps to NM_001145808.1 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr16:31308872 C>T maps to NM_001145808.1 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr16:72821853 C>A maps to NM_006885.3 E3441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr16:72821853 C>A maps to NM_006885.3 E3441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr18:18547744 T>A maps to NM_005406.2 K1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr18:18547744 T>A maps to NM_005406.2 K1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr18:28673540 G>A maps to ENST00000438199 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr18:28673540 G>A maps to ENST00000438199 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr19:56614550 C>T maps to NM_001002836.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr19:56614550 C>T maps to NM_001002836.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr2:50765580 G>A maps to ENST00000404971 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr2:50765580 G>A maps to ENST00000404971 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr3:123333122 G>A maps to NM_053025.3 D1858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr3:123333122 G>A maps to NM_053025.3 D1858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr3:183665138 C>A maps to NM_005688.2 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr3:183665138 C>A maps to NM_005688.2 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr3:184044340 G>A maps to NM_001194947.1 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr3:184044340 G>A maps to NM_001194947.1 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr4:7043695 C>A maps to NM_153376.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr4:7043695 C>A maps to NM_153376.2 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr5:94288920 A>G did not map to a codon.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr5:94288920 A>G did not map to a codon.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr7:149427521 G>A maps to NM_032534.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr7:149427521 G>A maps to NM_032534.2 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr8:59512580 C>T did not map to a codon.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr8:59512580 C>T did not map to a codon.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr8:110497283 G>A maps to ENST00000426474 E3196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chr8:110497283 G>A maps to ENST00000426474 E3196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chrX:72667160 C>T maps to NM_005193.1 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2513-01A-01D-1494-08 chrX:72667160 C>T maps to NM_005193.1 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr13:24448984 C>T maps to NM_005932.3 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr13:24448984 C>T maps to NM_005932.3 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr13:103520595 C>T maps to NM_000123.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr13:103520595 C>T maps to NM_000123.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr16:2156264 G>A maps to NM_001009944.2 Y2510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr16:2156264 G>A maps to NM_001009944.2 Y2510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr16:4755094 C>T did not map to a codon.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr16:4755094 C>T did not map to a codon.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:3293344 C>T maps to NM_021938.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:3293344 C>T maps to NM_021938.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:6665272 G>A maps to NM_003807.3 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:6665272 G>A maps to NM_003807.3 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:7964175 C>T maps to NM_025061.3 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:7964175 C>T maps to NM_025061.3 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:11221367 C>T maps to NM_000527.4 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:11221367 C>T maps to NM_000527.4 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:43359719 C>G did not map to a codon.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:43359719 C>G did not map to a codon.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:55495081 C>T maps to NM_017852.3 D672D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:55495081 C>T maps to NM_017852.3 D672D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:55693401 C>T maps to NM_002842.3 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr19:55693401 C>T maps to NM_002842.3 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr2:103095610 C>T maps to NM_001011552.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr2:103095610 C>T maps to NM_001011552.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr3:108549620 C>T maps to NM_016388.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr3:108549620 C>T maps to NM_016388.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr3:160083929 C>T maps to ENST00000483754 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr3:160083929 C>T maps to ENST00000483754 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr4:109667552 A>G did not map to a codon.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr4:109667552 A>G did not map to a codon.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr4:119948016 C>T maps to NM_133477.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr4:119948016 C>T maps to NM_133477.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr5:140553288 G>T maps to NM_018940.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr5:140553288 G>T maps to NM_018940.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr6:167360226 C>T maps to ENST00000428859 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr6:167360226 C>T maps to ENST00000428859 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr7:48443393 C>T maps to NM_152701.3 T3996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr7:48443393 C>T maps to NM_152701.3 T3996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr9:112686090 C>T maps to NM_007203.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-2514-01A-02D-1494-08 chr9:112686090 C>T maps to NM_007203.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr11:50003719 A>G maps to NM_001005270.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr11:50003719 A>G maps to NM_001005270.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr13:72053351 C>A maps to ENST00000359684 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr13:72053351 C>A maps to ENST00000359684 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr15:89400786 A>T maps to NM_013227.3 P1657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr15:89400786 A>T maps to NM_013227.3 P1657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr17:76083172 C>T maps to NM_001142640.1 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr17:76083172 C>T maps to NM_001142640.1 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr19:59067681 C>T did not map to a codon.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr19:59067681 C>T did not map to a codon.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr2:113532646 C>T maps to NM_000575.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr2:113532646 C>T maps to NM_000575.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr2:179448472 G>A maps to NM_133378.4 H19244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr2:179448472 G>A maps to NM_133378.4 H19244H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr3:14197914 C>T maps to NM_004628.4 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr3:14197914 C>T maps to NM_004628.4 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr4:78665958 G>A maps to ENST00000512485 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr4:78665958 G>A maps to ENST00000512485 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr5:96239219 T>C maps to NM_001130140.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr5:96239219 T>C maps to NM_001130140.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chrX:107977901 G>T maps to NM_003604.2 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5204-01A-01D-1486-08 chrX:107977901 G>T maps to NM_003604.2 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr1:157740304 A>T maps to NM_030764.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr1:157740304 A>T maps to NM_030764.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr1:186099744 G>A maps to NM_031935.2 Q4382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr1:186099744 G>A maps to NM_031935.2 Q4382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr1:197062331 G>C maps to NM_018136.4 V3048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr1:197062331 G>C maps to NM_018136.4 V3048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr10:21124443 C>A maps to ENST00000430741 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr10:21124443 C>A maps to ENST00000430741 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr10:105798221 C>A maps to NM_000494.3 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr10:105798221 C>A maps to NM_000494.3 P1004P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr11:74904383 G>A maps to NM_007256.4 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr11:74904383 G>A maps to NM_007256.4 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr17:45925366 G>A maps to NM_199262.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr17:45925366 G>A maps to NM_199262.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr17:72926422 C>T maps to NM_178160.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr17:72926422 C>T maps to NM_178160.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr19:10394790 C>T maps to NM_000201.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr19:10394790 C>T maps to NM_000201.2 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr19:35449588 G>A maps to NM_175872.4 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr19:35449588 G>A maps to NM_175872.4 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr19:40360854 C>A did not map to a codon.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr19:40360854 C>A did not map to a codon.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:46987000 G>T maps to NM_144949.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:46987000 G>T maps to NM_144949.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:136558293 G>A maps to NM_002299.2 N1583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:136558293 G>A maps to NM_002299.2 N1583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:144381720 C>T maps to NM_018460.3 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:144381720 C>T maps to NM_018460.3 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:179647000 G>A maps to NM_133378.4 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr2:179647000 G>A maps to NM_133378.4 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr5:141694229 G>A maps to NM_030964.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr5:141694229 G>A maps to NM_030964.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr6:32974897 G>A maps to NM_002119.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr6:32974897 G>A maps to NM_002119.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr6:46678391 G>T maps to NM_001168357.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr6:46678391 G>T maps to NM_001168357.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr7:131859665 C>T maps to NM_020911.1 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr7:131859665 C>T maps to NM_020911.1 L1296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr8:144690264 A>G maps to NM_023078.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5207-01A-01D-1486-08 chr8:144690264 A>G maps to NM_023078.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr1:152484250 C>T maps to NM_178438.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr1:152484250 C>T maps to NM_178438.4 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:197576 G>A maps to NM_053280.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:197576 G>A maps to NM_053280.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:55606712 G>A maps to NM_001005496.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:55606712 G>A maps to NM_001005496.1 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:62284307 G>A maps to NM_001620.1 R5861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:62284307 G>A maps to NM_001620.1 R5861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:120983845 C>T maps to NM_005422.2 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr11:120983845 C>T maps to NM_005422.2 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr14:81610024 C>T maps to NM_000369.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr14:81610024 C>T maps to NM_000369.2 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr15:42058283 C>T maps to ENST00000219905 G2717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr15:42058283 C>T maps to ENST00000219905 G2717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr17:29533377 C>T maps to NM_001042492.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr17:29533377 C>T maps to NM_001042492.2 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr17:43333266 G>A maps to NM_152343.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr17:43333266 G>A maps to NM_152343.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr2:233274392 C>T maps to NM_031313.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr2:233274392 C>T maps to NM_031313.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr20:62571757 C>T maps to NM_017859.3 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr20:62571757 C>T maps to NM_017859.3 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr21:10942994 G>A maps to NM_199261.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr21:10942994 G>A maps to NM_199261.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr3:52014463 G>A maps to NM_015407.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr3:52014463 G>A maps to NM_015407.4 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr5:140167728 G>A maps to NM_018900.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr5:140167728 G>A maps to NM_018900.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr5:140590287 G>A maps to NM_018932.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr5:140590287 G>A maps to NM_018932.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr5:140736434 C>T maps to NM_018917.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr5:140736434 C>T maps to NM_018917.2 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr7:92763757 A>C maps to NM_152703.2 Y509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr7:92763757 A>C maps to NM_152703.2 Y509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr9:32784669 C>T maps to NM_212558.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chr9:32784669 C>T maps to NM_212558.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chrX:109922645 G>A maps to NM_001143981.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5208-01A-01D-1486-08 chrX:109922645 G>A maps to NM_001143981.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr10:103190196 C>T maps to NM_033637.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr10:103190196 C>T maps to NM_033637.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr11:60531220 C>T maps to NM_001098835.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr11:60531220 C>T maps to NM_001098835.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:49164591 C>T maps to NM_015270.3 K1071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:49164591 C>T maps to NM_015270.3 K1071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:49221582 G>A maps to NM_000725.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:49221582 G>A maps to NM_000725.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:93792555 C>T maps to NM_199040.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:93792555 C>T maps to NM_199040.2 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:107371335 C>T maps to NM_025198.3 *386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr12:107371335 C>T maps to NM_025198.3 *386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr15:44858194 G>A maps to NM_025137.3 R2286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr15:44858194 G>A maps to NM_025137.3 R2286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr18:12351332 C>T maps to NM_006796.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr18:12351332 C>T maps to NM_006796.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:10394190 C>T maps to NM_000201.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:10394190 C>T maps to NM_000201.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:14865774 G>A maps to NM_013447.2 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:14865774 G>A maps to NM_013447.2 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:22575721 T>C maps to NM_001098626.1 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:22575721 T>C maps to NM_001098626.1 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:33585092 C>T maps to NM_018025.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr19:33585092 C>T maps to NM_018025.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr2:179631233 G>A maps to NM_133378.4 R3193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr2:179631233 G>A maps to NM_133378.4 R3193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr20:17434532 C>T maps to NM_002594.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr20:17434532 C>T maps to NM_002594.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr21:46320315 G>A maps to NM_000211.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr21:46320315 G>A maps to NM_000211.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr22:51008724 G>A maps to NM_152245.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr22:51008724 G>A maps to NM_152245.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr3:53837548 T>G maps to NM_001128840.1 Y1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr3:53837548 T>G maps to NM_001128840.1 Y1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr4:89053762 G>A maps to NM_004827.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr4:89053762 G>A maps to NM_004827.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr4:96762204 C>T maps to NM_005390.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr4:96762204 C>T maps to NM_005390.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr6:158483052 C>T maps to NM_003898.3 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr6:158483052 C>T maps to NM_003898.3 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:31682504 G>A maps to NM_194300.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:31682504 G>A maps to NM_194300.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:44146385 G>A maps to NM_001129.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:44146385 G>A maps to NM_001129.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:55268063 C>T maps to NM_005228.3 F968F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:55268063 C>T maps to NM_005228.3 F968F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:55268066 C>G maps to NM_005228.3 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:55268066 C>G maps to NM_005228.3 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:83032081 G>A maps to NM_012431.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:83032081 G>A maps to NM_012431.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:101926059 C>T maps to NM_001913.2 C653C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chr7:101926059 C>T maps to NM_001913.2 C653C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:30268849 C>T maps to NM_177404.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:30268849 C>T maps to NM_177404.2 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:48564986 C>T maps to NM_003173.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:48564986 C>T maps to NM_003173.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:78427064 C>A maps to NM_032553.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:78427064 C>A maps to NM_032553.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:153032872 G>A maps to NM_005393.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5209-01A-01D-1486-08 chrX:153032872 G>A maps to NM_005393.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr1:216595381 G>A maps to ENST00000366943 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr1:216595381 G>A maps to ENST00000366943 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr1:247752221 C>A maps to NM_001001915.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr1:247752221 C>A maps to NM_001001915.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr10:122622304 A>G maps to NM_018117.11 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr10:122622304 A>G maps to NM_018117.11 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr14:64497732 G>A did not map to a codon.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr14:64497732 G>A did not map to a codon.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr15:35045226 G>A maps to NM_020660.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr15:35045226 G>A maps to NM_020660.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr17:9792805 G>A maps to NM_004246.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr17:9792805 G>A maps to NM_004246.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr17:39633980 A>G maps to NM_002280.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr17:39633980 A>G maps to NM_002280.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr2:75720532 G>A maps to NM_032181.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr2:75720532 G>A maps to NM_032181.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr6:20402624 G>C maps to NM_001949.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr6:20402624 G>C maps to NM_001949.3 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr8:12957580 C>T maps to NM_182643.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr8:12957580 C>T maps to NM_182643.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr9:130670778 C>T maps to NM_175039.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5211-01C-11D-1845-08 chr9:130670778 C>T maps to NM_175039.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:18808935 G>A maps to NM_152375.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:18808935 G>A maps to NM_152375.2 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:38079484 G>A maps to NM_001038633.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:38079484 G>A maps to NM_001038633.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:62253475 C>T maps to NM_176877.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:62253475 C>T maps to NM_176877.2 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:117663349 G>A maps to NM_025188.3 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr1:117663349 G>A maps to NM_025188.3 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:12278417 G>A maps to NM_014632.2 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:12278417 G>A maps to NM_014632.2 R1014R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:62396738 G>A maps to NM_198335.2 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:62396738 G>A maps to NM_198335.2 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:65628470 C>T maps to NM_025128.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:65628470 C>T maps to NM_025128.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:74800716 G>A maps to NM_001005285.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:74800716 G>A maps to NM_001005285.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:118375648 A>C maps to NM_001197104.1 S3014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr11:118375648 A>C maps to NM_001197104.1 S3014S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr12:109921387 G>A maps to NM_183415.1 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr12:109921387 G>A maps to NM_183415.1 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr14:95677203 C>T maps to NM_024734.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr14:95677203 C>T maps to NM_024734.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr15:25953146 G>A maps to NM_024490.3 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr15:25953146 G>A maps to NM_024490.3 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr15:44090143 A>G maps to ENST00000319327 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr15:44090143 A>G maps to ENST00000319327 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr17:8158343 G>A did not map to a codon.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr17:8158343 G>A did not map to a codon.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr19:5844199 G>A maps to NM_001097641.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr19:5844199 G>A maps to NM_001097641.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr2:179410766 C>T maps to NM_133378.4 P29164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr2:179410766 C>T maps to NM_133378.4 P29164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr2:208993025 C>T maps to NM_020989.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr2:208993025 C>T maps to NM_020989.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr20:43933303 G>A maps to ENST00000372754 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr20:43933303 G>A maps to ENST00000372754 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr7:48056900 A>G maps to NM_152782.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chr7:48056900 A>G maps to NM_152782.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chrX:30327198 C>T maps to NM_000475.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5213-01A-01D-1486-08 chrX:30327198 C>T maps to NM_000475.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:1256375 G>A maps to NM_017871.4 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:1256375 G>A maps to NM_017871.4 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:5937353 T>C maps to NM_015102.2 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:5937353 T>C maps to NM_015102.2 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:152282615 C>T maps to NM_002016.1 A1582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:152282615 C>T maps to NM_002016.1 A1582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:201289493 C>T maps to NM_000299.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:201289493 C>T maps to NM_000299.3 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:216061962 C>T maps to ENST00000366943 P2676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr1:216061962 C>T maps to ENST00000366943 P2676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr11:65367000 C>A maps to NM_002419.3 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr11:65367000 C>A maps to NM_002419.3 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr15:33359641 A>G maps to NM_001103184.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr15:33359641 A>G maps to NM_001103184.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr15:45709545 A>G maps to NM_024063.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr15:45709545 A>G maps to NM_024063.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr17:26864327 A>C maps to NM_003593.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr17:26864327 A>C maps to NM_003593.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr19:4475291 C>T maps to ENST00000301284 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr19:4475291 C>T maps to ENST00000301284 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr19:55106241 T>C maps to NM_006863.1 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr19:55106241 T>C maps to NM_006863.1 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr2:219503256 G>A maps to NM_001105537.1 C1623C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr2:219503256 G>A maps to NM_001105537.1 C1623C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr20:13279760 C>T maps to NM_080826.1 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr20:13279760 C>T maps to NM_080826.1 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr4:162577554 T>C maps to NM_020116.3 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr4:162577554 T>C maps to NM_020116.3 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr6:12123450 C>T maps to NM_002114.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr6:12123450 C>T maps to NM_002114.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr6:49754387 G>A maps to NM_138733.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr6:49754387 G>A maps to NM_138733.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr7:106509058 C>T maps to NM_002649.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr7:106509058 C>T maps to NM_002649.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr7:142460294 C>T maps to ENST00000486171 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr7:142460294 C>T maps to ENST00000486171 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr8:141310661 T>C maps to NM_031466.5 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr8:141310661 T>C maps to NM_031466.5 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr9:27949564 G>A maps to NM_152570.1 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chr9:27949564 G>A maps to NM_152570.1 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chrX:72667326 C>T maps to NM_005193.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chrX:72667326 C>T maps to NM_005193.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chrX:76918964 C>T maps to NM_000489.3 R1342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chrX:76918964 C>T maps to NM_000489.3 R1342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chrX:149013837 G>A maps to NM_005364.4 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5214-01A-01D-1486-08 chrX:149013837 G>A maps to NM_005364.4 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr1:19451181 A>G maps to ENST00000375267 G3147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr1:19451181 A>G maps to ENST00000375267 G3147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr10:127541112 T>C maps to NM_018180.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr10:127541112 T>C maps to NM_018180.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr11:75852115 G>T maps to NM_003369.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr11:75852115 G>T maps to NM_003369.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr12:50387941 G>C maps to NM_013277.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr12:50387941 G>C maps to NM_013277.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr12:129694160 G>A maps to NM_133448.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr12:129694160 G>A maps to NM_133448.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr14:21109808 G>A maps to NM_001001968.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr14:21109808 G>A maps to NM_001001968.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr16:46615748 C>T maps to NM_024745.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr16:46615748 C>T maps to NM_024745.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr17:10432721 A>T maps to NM_017534.5 L1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr17:10432721 A>T maps to NM_017534.5 L1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr17:38252311 T>C maps to NM_021724.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr17:38252311 T>C maps to NM_021724.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr3:32933301 A>G maps to NM_001039111.1 *869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr3:32933301 A>G maps to NM_001039111.1 *869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr3:164733000 A>G maps to NM_001041.3 N1303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr3:164733000 A>G maps to NM_001041.3 N1303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr4:115998230 G>A did not map to a codon.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr4:115998230 G>A did not map to a codon.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr5:140176552 G>A maps to NM_018905.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr5:140176552 G>A maps to NM_018905.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr6:30164403 C>T maps to NM_003449.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr6:30164403 C>T maps to NM_003449.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr6:100911317 C>T maps to ENST00000262901 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr6:100911317 C>T maps to ENST00000262901 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr6:159655380 G>A maps to NM_032532.2 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr6:159655380 G>A maps to NM_032532.2 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr7:29438048 C>T maps to NM_004067.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr7:29438048 C>T maps to NM_004067.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr7:95115357 A>G maps to NM_016116.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chr7:95115357 A>G maps to NM_016116.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chrX:27765561 C>T maps to NM_001136533.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5215-01A-01D-1486-08 chrX:27765561 C>T maps to NM_001136533.1 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr1:94512563 C>T maps to NM_000350.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr1:94512563 C>T maps to NM_000350.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr10:119014866 C>T maps to NM_003054.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr10:119014866 C>T maps to NM_003054.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr11:60164080 A>T maps to NM_032597.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr11:60164080 A>T maps to NM_032597.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr12:49177052 G>T maps to NM_015270.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr12:49177052 G>T maps to NM_015270.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr12:88505569 A>G maps to NM_025114.3 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr12:88505569 A>G maps to NM_025114.3 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr12:101796695 C>T maps to NM_001177.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr12:101796695 C>T maps to NM_001177.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr13:23911702 C>T maps to NM_014363.4 G2104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr13:23911702 C>T maps to NM_014363.4 G2104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr14:105518248 G>A maps to NM_013345.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr14:105518248 G>A maps to NM_013345.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr15:50935594 A>G maps to NM_017672.4 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr15:50935594 A>G maps to NM_017672.4 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr17:10428376 A>G maps to NM_017534.5 S1556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr17:10428376 A>G maps to NM_017534.5 S1556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr17:66924135 A>T maps to NM_007168.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr17:66924135 A>T maps to NM_007168.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr19:3823273 C>A maps to NM_015174.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr19:3823273 C>A maps to NM_015174.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr19:17013523 G>A maps to ENST00000443236 D1597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr19:17013523 G>A maps to ENST00000443236 D1597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr19:53761867 C>T maps to NM_173856.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr19:53761867 C>T maps to NM_173856.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr20:50408433 C>A maps to NM_020436.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr20:50408433 C>A maps to NM_020436.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr4:175229837 A>G did not map to a codon.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr4:175229837 A>G did not map to a codon.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr8:144992144 C>T maps to NM_201380.2 S4085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5216-01A-01D-1486-08 chr8:144992144 C>T maps to NM_201380.2 S4085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr10:129861344 A>T did not map to a codon.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr10:129861344 A>T did not map to a codon.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr11:64575520 G>A maps to NM_130804.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr11:64575520 G>A maps to NM_130804.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr11:82693314 G>A maps to NM_014488.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr11:82693314 G>A maps to NM_014488.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr12:66698565 G>A maps to NM_033647.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr12:66698565 G>A maps to NM_033647.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr16:30774842 G>A maps to NM_014771.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr16:30774842 G>A maps to NM_014771.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr2:164467615 G>A maps to NM_018086.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr2:164467615 G>A maps to NM_018086.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr3:196613119 G>A maps to NM_152699.4 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr3:196613119 G>A maps to NM_152699.4 W356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr6:29142194 C>G maps to NM_030905.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr6:29142194 C>G maps to NM_030905.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr7:143098436 G>A maps to NM_005232.4 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5218-01A-01D-1486-08 chr7:143098436 G>A maps to NM_005232.4 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr12:111099034 G>A maps to NM_001040107.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr12:111099034 G>A maps to NM_001040107.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr12:123097663 A>G maps to NM_014708.4 L1876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr12:123097663 A>G maps to NM_014708.4 L1876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr17:7579698 C>T did not map to a codon.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr17:7579698 C>T did not map to a codon.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr19:1578434 C>T maps to NM_003926.5 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr19:1578434 C>T maps to NM_003926.5 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr19:15280950 C>T maps to NM_000435.2 G1715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr19:15280950 C>T maps to NM_000435.2 G1715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr19:39398199 C>T maps to NM_002503.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr19:39398199 C>T maps to NM_002503.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr21:43161459 G>A maps to ENST00000352483 N679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr21:43161459 G>A maps to ENST00000352483 N679N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr22:32239091 C>T maps to NM_001136029.1 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr22:32239091 C>T maps to NM_001136029.1 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr3:52551108 C>T maps to NM_015136.2 D1491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr3:52551108 C>T maps to NM_015136.2 D1491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr3:152058531 A>G maps to NM_001123228.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr3:152058531 A>G maps to NM_001123228.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr6:70637866 C>T maps to NM_001858.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr6:70637866 C>T maps to NM_001858.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr7:84671589 T>C maps to NM_152754.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr7:84671589 T>C maps to NM_152754.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr9:39140558 T>A maps to NM_033655.3 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chr9:39140558 T>A maps to NM_033655.3 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chrX:151900251 G>A maps to NM_005367.5 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5219-01A-01D-1486-08 chrX:151900251 G>A maps to NM_005367.5 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr1:43396817 G>A maps to NM_006516.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr1:43396817 G>A maps to NM_006516.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr11:57559036 G>A maps to NM_001085458.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr11:57559036 G>A maps to NM_001085458.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr11:114182997 G>A maps to NM_006169.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr11:114182997 G>A maps to NM_006169.2 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr11:123624635 G>A maps to NM_001005188.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr11:123624635 G>A maps to NM_001005188.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr16:4414381 C>T maps to NM_024535.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr16:4414381 C>T maps to NM_024535.3 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr19:50387770 C>T maps to NM_024682.2 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr19:50387770 C>T maps to NM_024682.2 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr20:36789861 G>A maps to NM_004613.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr20:36789861 G>A maps to NM_004613.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr22:38471060 G>A maps to NM_012407.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr22:38471060 G>A maps to NM_012407.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr8:121219269 C>T maps to NM_021110.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr8:121219269 C>T maps to NM_021110.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr9:79635211 C>T maps to NM_001013735.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-5220-01A-01D-1486-08 chr9:79635211 C>T maps to NM_001013735.1 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr1:6705884 T>C maps to NM_018198.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr1:6705884 T>C maps to NM_018198.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr1:154293714 T>C maps to NM_080429.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr1:154293714 T>C maps to NM_080429.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr13:46718595 G>A maps to NM_002298.4 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr13:46718595 G>A maps to NM_002298.4 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr15:89876415 G>A maps to NM_002693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr15:89876415 G>A maps to NM_002693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr20:44669235 C>T maps to NM_001134771.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr20:44669235 C>T maps to NM_001134771.1 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr3:32180197 G>A maps to NM_015141.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr3:32180197 G>A maps to NM_015141.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr4:2934850 C>T maps to NM_001146069.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr4:2934850 C>T maps to NM_001146069.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr4:175160247 G>C maps to NM_012180.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr4:175160247 G>C maps to NM_012180.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr5:140214001 C>T maps to NM_018910.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr5:140214001 C>T maps to NM_018910.2 R12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr5:140751754 G>A maps to NM_018924.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr5:140751754 G>A maps to NM_018924.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr6:30573988 A>G maps to NM_002714.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr6:30573988 A>G maps to NM_002714.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr8:39781103 C>T maps to NM_002164.4 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chr8:39781103 C>T maps to NM_002164.4 H218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chrX:21675507 G>A maps to NM_153270.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chrX:21675507 G>A maps to NM_153270.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chrX:140967025 G>A maps to NM_138702.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-28-6450-01A-11D-1696-08 chrX:140967025 G>A maps to NM_138702.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:12164491 C>T maps to NM_001243.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:12164491 C>T maps to NM_001243.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:44437536 G>T maps to NM_001384.4 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:44437536 G>T maps to NM_001384.4 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:79002162 C>T maps to NM_000959.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:79002162 C>T maps to NM_000959.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:247654809 C>T maps to NM_001004698.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:247654809 C>T maps to NM_001004698.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:248224639 G>T maps to NM_001004687.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:248224639 G>T maps to NM_001004687.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:248685399 C>T maps to NM_001013355.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr1:248685399 C>T maps to NM_001013355.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr10:96447616 C>T maps to NM_000772.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr10:96447616 C>T maps to NM_000772.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:18158841 G>A maps to NM_054031.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:18158841 G>A maps to NM_054031.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:57982380 C>T maps to NM_001004458.1 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:57982380 C>T maps to NM_001004458.1 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:59837090 C>T maps to NM_006138.4 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:59837090 C>T maps to NM_006138.4 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:92714859 C>A maps to NM_005959.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr11:92714859 C>A maps to NM_005959.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr12:51723539 G>A maps to NM_001971.5 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr12:51723539 G>A maps to NM_001971.5 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr13:49039350 T>A maps to NM_000321.2 L779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr13:49039350 T>A maps to NM_000321.2 L779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr16:57153519 C>T maps to NM_152727.5 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr16:57153519 C>T maps to NM_152727.5 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr17:7220633 G>A maps to NM_032442.2 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr17:7220633 G>A maps to NM_032442.2 F1458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr17:27228287 C>T maps to NM_144683.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr17:27228287 C>T maps to NM_144683.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr19:14785603 C>T did not map to a codon.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr19:14785603 C>T did not map to a codon.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr2:116497459 G>A maps to NM_020868.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr2:116497459 G>A maps to NM_020868.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr2:191765418 G>A maps to NM_014905.3 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr2:191765418 G>A maps to NM_014905.3 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr20:47887009 G>A maps to NM_021035.2 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr20:47887009 G>A maps to NM_021035.2 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr22:24807597 C>T maps to NM_015330.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr22:24807597 C>T maps to NM_015330.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:45942420 G>A maps to NM_031200.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:45942420 G>A maps to NM_031200.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:52540232 G>A maps to NM_015136.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:52540232 G>A maps to NM_015136.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:111852080 G>A did not map to a codon.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:111852080 G>A did not map to a codon.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:168833868 C>T maps to NM_004991.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr3:168833868 C>T maps to NM_004991.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr5:40976858 G>A maps to NM_000587.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr5:40976858 G>A maps to NM_000587.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr5:140730078 C>T maps to NM_018922.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr5:140730078 C>T maps to NM_018922.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr7:40127782 C>T maps to NM_003718.4 Q1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr7:40127782 C>T maps to NM_003718.4 Q1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr7:63680235 C>T maps to NM_001159524.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr7:63680235 C>T maps to NM_001159524.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr7:86468917 C>T maps to NM_000840.2 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr7:86468917 C>T maps to NM_000840.2 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr8:143625026 C>T maps to NM_001702.2 H1505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr8:143625026 C>T maps to NM_001702.2 H1505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr9:107379552 C>T maps to NM_001001956.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1970-01A-01D-1494-08 chr9:107379552 C>T maps to NM_001001956.1 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:19168298 C>T maps to NM_152232.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:19168298 C>T maps to NM_152232.2 K505K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:44069549 G>A maps to NM_002840.3 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:44069549 G>A maps to NM_002840.3 R909R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:68603589 G>A maps to NM_024911.6 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:68603589 G>A maps to NM_024911.6 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:149885275 G>A maps to NM_014849.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:149885275 G>A maps to NM_014849.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:152283083 G>A maps to NM_002016.1 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr1:152283083 G>A maps to NM_002016.1 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr10:50820048 C>T maps to NM_003055.2 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr10:50820048 C>T maps to NM_003055.2 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr10:75849001 T>C maps to NM_014000.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr10:75849001 T>C maps to NM_014000.2 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr10:93619321 C>A maps to NM_025235.3 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr10:93619321 C>A maps to NM_025235.3 S1066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr11:4842971 C>T maps to NM_001004753.1 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr11:4842971 C>T maps to NM_001004753.1 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr11:65402834 G>A maps to NM_032223.2 A1700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr11:65402834 G>A maps to NM_032223.2 A1700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr12:45173690 C>T maps to NM_001145107.1 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr12:45173690 C>T maps to NM_001145107.1 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr12:53242330 C>T maps to NM_173352.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr12:53242330 C>T maps to NM_173352.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr13:76134908 A>T maps to NM_006002.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr13:76134908 A>T maps to NM_006002.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr14:24567813 T>C maps to NM_004563.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr14:24567813 T>C maps to NM_004563.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr14:29237321 C>T maps to NM_005249.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr14:29237321 C>T maps to NM_005249.3 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:1841524 G>A maps to NM_001146006.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:1841524 G>A maps to NM_001146006.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:2903294 G>A maps to NM_022119.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:2903294 G>A maps to NM_022119.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:21045350 G>A maps to NM_017539.1 G1714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:21045350 G>A maps to NM_017539.1 G1714G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:31427864 C>T maps to ENST00000444228 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr16:31427864 C>T maps to ENST00000444228 N815N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr17:20924446 G>T maps to ENST00000455117 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr17:20924446 G>T maps to ENST00000455117 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr17:51901069 C>T maps to NM_032559.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr17:51901069 C>T maps to NM_032559.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:22363819 A>T maps to NM_001001411.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:22363819 A>T maps to NM_001001411.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:38983253 G>A maps to NM_000540.2 R2084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:38983253 G>A maps to NM_000540.2 R2084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:44589942 G>A maps to NM_001037813.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:44589942 G>A maps to NM_001037813.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:58084493 G>A maps to NM_017879.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr19:58084493 G>A maps to NM_017879.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr2:105473302 C>G maps to NM_006236.1 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr2:105473302 C>G maps to NM_006236.1 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr2:112786346 G>A maps to NM_006343.2 W969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr2:112786346 G>A maps to NM_006343.2 W969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr2:136627931 C>G did not map to a codon.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr2:136627931 C>G did not map to a codon.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr21:45786764 G>A maps to ENST00000397932 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr21:45786764 G>A maps to ENST00000397932 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:1019041 C>T maps to NM_021923.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:1019041 C>T maps to NM_021923.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:47945298 T>A maps to NM_001142564.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:47945298 T>A maps to NM_001142564.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:70160415 G>T maps to NM_053039.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:70160415 G>T maps to NM_053039.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:76836137 G>A maps to NM_014435.3 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:76836137 G>A maps to NM_014435.3 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:110437769 C>A maps to NM_006323.2 C700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr4:110437769 C>A maps to NM_006323.2 C700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr5:89821100 T>C maps to NM_198273.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr5:89821100 T>C maps to NM_198273.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr6:13470476 C>T maps to NM_033069.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr6:13470476 C>T maps to NM_033069.2 P12P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-32-1977-01A-01D-1353-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-32-1977-01A-01D-1353-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr7:74004216 C>T maps to NM_016328.2 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr7:74004216 C>T maps to NM_016328.2 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr7:134346604 A>T maps to NM_001724.4 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr7:134346604 A>T maps to NM_001724.4 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr8:26510764 G>A maps to NM_001197293.1 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr8:26510764 G>A maps to NM_001197293.1 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr9:136338316 G>A maps to NM_017585.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chr9:136338316 G>A maps to NM_017585.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chrX:37955450 C>T maps to NM_001163334.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1977-01A-01D-1353-08 chrX:37955450 C>T maps to NM_001163334.1 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr1:29069012 G>A maps to NM_016258.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr1:29069012 G>A maps to NM_016258.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr1:200842842 G>A maps to NM_005298.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr1:200842842 G>A maps to NM_005298.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr10:101716662 G>A maps to ENST00000342239 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr10:101716662 G>A maps to ENST00000342239 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr11:1956148 C>T maps to ENST00000397301 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr11:1956148 C>T maps to ENST00000397301 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr11:118085598 A>T did not map to a codon.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr11:118085598 A>T did not map to a codon.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr14:38724726 G>A maps to NM_175060.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr14:38724726 G>A maps to NM_175060.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr14:50626272 T>C maps to NM_006939.2 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr14:50626272 T>C maps to NM_006939.2 V576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr14:104639701 C>T maps to NM_015656.1 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr14:104639701 C>T maps to NM_015656.1 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr17:10406198 C>A maps to NM_005963.3 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr17:10406198 C>A maps to NM_005963.3 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr17:56247205 C>T maps to NM_001004707.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr17:56247205 C>T maps to NM_001004707.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:22363726 G>A maps to NM_001001411.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:22363726 G>A maps to NM_001001411.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:35719013 G>A maps to NM_152481.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:35719013 G>A maps to NM_152481.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:39051892 C>T maps to NM_000540.2 N4141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:39051892 C>T maps to NM_000540.2 N4141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:41512822 C>T maps to NM_000767.4 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:41512822 C>T maps to NM_000767.4 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:58579129 C>T maps to NM_007134.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr19:58579129 C>T maps to NM_007134.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr20:944737 G>A maps to NM_001029871.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr20:944737 G>A maps to NM_001029871.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr21:43161156 G>A maps to ENST00000352483 D780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr21:43161156 G>A maps to ENST00000352483 D780D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr3:178952151 A>G maps to NM_006218.2 *1069W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr3:178952151 A>G maps to NM_006218.2 *1069W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:48536559 A>C did not map to a codon.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:48536559 A>C did not map to a codon.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:70160486 G>A maps to NM_053039.1 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:70160486 G>A maps to NM_053039.1 W517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:73959896 T>C maps to NM_032217.3 G1742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:73959896 T>C maps to NM_032217.3 G1742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:164394679 G>A maps to NM_032136.4 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr4:164394679 G>A maps to NM_032136.4 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr5:2749814 G>A maps to NM_033267.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr5:2749814 G>A maps to NM_033267.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr5:45303808 G>A maps to NM_021072.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr5:45303808 G>A maps to NM_021072.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr5:131544872 C>T maps to NM_001142599.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr5:131544872 C>T maps to NM_001142599.1 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:12683929 C>T maps to NM_001112706.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:12683929 C>T maps to NM_001112706.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:50467928 G>A maps to NM_006060.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:50467928 G>A maps to NM_006060.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:142749460 C>T maps to NM_001001667.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:142749460 C>T maps to NM_001001667.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:147259236 C>T maps to NM_014141.5 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr7:147259236 C>T maps to NM_014141.5 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr9:130272451 G>A maps to NM_022833.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr9:130272451 G>A maps to NM_022833.2 N378N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chrX:70469492 G>T maps to ENST00000373988 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chrX:70469492 G>T maps to ENST00000373988 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chrX:125685358 G>A maps to NM_178470.4 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chrX:125685358 G>A maps to NM_178470.4 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr11:63273793 C>T did not map to a codon.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr11:63273793 C>T did not map to a codon.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr17:29663348 A>G did not map to a codon.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr17:29663348 A>G did not map to a codon.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr4:57777085 A>G maps to NM_005612.4 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr4:57777085 A>G maps to NM_005612.4 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr4:88415063 T>C maps to NM_004684.4 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr4:88415063 T>C maps to NM_004684.4 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr9:99581329 G>C maps to NM_001001662.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1980-01A-01D-1696-08 chr9:99581329 G>C maps to NM_001001662.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr1:39750771 C>T maps to ENST00000361689 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr1:39750771 C>T maps to ENST00000361689 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr1:235993675 G>A maps to NM_000081.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr1:235993675 G>A maps to NM_000081.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr10:24874105 G>A maps to NM_020824.3 S1704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr10:24874105 G>A maps to NM_020824.3 S1704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr10:38404216 G>T maps to NM_003421.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr10:38404216 G>T maps to NM_003421.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr12:40689280 G>A maps to NM_198578.3 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr12:40689280 G>A maps to NM_198578.3 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr12:85460675 G>T maps to NM_001079910.1 G899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr12:85460675 G>T maps to NM_001079910.1 G899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr14:23869929 G>A maps to NM_002471.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr14:23869929 G>A maps to NM_002471.3 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr14:95569922 C>T maps to NM_177438.2 V1270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr14:95569922 C>T maps to NM_177438.2 V1270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr16:56660825 G>A maps to NM_175617.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr16:56660825 G>A maps to NM_175617.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr16:68855964 C>T maps to NM_004360.3 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr16:68855964 C>T maps to NM_004360.3 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr17:56772379 A>G maps to NM_058216.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr17:56772379 A>G maps to NM_058216.1 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:8668747 G>A maps to NM_030957.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:8668747 G>A maps to NM_030957.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:9058870 G>T maps to NM_024690.2 T9525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:9058870 G>T maps to NM_024690.2 T9525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:51462467 G>A maps to NM_001012964.1 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:51462467 G>A maps to NM_001012964.1 N229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:56423178 G>A maps to NM_176810.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr19:56423178 G>A maps to NM_176810.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr2:1544410 C>T maps to NM_000547.5 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr2:1544410 C>T maps to NM_000547.5 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr2:21256279 C>A maps to NM_000384.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr2:21256279 C>A maps to NM_000384.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr2:196681638 C>T maps to NM_018897.2 S3158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr2:196681638 C>T maps to NM_018897.2 S3158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr3:53856598 G>A maps to NM_018397.4 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr3:53856598 G>A maps to NM_018397.4 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr5:150672977 G>A maps to NM_001145017.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr5:150672977 G>A maps to NM_001145017.1 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr6:136582519 T>C maps to NM_014739.2 K880K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr6:136582519 T>C maps to NM_014739.2 K880K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr6:152831379 G>A maps to NM_182961.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr6:152831379 G>A maps to NM_182961.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr7:103050960 G>A maps to ENST00000354356 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr7:103050960 G>A maps to ENST00000354356 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr7:142650950 G>A maps to NM_000420.2 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr7:142650950 G>A maps to NM_000420.2 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr7:143884177 G>A maps to NM_001003702.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr7:143884177 G>A maps to NM_001003702.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr8:24181417 G>A maps to NM_014265.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr8:24181417 G>A maps to NM_014265.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr9:112017852 C>T maps to NM_019114.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chr9:112017852 C>T maps to NM_019114.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:36103535 C>T maps to NM_173695.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:36103535 C>T maps to NM_173695.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:70627912 C>T maps to ENST00000449580 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:70627912 C>T maps to ENST00000449580 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:77378403 T>A maps to NM_000291.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:77378403 T>A maps to NM_000291.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:99662857 G>A maps to NM_001184880.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:99662857 G>A maps to NM_001184880.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:107084401 G>A maps to NM_012216.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1982-01A-01D-1494-08 chrX:107084401 G>A maps to NM_012216.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:3746423 G>A maps to NM_014704.3 N658N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:3746423 G>A maps to NM_014704.3 N658N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:67206952 A>T did not map to a codon.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:67206952 A>T did not map to a codon.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:154479755 G>C maps to NM_001098475.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:154479755 G>C maps to NM_001098475.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:160718191 C>A maps to NM_021181.3 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:160718191 C>A maps to NM_021181.3 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:228444457 G>A maps to NM_001098623.1 E1472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr1:228444457 G>A maps to NM_001098623.1 E1472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr11:65143940 G>A maps to NM_182556.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr11:65143940 G>A maps to NM_182556.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr12:7945666 C>T maps to NM_024865.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr12:7945666 C>T maps to NM_024865.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr15:38233921 C>T maps to NM_152453.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr15:38233921 C>T maps to NM_152453.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr15:43816805 T>C maps to ENST00000382031 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr15:43816805 T>C maps to ENST00000382031 A1283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr15:72432113 C>T maps to NM_145204.3 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr15:72432113 C>T maps to NM_145204.3 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr17:39535640 G>A maps to NM_021013.3 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr17:39535640 G>A maps to NM_021013.3 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr2:119732139 G>A maps to NM_006770.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr2:119732139 G>A maps to NM_006770.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr2:209036766 C>T maps to NM_001099334.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr2:209036766 C>T maps to NM_001099334.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr20:36668948 T>C maps to NM_021215.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr20:36668948 T>C maps to NM_021215.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr4:153897133 A>G maps to NM_033393.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr4:153897133 A>G maps to NM_033393.2 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr5:41149448 G>A maps to NM_001115131.1 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr5:41149448 G>A maps to NM_001115131.1 D839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr5:154311129 A>G maps to NM_015465.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1986-01A-01D-1494-08 chr5:154311129 A>G maps to NM_015465.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:152187645 T>C maps to NM_001009931.1 S2153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:152187645 T>C maps to NM_001009931.1 S2153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:179077668 C>T maps to NM_007314.3 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:179077668 C>T maps to NM_007314.3 P911P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:185144109 A>G maps to NM_001105518.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:185144109 A>G maps to NM_001105518.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:198703533 C>A maps to ENST00000271610 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr1:198703533 C>A maps to ENST00000271610 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr10:89717635 A>T maps to NM_000314.4 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr10:89717635 A>T maps to NM_000314.4 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr11:64337165 G>A maps to NM_018484.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr11:64337165 G>A maps to NM_018484.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr11:118521223 G>A maps to NM_015157.2 R1282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr11:118521223 G>A maps to NM_015157.2 R1282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr11:134104938 G>T maps to NM_052875.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr11:134104938 G>T maps to NM_052875.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr12:10539552 G>A maps to NM_007360.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr12:10539552 G>A maps to NM_007360.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr14:95932330 G>A maps to NM_152592.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr14:95932330 G>A maps to NM_152592.3 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr15:30664455 C>T maps to NM_139320.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr15:30664455 C>T maps to NM_139320.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr15:53998127 A>G maps to NM_182758.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr15:53998127 A>G maps to NM_182758.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr15:101972224 G>A maps to NM_002570.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr15:101972224 G>A maps to NM_002570.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr16:67183809 C>A maps to NM_033309.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr16:67183809 C>A maps to NM_033309.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr19:49510607 C>T maps to NM_006666.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr19:49510607 C>T maps to NM_006666.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr19:49519327 G>T maps to NM_000894.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr19:49519327 G>T maps to NM_000894.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr19:50270422 G>A maps to NM_014203.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr19:50270422 G>A maps to NM_014203.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr2:43458374 G>A maps to ENST00000330266 S1859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr2:43458374 G>A maps to ENST00000330266 S1859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr2:170850839 G>A maps to ENST00000442603 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr2:170850839 G>A maps to ENST00000442603 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr2:208841552 A>G maps to NM_001080475.2 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr2:208841552 A>G maps to NM_001080475.2 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr3:42905967 C>T did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr3:42905967 C>T did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr4:25127314 C>T did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr4:25127314 C>T did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr5:32739136 G>A did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr5:32739136 G>A did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr5:150133219 C>A did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr5:150133219 C>A did not map to a codon.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr6:136599813 G>A maps to NM_014739.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr6:136599813 G>A maps to NM_014739.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr8:6794409 G>A maps to NM_001925.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr8:6794409 G>A maps to NM_001925.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr8:23538760 C>T maps to NM_006167.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr8:23538760 C>T maps to NM_006167.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr8:124442260 A>G maps to NM_018024.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr8:124442260 A>G maps to NM_018024.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr9:92220749 C>T maps to NM_006705.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr9:92220749 C>T maps to NM_006705.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr9:98728903 G>T maps to NM_001010895.2 G681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1991-01A-01D-1353-08 chr9:98728903 G>T maps to NM_001010895.2 G681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr1:3684009 G>A did not map to a codon.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr1:3684009 G>A did not map to a codon.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr1:74507036 A>G maps to NM_001105659.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr1:74507036 A>G maps to NM_001105659.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr1:228404989 G>T did not map to a codon.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr1:228404989 G>T did not map to a codon.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr10:64950736 G>A maps to NM_032776.1 L2070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr10:64950736 G>A maps to NM_032776.1 L2070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:3688948 C>T maps to NM_020402.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:3688948 C>T maps to NM_020402.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:47726093 C>G did not map to a codon.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:47726093 C>G did not map to a codon.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:62378667 C>A maps to ENST00000278845 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:62378667 C>A maps to ENST00000278845 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:119206266 T>A maps to NM_032015.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr11:119206266 T>A maps to NM_032015.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr12:111099055 G>A maps to NM_001040107.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr12:111099055 G>A maps to NM_001040107.1 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr13:48955549 C>T maps to NM_000321.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr13:48955549 C>T maps to NM_000321.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr15:101933602 G>A maps to NM_002570.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr15:101933602 G>A maps to NM_002570.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr16:31422195 G>A maps to ENST00000444228 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr16:31422195 G>A maps to ENST00000444228 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr17:26818572 C>T maps to NM_001145975.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr17:26818572 C>T maps to NM_001145975.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:10434233 G>A maps to NM_133452.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:10434233 G>A maps to NM_133452.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:40901147 T>C maps to NM_181882.2 E1037E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:40901147 T>C maps to NM_181882.2 E1037E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:41248415 G>A maps to NM_198476.3 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:41248415 G>A maps to NM_198476.3 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:53793036 G>A maps to NM_033341.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr19:53793036 G>A maps to NM_033341.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr2:231106158 C>T maps to NM_007237.4 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr2:231106158 C>T maps to NM_007237.4 N149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr20:50140359 C>T maps to NM_012340.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr20:50140359 C>T maps to NM_012340.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr3:15115966 C>A maps to NM_022340.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr3:15115966 C>A maps to NM_022340.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr3:52778290 G>A maps to NM_003157.4 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr3:52778290 G>A maps to NM_003157.4 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr4:104117133 T>C maps to NM_001813.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr4:104117133 T>C maps to NM_001813.2 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr4:185018422 C>G maps to NM_153343.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr4:185018422 C>G maps to NM_153343.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr5:23527860 C>T maps to NM_020227.2 Y888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr5:23527860 C>T maps to NM_020227.2 Y888Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr5:179318429 G>A maps to NM_198868.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr5:179318429 G>A maps to NM_198868.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr6:31508153 G>C maps to ENST00000417556 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr6:31508153 G>C maps to ENST00000417556 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr6:31933759 C>A maps to NM_006929.4 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr6:31933759 C>A maps to NM_006929.4 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr7:30795055 G>A maps to NM_006774.4 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr7:30795055 G>A maps to NM_006774.4 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr8:30694496 C>T maps to NM_031271.3 A2718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr8:30694496 C>T maps to NM_031271.3 A2718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr9:18777019 T>C maps to NM_001040272.4 Y931Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr9:18777019 T>C maps to NM_001040272.4 Y931Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr9:33467805 C>T maps to NM_022917.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2491-01A-01D-1353-08 chr9:33467805 C>T maps to NM_022917.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr1:53925198 G>T maps to NM_033067.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr1:53925198 G>T maps to NM_033067.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr1:158450131 T>C maps to NM_001004472.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr1:158450131 T>C maps to NM_001004472.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr1:167667015 C>T maps to NM_052862.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr1:167667015 C>T maps to NM_052862.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr11:35226084 G>T maps to NM_000610.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr11:35226084 G>T maps to NM_000610.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr11:48134461 C>T maps to NM_002843.3 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr11:48134461 C>T maps to NM_002843.3 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr12:104147040 G>A maps to NM_017564.9 Q2208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr12:104147040 G>A maps to NM_017564.9 Q2208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr15:65495752 G>A maps to NM_003613.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr15:65495752 G>A maps to NM_003613.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr16:4033330 C>T maps to NM_001116.3 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr16:4033330 C>T maps to NM_001116.3 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr16:53500989 G>T maps to NM_005611.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr16:53500989 G>T maps to NM_005611.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr17:7163800 G>A maps to NM_001185022.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr17:7163800 G>A maps to NM_001185022.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr17:14139673 G>A maps to NM_001007530.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr17:14139673 G>A maps to NM_001007530.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr17:29508437 A>G did not map to a codon.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr17:29508437 A>G did not map to a codon.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr18:61585320 G>A maps to NM_005024.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr18:61585320 G>A maps to NM_005024.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr19:47979803 G>A maps to NM_007059.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr19:47979803 G>A maps to NM_007059.2 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr2:48915480 C>A maps to NM_000233.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr2:48915480 C>A maps to NM_000233.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr21:31874369 G>A maps to NM_181611.1 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr21:31874369 G>A maps to NM_181611.1 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr3:1339582 G>T maps to NM_014461.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr3:1339582 G>T maps to NM_014461.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr3:40231527 G>A maps to NM_015460.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr3:40231527 G>A maps to NM_015460.2 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr3:195012472 C>T maps to NM_012287.5 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr3:195012472 C>T maps to NM_012287.5 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr7:2255874 C>T maps to NM_003550.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr7:2255874 C>T maps to NM_003550.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr7:142575506 C>T maps to NM_018646.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr7:142575506 C>T maps to NM_018646.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr8:26492399 C>A maps to NM_001197293.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chr8:26492399 C>A maps to NM_001197293.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chrX:64721738 G>A maps to NM_001010888.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chrX:64721738 G>A maps to NM_001010888.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chrX:69263787 A>G maps to NM_001002254.1 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chrX:69263787 A>G maps to NM_001002254.1 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chrX:129492633 A>G maps to ENST00000339231 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2494-01A-01D-1353-08 chrX:129492633 A>G maps to ENST00000339231 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:16377395 G>A maps to NM_000085.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:16377395 G>A maps to NM_000085.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:90179097 T>C maps to NM_032270.4 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:90179097 T>C maps to NM_032270.4 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:167353106 G>A maps to NM_002697.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:167353106 G>A maps to NM_002697.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:248525115 C>A maps to NM_001004696.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr1:248525115 C>A maps to NM_001004696.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr10:63816873 A>C did not map to a codon.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr10:63816873 A>C did not map to a codon.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr10:112655707 T>C maps to NM_014456.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr10:112655707 T>C maps to NM_014456.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr11:63487656 C>T maps to ENST00000377819 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr11:63487656 C>T maps to ENST00000377819 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr11:65088798 G>T maps to NM_006779.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr11:65088798 G>T maps to NM_006779.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr12:118198973 C>T maps to ENST00000339824 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr12:118198973 C>T maps to ENST00000339824 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr14:24901648 G>C maps to NM_015299.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr14:24901648 G>C maps to NM_015299.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr15:24924481 G>A maps to NM_018958.2 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr15:24924481 G>A maps to NM_018958.2 P1156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr17:8219093 C>T maps to NM_173728.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr17:8219093 C>T maps to NM_173728.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:14105941 A>G maps to NM_145287.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:14105941 A>G maps to NM_145287.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:33740956 C>G maps to ENST00000442325 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:33740956 C>G maps to ENST00000442325 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:77246686 C>T maps to NM_172387.1 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:77246686 C>T maps to NM_172387.1 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:77679329 C>T maps to NM_025078.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr18:77679329 C>T maps to NM_025078.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:38990562 G>A maps to NM_000540.2 P2410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:38990562 G>A maps to NM_000540.2 P2410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:49253749 G>A maps to NM_000148.3 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:49253749 G>A maps to NM_000148.3 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:52918767 C>G maps to NM_032423.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:52918767 C>G maps to NM_032423.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:58723891 C>T maps to NM_133502.1 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr19:58723891 C>T maps to NM_133502.1 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr2:197521486 C>T maps to NM_001080539.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr2:197521486 C>T maps to NM_001080539.1 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr21:31971187 G>A maps to NM_181604.1 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr21:31971187 G>A maps to NM_181604.1 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr22:29147227 G>A did not map to a codon.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr22:29147227 G>A did not map to a codon.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr3:38355343 C>G maps to NM_004803.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr3:38355343 C>G maps to NM_004803.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr3:45153845 A>G maps to NM_022842.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr3:45153845 A>G maps to NM_022842.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr5:131296259 G>A maps to NM_001009185.1 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr5:131296259 G>A maps to NM_001009185.1 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:31742302 C>A maps to NM_025258.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:31742302 C>A maps to NM_025258.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:32797851 C>T maps to ENST00000452392 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:32797851 C>T maps to ENST00000452392 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:49700906 C>T did not map to a codon.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:49700906 C>T did not map to a codon.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:86203691 T>C maps to NM_002526.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr6:86203691 T>C maps to NM_002526.2 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr7:107703419 G>A maps to NM_007356.2 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr7:107703419 G>A maps to NM_007356.2 S1027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr7:150645538 C>T maps to NM_000238.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr7:150645538 C>T maps to NM_000238.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr8:113420583 T>C maps to NM_198123.1 G1856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chr8:113420583 T>C maps to NM_198123.1 G1856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chrX:2933416 A>G maps to NM_001011719.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chrX:2933416 A>G maps to NM_001011719.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chrX:53571566 G>A maps to ENST00000276009 D3737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chrX:53571566 G>A maps to ENST00000276009 D3737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chrX:153694759 G>A maps to NM_017514.3 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2495-01A-01D-1353-08 chrX:153694759 G>A maps to NM_017514.3 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:51001130 T>C did not map to a codon.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:51001130 T>C did not map to a codon.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:116666895 C>T maps to NM_152367.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:116666895 C>T maps to NM_152367.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:176993824 C>A maps to ENST00000281881 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:176993824 C>A maps to ENST00000281881 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:214209143 C>G maps to NM_002763.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr1:214209143 C>G maps to NM_002763.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr10:8006393 A>G maps to NM_031923.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr10:8006393 A>G maps to NM_031923.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr10:88419054 C>T maps to NM_001030015.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr10:88419054 C>T maps to NM_001030015.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr11:113853895 C>T maps to NM_213621.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr11:113853895 C>T maps to NM_213621.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr13:70314590 T>C maps to NM_020866.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr13:70314590 T>C maps to NM_020866.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr19:10678075 G>A maps to NM_079421.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr19:10678075 G>A maps to NM_079421.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr19:48342914 G>A maps to NM_000554.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr19:48342914 G>A maps to NM_000554.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr2:21233705 G>A maps to NM_000384.2 R2012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr2:21233705 G>A maps to NM_000384.2 R2012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr22:43831124 C>T maps to NM_001044370.1 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr22:43831124 C>T maps to NM_001044370.1 N132N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr4:13605550 T>C maps to NM_148894.2 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr4:13605550 T>C maps to NM_148894.2 R991R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr5:145428730 C>T maps to NM_152550.3 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr5:145428730 C>T maps to NM_152550.3 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr6:27861563 C>T maps to NM_003527.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr6:27861563 C>T maps to NM_003527.4 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr6:43325084 G>A maps to NM_014345.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr6:43325084 G>A maps to NM_014345.2 R323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr7:139746775 C>T maps to NM_022750.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr7:139746775 C>T maps to NM_022750.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr8:56270318 A>G maps to NM_052898.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr8:56270318 A>G maps to NM_052898.1 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr8:145624368 G>A maps to NM_013291.2 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr8:145624368 G>A maps to NM_013291.2 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr9:133342179 C>T maps to NM_000050.4 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chr9:133342179 C>T maps to NM_000050.4 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chrX:136649605 G>A maps to NM_003413.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2615-01A-01D-1495-08 chrX:136649605 G>A maps to NM_003413.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr1:152278814 G>A maps to NM_002016.1 D2849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr1:152278814 G>A maps to NM_002016.1 D2849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr11:48285738 G>A maps to NM_001004726.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr11:48285738 G>A maps to NM_001004726.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr12:72771777 C>T maps to NM_013381.2 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr12:72771777 C>T maps to NM_013381.2 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr13:113485795 C>T maps to NM_032189.3 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr13:113485795 C>T maps to NM_032189.3 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr14:104481127 C>T maps to NM_153046.2 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr14:104481127 C>T maps to NM_153046.2 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr17:39597029 G>A maps to NM_006771.3 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr17:39597029 G>A maps to NM_006771.3 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr18:29784270 G>A maps to NM_005925.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr18:29784270 G>A maps to NM_005925.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr18:60017105 G>A maps to NM_003839.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr18:60017105 G>A maps to NM_003839.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr19:17452116 G>A maps to NM_133644.3 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr19:17452116 G>A maps to NM_133644.3 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr19:18468320 C>T maps to NM_017712.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr19:18468320 C>T maps to NM_017712.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr19:46914657 C>T maps to NM_032040.3 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr19:46914657 C>T maps to NM_032040.3 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr2:167273363 G>A maps to NM_002976.2 D1089D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr2:167273363 G>A maps to NM_002976.2 D1089D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr2:191862989 G>A maps to NM_007315.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr2:191862989 G>A maps to NM_007315.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr20:34526876 G>A maps to NM_016436.4 Q853Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr20:34526876 G>A maps to NM_016436.4 Q853Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr21:28217206 G>T maps to NM_006988.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr21:28217206 G>T maps to NM_006988.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr3:50324237 C>T maps to NM_153215.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr3:50324237 C>T maps to NM_153215.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr3:108279494 C>T did not map to a codon.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr3:108279494 C>T did not map to a codon.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr3:156763370 C>T maps to NM_001004316.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr3:156763370 C>T maps to NM_001004316.2 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr4:8472817 A>G maps to NM_152544.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr4:8472817 A>G maps to NM_152544.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr4:8588807 C>T maps to NM_080819.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr4:8588807 C>T maps to NM_080819.2 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:1244740 G>A maps to NM_182632.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:1244740 G>A maps to NM_182632.2 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:55083675 G>A maps to NM_024415.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:55083675 G>A maps to NM_024415.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:147796555 G>C did not map to a codon.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:147796555 G>C did not map to a codon.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:161324317 C>T maps to NM_001127648.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr5:161324317 C>T maps to NM_001127648.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr6:136682256 C>T maps to NM_001198609.1 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr6:136682256 C>T maps to NM_001198609.1 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr7:4820907 C>T maps to ENST00000450194 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr7:4820907 C>T maps to ENST00000450194 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr7:31682399 G>A maps to NM_194300.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr7:31682399 G>A maps to NM_194300.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr8:25265579 C>T maps to NM_024940.6 S1725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr8:25265579 C>T maps to NM_024940.6 S1725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr8:27308399 G>A maps to NM_004103.3 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr8:27308399 G>A maps to NM_004103.3 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr8:75227466 C>T maps to NM_020647.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr8:75227466 C>T maps to NM_020647.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr9:134016057 C>T maps to ENST00000451030 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chr9:134016057 C>T maps to ENST00000451030 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chrX:32486812 A>G maps to ENST00000357033 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2632-01A-01D-1495-08 chrX:32486812 A>G maps to ENST00000357033 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr10:104158520 G>T maps to NM_001077494.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr10:104158520 G>T maps to NM_001077494.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr11:5020754 T>C maps to NM_001004755.1 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr11:5020754 T>C maps to NM_001004755.1 C181C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr11:59225155 G>A maps to NM_001004708.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr11:59225155 G>A maps to NM_001004708.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr11:130130850 A>T maps to ENST00000397753 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr11:130130850 A>T maps to ENST00000397753 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr12:104461816 T>C maps to NM_013320.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr12:104461816 T>C maps to NM_013320.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr13:49039229 C>T maps to NM_000321.2 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr13:49039229 C>T maps to NM_000321.2 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr14:95033523 T>A maps to NM_006215.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr14:95033523 T>A maps to NM_006215.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr15:43817783 C>T maps to ENST00000382031 D1609D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr15:43817783 C>T maps to ENST00000382031 D1609D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr19:4207776 G>A did not map to a codon.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr19:4207776 G>A did not map to a codon.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr19:13355995 C>T maps to NM_023035.2 G1654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr19:13355995 C>T maps to NM_023035.2 G1654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr19:36051415 G>A maps to NM_000704.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr19:36051415 G>A maps to NM_000704.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr2:192546716 G>A maps to NM_001031716.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr2:192546716 G>A maps to NM_001031716.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr20:1424443 G>A maps to ENST00000476071 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr20:1424443 G>A maps to ENST00000476071 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr5:67591120 C>T maps to ENST00000396611 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr5:67591120 C>T maps to ENST00000396611 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr5:121187840 C>T maps to NM_177478.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr5:121187840 C>T maps to NM_177478.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr6:163235308 G>A maps to NM_152410.2 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr6:163235308 G>A maps to NM_152410.2 W96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr7:66240357 T>C maps to ENST00000451741 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chr7:66240357 T>C maps to ENST00000451741 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chrX:115573955 G>T maps to NM_007231.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2634-01A-01D-1495-08 chrX:115573955 G>T maps to NM_007231.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:155449240 G>C maps to ENST00000368346 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:155449240 G>C maps to ENST00000368346 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:216595555 C>T maps to ENST00000366943 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:216595555 C>T maps to ENST00000366943 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:228564890 G>A maps to NM_001098623.1 P7726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:228564890 G>A maps to NM_001098623.1 P7726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:238048806 C>G maps to NM_021186.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr1:238048806 C>G maps to NM_021186.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr11:58978682 C>T maps to NM_001039396.1 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr11:58978682 C>T maps to NM_001039396.1 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr11:71260047 T>C maps to NM_005553.3 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr11:71260047 T>C maps to NM_005553.3 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr11:121037458 C>T maps to NM_005422.2 N1852N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr11:121037458 C>T maps to NM_005422.2 N1852N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr13:77459428 G>A maps to NM_138444.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr13:77459428 G>A maps to NM_138444.3 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr14:63447808 C>T maps to NM_139318.3 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr14:63447808 C>T maps to NM_139318.3 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr14:94933657 G>A maps to NM_175739.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr14:94933657 G>A maps to NM_175739.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr17:440382 G>A maps to NM_001128159.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr17:440382 G>A maps to NM_001128159.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr17:38062399 G>A maps to NM_001165958.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr17:38062399 G>A maps to NM_001165958.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr17:66981087 C>T maps to NM_080283.3 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr17:66981087 C>T maps to NM_080283.3 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr19:7965734 G>T maps to NM_025061.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr19:7965734 G>T maps to NM_025061.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr19:9072142 T>A maps to NM_024690.2 S5101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr19:9072142 T>A maps to NM_024690.2 S5101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr2:25674484 G>A maps to NM_021907.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr2:25674484 G>A maps to NM_021907.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr22:41790268 C>A maps to ENST00000417325 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr22:41790268 C>A maps to ENST00000417325 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr3:21792471 G>A did not map to a codon.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr3:21792471 G>A did not map to a codon.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr3:67570992 G>C maps to NM_003848.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr3:67570992 G>C maps to NM_003848.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr3:141497200 C>T maps to NM_139209.2 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr3:141497200 C>T maps to NM_139209.2 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr4:78804479 C>T maps to NM_020236.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr4:78804479 C>T maps to NM_020236.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr4:96090459 G>A maps to NM_003728.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr4:96090459 G>A maps to NM_003728.3 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr4:164054387 A>G maps to NM_138386.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr4:164054387 A>G maps to NM_138386.2 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr6:124979423 T>A maps to NM_001040214.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr6:124979423 T>A maps to NM_001040214.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr6:161134137 C>T maps to NM_000301.3 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr6:161134137 C>T maps to NM_000301.3 C176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr7:88965892 A>G maps to NM_181646.2 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr7:88965892 A>G maps to NM_181646.2 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr7:100680858 G>A maps to NM_001040105.1 T2054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr7:100680858 G>A maps to NM_001040105.1 T2054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr9:140638535 C>A maps to NM_024757.4 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chr9:140638535 C>A maps to NM_024757.4 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chrX:69283225 C>G maps to NM_207320.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-2638-01A-01D-1495-08 chrX:69283225 C>G maps to NM_207320.1 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr1:12052618 C>G maps to NM_014874.3 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr1:12052618 C>G maps to NM_014874.3 Y61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr1:101339635 A>G maps to NM_001439.2 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr1:101339635 A>G maps to NM_001439.2 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr1:185878605 G>A maps to NM_031935.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr1:185878605 G>A maps to NM_031935.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr11:64602004 C>T maps to NM_017525.2 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr11:64602004 C>T maps to NM_017525.2 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr14:77292857 C>G maps to NM_194287.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr14:77292857 C>G maps to NM_194287.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr16:23360057 C>A maps to ENST00000307331 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr16:23360057 C>A maps to ENST00000307331 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr17:56083326 A>G maps to NM_006924.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr17:56083326 A>G maps to NM_006924.4 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr5:178040531 C>T maps to NM_020666.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr5:178040531 C>T maps to NM_020666.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr6:17831466 C>A did not map to a codon.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr6:17831466 C>A did not map to a codon.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr6:151336801 C>T maps to NM_015440.3 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr6:151336801 C>T maps to NM_015440.3 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr7:128415065 G>T maps to NM_001708.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr7:128415065 G>T maps to NM_001708.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr7:150915907 G>A maps to NM_005692.3 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr7:150915907 G>A maps to NM_005692.3 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr8:85774531 T>C maps to NM_001100391.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr8:85774531 T>C maps to NM_001100391.1 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr8:144991997 G>C maps to NM_201380.2 G4134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr8:144991997 G>C maps to NM_201380.2 G4134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr9:35386178 C>T maps to ENST00000396787 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chr9:35386178 C>T maps to ENST00000396787 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chrX:76938028 G>A maps to NM_000489.3 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4208-01A-01D-1353-08 chrX:76938028 G>A maps to NM_000489.3 R907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr1:151755432 C>T maps to NM_001083965.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr1:151755432 C>T maps to NM_001083965.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr10:101960489 A>G maps to NM_001278.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr10:101960489 A>G maps to NM_001278.3 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr12:55846833 C>T maps to NM_054105.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr12:55846833 C>T maps to NM_054105.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr12:99007866 T>C maps to NM_201612.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr12:99007866 T>C maps to NM_201612.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr14:23312493 C>T maps to NM_004995.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr14:23312493 C>T maps to NM_004995.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr17:40847560 G>A maps to NM_003632.2 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr17:40847560 G>A maps to NM_003632.2 P1005P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr17:80842048 C>T maps to NM_005993.4 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr17:80842048 C>T maps to NM_005993.4 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr19:22846756 G>T maps to NM_020855.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr19:22846756 G>T maps to NM_020855.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr2:149793796 G>A did not map to a codon.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr2:149793796 G>A did not map to a codon.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr3:120871385 A>G maps to NM_014980.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr3:120871385 A>G maps to NM_014980.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr6:70589453 G>T did not map to a codon.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr6:70589453 G>T did not map to a codon.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr7:73771698 G>A maps to NM_003388.4 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4209-01A-01D-1353-08 chr7:73771698 G>A maps to NM_003388.4 E369E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr1:24409116 G>A maps to ENST00000330966 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr1:24409116 G>A maps to ENST00000330966 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr1:68948413 T>C maps to NM_001114120.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr1:68948413 T>C maps to NM_001114120.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr1:114225543 G>A maps to NM_001142782.1 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr1:114225543 G>A maps to NM_001142782.1 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr10:15701006 C>T maps to NM_003638.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr10:15701006 C>T maps to NM_003638.1 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr10:27702996 C>T maps to NM_001034842.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr10:27702996 C>T maps to NM_001034842.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr11:554077 T>C maps to NM_198075.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr11:554077 T>C maps to NM_198075.3 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr11:64024114 C>T maps to NM_000932.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr11:64024114 C>T maps to NM_000932.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:108010912 C>T maps to NM_001018072.1 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:108010912 C>T maps to NM_001018072.1 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:117993075 T>C maps to ENST00000339824 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:117993075 T>C maps to ENST00000339824 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:122702872 G>T maps to NM_019887.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:122702872 G>T maps to NM_019887.4 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:131593381 G>A maps to NM_198827.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr12:131593381 G>A maps to NM_198827.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr14:44975413 A>G maps to NM_032135.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr14:44975413 A>G maps to NM_032135.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:1270780 C>T maps to NM_021098.2 D2283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:1270780 C>T maps to NM_021098.2 D2283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:3339528 G>A maps to NM_005741.4 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:3339528 G>A maps to NM_005741.4 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:67914752 A>G maps to NM_014329.3 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:67914752 A>G maps to NM_014329.3 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:81942160 C>T maps to NM_002661.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr16:81942160 C>T maps to NM_002661.2 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr17:7943286 G>A maps to NM_001141.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr17:7943286 G>A maps to NM_001141.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr18:580605 G>A maps to NM_004066.1 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr18:580605 G>A maps to NM_004066.1 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:6531064 C>T maps to NM_003811.3 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:6531064 C>T maps to NM_003811.3 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:12779319 A>G did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:12779319 A>G did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:42133313 G>A maps to NM_001817.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:42133313 G>A maps to NM_001817.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:54823149 C>T maps to NM_021250.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:54823149 C>T maps to NM_021250.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:56422071 G>A maps to NM_176810.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr19:56422071 G>A maps to NM_176810.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr2:179485011 G>A maps to NM_133378.4 C12844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr2:179485011 G>A maps to NM_133378.4 C12844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr3:196735735 G>C maps to NM_005929.5 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr3:196735735 G>C maps to NM_005929.5 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr4:87671854 A>G maps to NM_080685.2 E961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr4:87671854 A>G maps to NM_080685.2 E961E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr5:140832 T>G did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr5:140832 T>G did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr5:40681331 G>A maps to NM_000958.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr5:40681331 G>A maps to NM_000958.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr5:140432383 C>T maps to NM_013340.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr5:140432383 C>T maps to NM_013340.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:30675375 C>A maps to NM_014641.2 G994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:30675375 C>A maps to NM_014641.2 G994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:56476385 A>G maps to ENST00000361203 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:56476385 A>G maps to ENST00000361203 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:151117038 G>T did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:151117038 G>T did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:152792794 C>T maps to NM_182961.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr6:152792794 C>T maps to NM_182961.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:5330387 C>T maps to NM_153247.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:5330387 C>T maps to NM_153247.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:92158935 T>C maps to NM_032120.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:92158935 T>C maps to NM_032120.2 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:92821586 G>A maps to ENST00000453812 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:92821586 G>A maps to ENST00000453812 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:117864827 C>T did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr7:117864827 C>T did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr8:65517237 C>A did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr8:65517237 C>A did not map to a codon.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr8:145806267 C>G maps to NM_025251.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4210-01A-01D-1353-08 chr8:145806267 C>G maps to NM_025251.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:12726354 G>A maps to NM_001013630.1 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:12726354 G>A maps to NM_001013630.1 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:31210477 G>A maps to NM_006762.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:31210477 G>A maps to NM_006762.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:215848823 C>T maps to ENST00000366943 S4143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:215848823 C>T maps to ENST00000366943 S4143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:224586246 G>A maps to NM_025160.6 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr1:224586246 G>A maps to NM_025160.6 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr10:23235137 A>G maps to NM_173081.3 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr10:23235137 A>G maps to NM_173081.3 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:83251228 C>G maps to NM_152588.1 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:83251228 C>G maps to NM_152588.1 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:83251307 C>G maps to NM_152588.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:83251307 C>G maps to NM_152588.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:83251313 C>G maps to NM_152588.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:83251313 C>G maps to NM_152588.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:114832608 C>T maps to NM_000192.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr12:114832608 C>T maps to NM_000192.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr14:80130233 C>T maps to NM_004796.4 N813N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr14:80130233 C>T maps to NM_004796.4 N813N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr15:45556869 G>A maps to NM_004212.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr15:45556869 G>A maps to NM_004212.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr16:50763749 C>T maps to NM_022162.1 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr16:50763749 C>T maps to NM_022162.1 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr16:88643656 G>A maps to ENST00000452588 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr16:88643656 G>A maps to ENST00000452588 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr17:27899698 C>T maps to NM_138349.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr17:27899698 C>T maps to NM_138349.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr17:40065322 T>G did not map to a codon.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr17:40065322 T>G did not map to a codon.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr18:7036078 C>T maps to NM_005559.2 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr18:7036078 C>T maps to NM_005559.2 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr19:44933458 A>G maps to NM_014518.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr19:44933458 A>G maps to NM_014518.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr2:29443571 C>T maps to NM_004304.3 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr2:29443571 C>T maps to NM_004304.3 P1215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr21:47355173 C>T maps to NM_020528.2 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr21:47355173 C>T maps to NM_020528.2 D288D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-32-4211-01A-01D-1353-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-32-4211-01A-01D-1353-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr3:140178465 C>T maps to NM_022131.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr3:140178465 C>T maps to NM_022131.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr4:1018885 G>A maps to NM_021923.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr4:1018885 G>A maps to NM_021923.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr4:111553637 T>A did not map to a codon.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr4:111553637 T>A did not map to a codon.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr5:125822669 G>T did not map to a codon.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr5:125822669 G>T did not map to a codon.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr5:156916127 C>T maps to ENST00000430702 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr5:156916127 C>T maps to ENST00000430702 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr6:43415636 C>T maps to NM_033450.2 D1279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr6:43415636 C>T maps to NM_033450.2 D1279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr7:37780660 G>A maps to NM_181791.1 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr7:37780660 G>A maps to NM_181791.1 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr7:143792751 C>T maps to NM_001004135.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr7:143792751 C>T maps to NM_001004135.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr8:59409722 C>T maps to NM_000780.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr8:59409722 C>T maps to NM_000780.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr8:144733274 G>A maps to NM_014789.3 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4211-01A-01D-1353-08 chr8:144733274 G>A maps to NM_014789.3 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr1:6171854 C>T maps to NM_015557.2 W1743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr1:6171854 C>T maps to NM_015557.2 W1743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr1:23660031 C>T maps to ENST00000414299 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr1:23660031 C>T maps to ENST00000414299 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr1:145439906 C>T maps to NM_006472.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr1:145439906 C>T maps to NM_006472.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr10:46999947 G>A maps to NM_014696.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr10:46999947 G>A maps to NM_014696.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr10:105145151 G>A maps to NM_006951.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr10:105145151 G>A maps to NM_006951.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr11:60785321 G>C maps to NM_006725.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr11:60785321 G>C maps to NM_006725.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr12:21201832 C>A maps to ENST00000381541 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr12:21201832 C>A maps to ENST00000381541 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr12:53709175 G>A maps to NM_015665.5 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr12:53709175 G>A maps to NM_015665.5 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr14:70990595 A>G maps to NM_003814.4 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr14:70990595 A>G maps to NM_003814.4 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr15:34080623 C>T maps to NM_001036.3 F3265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr15:34080623 C>T maps to NM_001036.3 F3265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr17:1936937 C>A maps to NM_001383.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr17:1936937 C>A maps to NM_001383.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr17:39594784 C>T maps to NM_006771.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr17:39594784 C>T maps to NM_006771.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr18:14533124 A>G maps to ENST00000444806 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr18:14533124 A>G maps to ENST00000444806 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr19:17330165 C>T maps to NM_018467.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr19:17330165 C>T maps to NM_018467.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr19:21131688 G>A maps to NM_003429.4 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr19:21131688 G>A maps to NM_003429.4 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr2:220046154 C>T maps to NM_024293.4 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr2:220046154 C>T maps to NM_024293.4 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr2:240002803 A>G maps to NM_006037.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr2:240002803 A>G maps to NM_006037.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr21:45503035 A>G maps to NM_003274.4 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr21:45503035 A>G maps to NM_003274.4 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr22:50967630 G>A maps to ENST00000395681 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr22:50967630 G>A maps to ENST00000395681 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr4:74464407 G>T maps to NM_201431.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr4:74464407 G>T maps to NM_201431.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr5:13883071 C>A maps to NM_001369.2 E1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr5:13883071 C>A maps to NM_001369.2 E1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr5:77473218 T>G maps to NM_003664.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr5:77473218 T>G maps to NM_003664.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr8:27362584 G>A maps to ENST00000458037 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr8:27362584 G>A maps to ENST00000458037 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr8:87229697 C>T did not map to a codon.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr8:87229697 C>T did not map to a codon.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr9:35396551 C>A maps to ENST00000396787 Y1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chr9:35396551 C>A maps to ENST00000396787 Y1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chrX:40562699 T>C maps to NM_004229.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chrX:40562699 T>C maps to NM_004229.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chrX:64722248 C>T maps to NM_001010888.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chrX:64722248 C>T maps to NM_001010888.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chrX:107404861 A>G maps to NM_033641.2 P1440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4213-01A-01D-1353-08 chrX:107404861 A>G maps to NM_033641.2 P1440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr11:46894745 G>A maps to ENST00000256991 I1541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr11:46894745 G>A maps to ENST00000256991 I1541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr12:60169206 T>G maps to NM_004731.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr12:60169206 T>G maps to NM_004731.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr16:20376784 G>A maps to NM_174924.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr16:20376784 G>A maps to NM_174924.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr16:88705561 G>A maps to NM_013278.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr16:88705561 G>A maps to NM_013278.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr17:38340588 C>T maps to ENST00000456989 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr17:38340588 C>T maps to ENST00000456989 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr18:6982556 C>T maps to NM_005559.2 A1943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr18:6982556 C>T maps to NM_005559.2 A1943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr19:47844106 G>A maps to NM_018485.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr19:47844106 G>A maps to NM_018485.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr22:46931594 G>A maps to NM_014246.1 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr22:46931594 G>A maps to NM_014246.1 N491N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr3:15778599 G>A maps to NM_015199.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr3:15778599 G>A maps to NM_015199.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr4:16204131 A>G maps to NM_153365.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr4:16204131 A>G maps to NM_153365.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr7:20767946 G>A maps to NM_001163941.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr7:20767946 G>A maps to NM_001163941.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr9:426981 G>T did not map to a codon.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr9:426981 G>T did not map to a codon.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr1:91182731 G>A maps to NM_020063.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr1:91182731 G>A maps to NM_020063.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr1:152325928 G>A maps to NM_001014342.2 Q1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr1:152325928 G>A maps to NM_001014342.2 Q1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr1:179084043 G>A maps to NM_007314.3 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr1:179084043 G>A maps to NM_007314.3 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr11:64335160 C>T maps to NM_018484.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr11:64335160 C>T maps to NM_018484.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:8212172 C>T maps to NM_004054.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:8212172 C>T maps to NM_004054.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:56436345 C>T maps to NM_001029.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:56436345 C>T maps to NM_001029.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:71523125 T>C maps to NM_004616.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:71523125 T>C maps to NM_004616.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:111336858 C>T maps to NM_152591.1 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr12:111336858 C>T maps to NM_152591.1 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr13:58208728 G>A maps to NM_001040429.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr13:58208728 G>A maps to NM_001040429.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr16:2025081 C>T maps to NM_006453.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr16:2025081 C>T maps to NM_006453.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr17:45471418 C>T maps to NM_152347.4 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr17:45471418 C>T maps to NM_152347.4 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr18:63547823 G>A maps to NM_004361.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr18:63547823 G>A maps to NM_004361.2 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr19:868169 C>T maps to NM_005481.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr19:868169 C>T maps to NM_005481.2 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr19:36303167 C>T maps to NM_021232.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr19:36303167 C>T maps to NM_021232.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr19:51330299 G>A maps to NM_017509.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr19:51330299 G>A maps to NM_017509.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:87073861 C>G maps to NM_172213.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:87073861 C>G maps to NM_172213.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:102644814 A>G maps to NM_004633.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:102644814 A>G maps to NM_004633.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:103040873 G>A maps to NM_003853.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:103040873 G>A maps to NM_003853.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:227660007 C>T maps to NM_005544.2 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr2:227660007 C>T maps to NM_005544.2 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr20:47591340 G>A maps to NM_006420.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr20:47591340 G>A maps to NM_006420.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr20:61596499 G>A maps to NM_022082.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr20:61596499 G>A maps to NM_022082.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr22:50860802 G>A maps to ENST00000216061 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr22:50860802 G>A maps to ENST00000216061 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr3:9802445 G>A maps to NM_003656.3 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr3:9802445 G>A maps to NM_003656.3 C213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr3:40457377 G>A maps to NM_001248.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr3:40457377 G>A maps to NM_001248.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr3:51418533 C>T maps to NM_004947.4 D1879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr3:51418533 C>T maps to NM_004947.4 D1879D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr4:167656161 A>G maps to NM_016950.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr4:167656161 A>G maps to NM_016950.2 D407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr6:44122463 G>A maps to NM_018426.1 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr6:44122463 G>A maps to NM_018426.1 V781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr6:84911453 C>G did not map to a codon.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr6:84911453 C>G did not map to a codon.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr7:43484402 G>A maps to NM_015052.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr7:43484402 G>A maps to NM_015052.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr7:80433420 C>G did not map to a codon.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr7:80433420 C>G did not map to a codon.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr7:82585981 A>G maps to NM_033026.5 D1429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr7:82585981 A>G maps to NM_033026.5 D1429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr8:144994984 G>A maps to NM_201380.2 R3139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chr8:144994984 G>A maps to NM_201380.2 R3139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chrX:123202506 G>T did not map to a codon.
Sequencing variant TCGA-32-5222-01A-01D-1486-08 chrX:123202506 G>T did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr1:179972354 G>A maps to NM_014810.4 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr1:179972354 G>A maps to NM_014810.4 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr10:73462358 T>C maps to ENST00000398860 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr10:73462358 T>C maps to ENST00000398860 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr10:105209446 G>A maps to NM_015916.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr10:105209446 G>A maps to NM_015916.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr11:60183724 T>C maps to NM_032597.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr11:60183724 T>C maps to NM_032597.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr11:94335055 C>T maps to NM_152431.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr11:94335055 C>T maps to NM_152431.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr12:96641079 C>T maps to NM_005230.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr12:96641079 C>T maps to NM_005230.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr16:30080983 C>T maps to ENST00000395248 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr16:30080983 C>T maps to ENST00000395248 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr17:914059 G>A maps to NM_021962.2 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr17:914059 G>A maps to NM_021962.2 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr17:48268237 G>T maps to NM_000088.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr17:48268237 G>T maps to NM_000088.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr18:43205721 C>T maps to NM_007163.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr18:43205721 C>T maps to NM_007163.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr19:50978583 G>A maps to ENST00000391816 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr19:50978583 G>A maps to ENST00000391816 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr2:45773869 C>A did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr2:45773869 C>A did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr20:15210607 A>T maps to ENST00000310348 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr20:15210607 A>T maps to ENST00000310348 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr22:23974204 C>T maps to NM_016449.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr22:23974204 C>T maps to NM_016449.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr22:30738318 C>T maps to NM_005877.4 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr22:30738318 C>T maps to NM_005877.4 W249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr3:53376298 C>A did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr3:53376298 C>A did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr4:38798600 G>A maps to NM_003263.3 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr4:38798600 G>A maps to NM_003263.3 Q618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr5:131039793 T>C maps to NM_133372.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr5:131039793 T>C maps to NM_133372.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr6:30458929 C>T maps to NM_005516.5 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr6:30458929 C>T maps to NM_005516.5 H209H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr6:70878103 T>A maps to NM_001858.4 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr6:70878103 T>A maps to NM_001858.4 P846P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr6:109481831 C>T maps to NM_173830.4 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr6:109481831 C>T maps to NM_173830.4 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr7:117864827 C>T did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr7:117864827 C>T did not map to a codon.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr8:38677274 T>C maps to ENST00000379931 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2571-01A-01D-1495-08 chr8:38677274 T>C maps to ENST00000379931 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:24465094 C>T maps to NM_021258.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:24465094 C>T maps to NM_021258.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:28477493 G>A maps to NM_001164721.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:28477493 G>A maps to NM_001164721.1 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:166888603 G>A maps to NM_199351.2 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:166888603 G>A maps to NM_199351.2 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:198676013 G>A maps to ENST00000271610 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr1:198676013 G>A maps to ENST00000271610 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr11:72945626 C>T maps to NM_176071.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr11:72945626 C>T maps to NM_176071.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr15:89389066 C>T maps to NM_013227.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr15:89389066 C>T maps to NM_013227.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr16:67477040 G>A maps to NM_004691.4 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr16:67477040 G>A maps to NM_004691.4 D174D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr17:5235421 T>G maps to NM_004703.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr17:5235421 T>G maps to NM_004703.4 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:746492 C>T maps to NM_002579.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:746492 C>T maps to NM_002579.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:37853830 G>A maps to NM_181786.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:37853830 G>A maps to NM_181786.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:53794412 G>A did not map to a codon.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:53794412 G>A did not map to a codon.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:54784354 G>A maps to ENST00000391747 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr19:54784354 G>A maps to ENST00000391747 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr2:24435599 C>T maps to NM_006277.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr2:24435599 C>T maps to NM_006277.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr2:155099238 C>T maps to NM_052917.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr2:155099238 C>T maps to NM_052917.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr20:42331497 G>A maps to NM_002466.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr20:42331497 G>A maps to NM_002466.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr3:13659762 C>T maps to NM_001165035.1 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr3:13659762 C>T maps to NM_001165035.1 D639D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-41-2572-01A-01D-1353-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-41-2572-01A-01D-1353-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr4:1161328 G>A maps to NM_012445.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr4:1161328 G>A maps to NM_012445.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr4:3251161 C>T maps to NM_001042690.1 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr4:3251161 C>T maps to NM_001042690.1 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr4:71691906 C>A maps to NM_002092.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr4:71691906 C>A maps to NM_002092.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr5:140720211 C>T maps to NM_018915.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr5:140720211 C>T maps to NM_018915.2 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr6:33036841 G>A maps to NM_033554.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr6:33036841 G>A maps to NM_033554.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr8:94713460 A>G maps to ENST00000452913 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr8:94713460 A>G maps to ENST00000452913 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr9:35092239 G>T maps to NM_032634.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chr9:35092239 G>T maps to NM_032634.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chrX:1584668 G>A maps to NM_178129.4 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chrX:1584668 G>A maps to NM_178129.4 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chrX:54986327 T>C did not map to a codon.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chrX:54986327 T>C did not map to a codon.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chrX:114248417 G>A maps to NM_000640.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2572-01A-01D-1353-08 chrX:114248417 G>A maps to NM_000640.2 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr1:21016726 A>G maps to NM_020816.2 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr1:21016726 A>G maps to NM_020816.2 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr11:4661910 T>A maps to NM_001004751.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr11:4661910 T>A maps to NM_001004751.2 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr12:6138531 G>A maps to NM_000552.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr12:6138531 G>A maps to NM_000552.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr12:9225467 C>A did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr12:9225467 C>A did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr12:39079419 C>A did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr12:39079419 C>A did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr15:33822867 G>A did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr15:33822867 G>A did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr16:74750317 C>T maps to NM_024306.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr16:74750317 C>T maps to NM_024306.4 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr17:10412801 C>T maps to NM_005963.3 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr17:10412801 C>T maps to NM_005963.3 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr17:58725370 A>T maps to NM_003620.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr17:58725370 A>T maps to NM_003620.3 G315G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-41-2573-01A-01D-1495-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-41-2573-01A-01D-1495-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-41-2573-01A-01D-1495-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-41-2573-01A-01D-1495-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr3:49064275 G>A maps to NM_000884.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr3:49064275 G>A maps to NM_000884.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr3:156763430 C>T maps to NM_001004316.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr3:156763430 C>T maps to NM_001004316.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr4:60029 A>T maps to NM_182524.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr4:60029 A>T maps to NM_182524.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr5:53751480 T>G did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr5:53751480 T>G did not map to a codon.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr5:56179394 G>A maps to NM_005921.1 P1236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr5:56179394 G>A maps to NM_005921.1 P1236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr6:29455046 G>A maps to NM_052967.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr6:29455046 G>A maps to NM_052967.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr6:130762227 C>T maps to NM_052913.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr6:130762227 C>T maps to NM_052913.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr8:42220140 A>G maps to NM_002690.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr8:42220140 A>G maps to NM_002690.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr8:145661199 G>A maps to NM_013432.4 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr8:145661199 G>A maps to NM_013432.4 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr9:137591839 C>T maps to NM_000093.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2573-01A-01D-1495-08 chr9:137591839 C>T maps to NM_000093.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr1:54605732 G>A maps to NM_201546.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr1:54605732 G>A maps to NM_201546.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr11:494708 G>A maps to NM_203389.1 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr11:494708 G>A maps to NM_203389.1 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr13:99061721 G>A maps to NM_005766.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr13:99061721 G>A maps to NM_005766.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr15:100591783 G>A maps to NM_139057.2 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr15:100591783 G>A maps to NM_139057.2 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr16:27374436 G>A maps to NM_000418.2 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr16:27374436 G>A maps to NM_000418.2 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:1303394 G>A maps to NM_006761.4 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:1303394 G>A maps to NM_006761.4 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:7577608 C>G did not map to a codon.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:7577608 C>G did not map to a codon.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:61950622 G>A maps to NM_020991.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:61950622 G>A maps to NM_020991.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:67077246 G>A maps to NM_080284.2 D1552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr17:67077246 G>A maps to NM_080284.2 D1552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr19:6828652 C>T maps to NM_005428.2 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr19:6828652 C>T maps to NM_005428.2 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr19:54848148 C>G maps to NM_012276.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr19:54848148 C>G maps to NM_012276.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr2:183597245 C>T maps to NM_018981.1 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr2:183597245 C>T maps to NM_018981.1 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr2:198950331 G>A maps to NM_006226.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr2:198950331 G>A maps to NM_006226.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr3:186362630 C>T maps to NM_014375.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr3:186362630 C>T maps to NM_014375.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr5:140768647 G>A maps to NM_003736.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr5:140768647 G>A maps to NM_003736.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr6:38805719 C>A maps to ENST00000327475 A1444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr6:38805719 C>A maps to ENST00000327475 A1444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr7:42977022 C>T maps to NM_031903.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr7:42977022 C>T maps to NM_031903.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr7:90895151 G>A maps to NM_003505.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr7:90895151 G>A maps to NM_003505.1 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr7:99705015 A>G maps to ENST00000472509 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr7:99705015 A>G maps to ENST00000472509 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr8:144996425 C>T maps to NM_201380.2 Q2658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-2575-01A-01D-1495-08 chr8:144996425 C>T maps to NM_201380.2 Q2658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:10221284 C>T maps to NM_001105562.2 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:10221284 C>T maps to NM_001105562.2 R1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:115828972 G>A maps to NM_002506.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:115828972 G>A maps to NM_002506.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:147380210 C>T maps to NM_005267.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:152278814 G>A maps to NM_002016.1 D2849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:152278814 G>A maps to NM_002016.1 D2849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:206760183 T>G maps to NM_182663.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr1:206760183 T>G maps to NM_182663.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr10:1263024 G>A maps to NM_018702.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr10:1263024 G>A maps to NM_018702.2 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr12:54369091 C>T maps to NM_014212.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr12:54369091 C>T maps to NM_014212.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr14:20665688 C>G maps to NM_001005503.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr14:20665688 C>G maps to NM_001005503.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr16:89256721 G>A maps to NM_004933.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr16:89256721 G>A maps to NM_004933.2 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr17:79080619 C>T maps to NM_017451.2 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr17:79080619 C>T maps to NM_017451.2 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr19:15728929 C>T maps to NM_007253.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr19:15728929 C>T maps to NM_007253.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr19:55603588 C>G did not map to a codon.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr19:55603588 C>G did not map to a codon.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr2:152580857 C>T maps to NM_001164507.1 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr2:152580857 C>T maps to NM_001164507.1 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr3:9825866 G>A maps to NM_006354.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr3:9825866 G>A maps to NM_006354.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr3:42602654 C>G maps to NM_032970.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr3:42602654 C>G maps to NM_032970.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr3:77147195 G>A maps to ENST00000332191 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr3:77147195 G>A maps to ENST00000332191 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr4:48490670 C>T maps to NM_152679.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr4:48490670 C>T maps to NM_152679.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr5:140012229 T>A maps to NM_001174105.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr5:140012229 T>A maps to NM_001174105.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr5:167420176 G>A maps to NM_001122679.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr5:167420176 G>A maps to NM_001122679.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr5:168149966 G>T maps to NM_003062.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr5:168149966 G>T maps to NM_003062.2 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr8:135622735 A>T maps to NM_020863.3 L204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chr8:135622735 A>T maps to NM_020863.3 L204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chrX:100169503 A>G maps to ENST00000328526 Y404Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chrX:100169503 A>G maps to ENST00000328526 Y404Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chrX:142718879 C>T maps to NM_001184749.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3392-01A-01D-1495-08 chrX:142718879 C>T maps to NM_001184749.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:3412514 G>A maps to ENST00000452816 C1345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:3412514 G>A maps to ENST00000452816 C1345C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:43909458 C>T maps to NM_015284.2 P2040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:43909458 C>T maps to NM_015284.2 P2040P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:91182335 C>T maps to NM_020063.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:91182335 C>T maps to NM_020063.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:151315094 G>C maps to NM_000449.3 S473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr1:151315094 G>C maps to NM_000449.3 S473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr12:50484022 G>A did not map to a codon.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr12:50484022 G>A did not map to a codon.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr12:55025621 T>C maps to NM_033277.1 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr12:55025621 T>C maps to NM_033277.1 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr2:163253350 G>A maps to NM_033272.2 R838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr2:163253350 G>A maps to NM_033272.2 R838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr2:192700729 G>A maps to NM_004657.5 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr2:192700729 G>A maps to NM_004657.5 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr20:3674184 G>A maps to NM_023068.3 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr20:3674184 G>A maps to NM_023068.3 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr22:40283671 G>A maps to NM_152512.3 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr22:40283671 G>A maps to NM_152512.3 N27N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr22:51063596 G>A maps to ENST00000395624 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr22:51063596 G>A maps to ENST00000395624 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr3:111901018 C>T maps to NM_183061.1 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr3:111901018 C>T maps to NM_183061.1 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr3:132390694 T>C maps to NM_024818.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr3:132390694 T>C maps to NM_024818.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr4:70822069 A>G maps to NM_001891.2 *227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr4:70822069 A>G maps to NM_001891.2 *227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr6:29080038 C>T maps to NM_001005216.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr6:29080038 C>T maps to NM_001005216.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr6:32041531 G>A maps to ENST00000375244 R1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr6:32041531 G>A maps to ENST00000375244 R1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:43484235 G>T maps to NM_015052.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:43484235 G>T maps to NM_015052.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:84727156 T>C maps to NM_152754.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:84727156 T>C maps to NM_152754.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:138764822 C>T maps to ENST00000464606 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:138764822 C>T maps to ENST00000464606 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:140154504 C>A maps to NM_013446.3 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr7:140154504 C>A maps to NM_013446.3 E421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr8:24181516 G>A did not map to a codon.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr8:24181516 G>A did not map to a codon.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr9:114332376 G>A maps to NM_001146108.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr9:114332376 G>A maps to NM_001146108.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr9:141012526 A>T maps to ENST00000277549 G1970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chr9:141012526 A>T maps to ENST00000277549 G1970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:1471116 C>T maps to NM_002183.2 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:1471116 C>T maps to NM_002183.2 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:9693806 G>C maps to ENST00000380929 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:9693806 G>C maps to ENST00000380929 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:102755507 G>A maps to NM_080879.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:102755507 G>A maps to NM_080879.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:105179165 C>T maps to NM_198465.2 Y1168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:105179165 C>T maps to NM_198465.2 Y1168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:132161936 G>A maps to NM_031907.1 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:132161936 G>A maps to NM_031907.1 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:134426219 A>G maps to NM_007131.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3393-01A-01D-1353-08 chrX:134426219 A>G maps to NM_007131.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr1:53099191 G>C maps to NM_001042693.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr1:53099191 G>C maps to NM_001042693.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr1:85592201 G>A maps to NM_145172.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr1:85592201 G>A maps to NM_145172.3 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr1:207643226 G>A maps to NM_001006658.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr1:207643226 G>A maps to NM_001006658.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr10:102789811 G>T maps to NM_001195263.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr10:102789811 G>T maps to NM_001195263.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr10:103827207 C>G maps to NM_024747.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr10:103827207 C>G maps to NM_024747.4 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr11:57156545 G>A maps to NM_002728.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr11:57156545 G>A maps to NM_002728.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr11:60184318 C>T maps to NM_032597.3 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr11:60184318 C>T maps to NM_032597.3 A626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr12:39268299 T>A maps to NM_153634.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr12:39268299 T>A maps to NM_153634.2 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr12:57324007 A>G did not map to a codon.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr12:57324007 A>G did not map to a codon.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr15:68118618 C>T maps to ENST00000380035 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr15:68118618 C>T maps to ENST00000380035 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr17:77758111 G>A maps to NM_005189.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr17:77758111 G>A maps to NM_005189.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr19:10625051 G>A maps to NM_001166215.1 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr19:10625051 G>A maps to NM_001166215.1 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr19:44223762 C>T maps to NM_019612.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr19:44223762 C>T maps to NM_019612.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr19:45515221 C>T maps to ENST00000221452 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr19:45515221 C>T maps to ENST00000221452 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr2:201332020 C>T maps to ENST00000409151 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr2:201332020 C>T maps to ENST00000409151 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr2:204320200 G>A maps to ENST00000374493 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr2:204320200 G>A maps to ENST00000374493 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr20:30193854 G>A did not map to a codon.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr20:30193854 G>A did not map to a codon.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr4:81504249 G>A maps to ENST00000508675 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr4:81504249 G>A maps to ENST00000508675 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr5:140588487 C>T maps to NM_018932.3 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr5:140588487 C>T maps to NM_018932.3 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr6:107391896 C>T maps to NM_001080450.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr6:107391896 C>T maps to NM_001080450.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr9:21141167 C>T maps to NM_002177.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr9:21141167 C>T maps to NM_002177.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr9:130674959 C>A did not map to a codon.
Sequencing variant TCGA-41-3915-01A-01D-1353-08 chr9:130674959 C>A did not map to a codon.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr1:237550597 C>T maps to NM_001035.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr1:237550597 C>T maps to NM_001035.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr11:27114718 C>T maps to NM_003986.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr11:27114718 C>T maps to NM_003986.2 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr11:45274268 C>A maps to NM_020826.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr11:45274268 C>A maps to NM_020826.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr11:123810625 C>T maps to NM_001001965.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr11:123810625 C>T maps to NM_001001965.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr15:76484331 G>A maps to NM_152335.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr15:76484331 G>A maps to NM_152335.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr16:31072649 C>T maps to NM_001172669.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr16:31072649 C>T maps to NM_001172669.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr17:29508777 C>G maps to NM_001042492.2 Y235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr17:29508777 C>G maps to NM_001042492.2 Y235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr2:21227176 G>A maps to NM_000384.2 D4017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr2:21227176 G>A maps to NM_000384.2 D4017D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr20:35060224 G>A maps to ENST00000339266 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr20:35060224 G>A maps to ENST00000339266 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr5:55210698 C>T maps to NM_139017.4 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr5:55210698 C>T maps to NM_139017.4 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr5:66462446 C>T maps to NM_001164664.1 S2480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr5:66462446 C>T maps to NM_001164664.1 S2480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr5:160047789 C>T maps to NM_025153.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr5:160047789 C>T maps to NM_025153.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:28228339 A>G maps to NM_001007531.1 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:28228339 A>G maps to NM_001007531.1 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:28333383 G>A maps to NM_024493.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:28333383 G>A maps to NM_024493.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:30671652 G>A maps to NM_014641.2 A1769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:30671652 G>A maps to NM_014641.2 A1769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:31584613 A>G maps to NM_001623.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr6:31584613 A>G maps to NM_001623.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr7:2613076 C>A maps to NM_152558.3 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr7:2613076 C>A maps to NM_152558.3 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr8:101018319 T>C maps to NM_015668.3 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr8:101018319 T>C maps to NM_015668.3 E793E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr9:107288581 T>C maps to NM_001001919.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chr9:107288581 T>C maps to NM_001001919.1 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chrX:70324147 C>T maps to ENST00000438526 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chrX:70324147 C>T maps to ENST00000438526 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chrX:123182853 G>T did not map to a codon.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chrX:123182853 G>T did not map to a codon.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chrX:142121935 G>A maps to ENST00000370504 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-4097-01A-01D-1353-08 chrX:142121935 G>A maps to ENST00000370504 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr1:40945131 G>A maps to NM_198494.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr1:40945131 G>A maps to NM_198494.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr1:152275877 C>T maps to NM_002016.1 S3828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr1:152275877 C>T maps to NM_002016.1 S3828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr11:3690463 G>A maps to NM_020402.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr11:3690463 G>A maps to NM_020402.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr11:12241779 G>A maps to NM_014632.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr11:12241779 G>A maps to NM_014632.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr11:103780459 G>A maps to NM_025208.4 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr11:103780459 G>A maps to NM_025208.4 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr12:57963410 G>A maps to NM_004984.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr12:57963410 G>A maps to NM_004984.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr12:58204640 G>A maps to NM_006576.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr12:58204640 G>A maps to NM_006576.3 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:23564496 G>A did not map to a codon.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:23564496 G>A did not map to a codon.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:23857465 G>C maps to NM_002471.3 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:23857465 G>C maps to NM_002471.3 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:74971517 C>T maps to NM_000428.2 V1472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:74971517 C>T maps to NM_000428.2 V1472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:81744721 T>G maps to NM_033104.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:81744721 T>G maps to NM_033104.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:94953696 G>A maps to NM_173850.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr14:94953696 G>A maps to NM_173850.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr15:52537562 G>A maps to NM_018728.3 H722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr15:52537562 G>A maps to NM_018728.3 H722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr16:67681848 C>T maps to NM_001013838.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr16:67681848 C>T maps to NM_001013838.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr17:62034851 C>T maps to NM_000334.4 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr17:62034851 C>T maps to NM_000334.4 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr19:9033636 G>A maps to NM_024690.2 N12100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr19:9033636 G>A maps to NM_024690.2 N12100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr19:11978930 T>C maps to NM_152262.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr19:11978930 T>C maps to NM_152262.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr19:41597755 G>A maps to NM_000766.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr19:41597755 G>A maps to NM_000766.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr2:103039782 C>T maps to NM_003853.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr2:103039782 C>T maps to NM_003853.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr2:215855593 C>T maps to NM_173076.2 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr2:215855593 C>T maps to NM_173076.2 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr2:234681030 C>T maps to ENST00000373460 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr2:234681030 C>T maps to ENST00000373460 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr20:50159017 C>T maps to NM_012340.3 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr20:50159017 C>T maps to NM_012340.3 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr20:62729400 C>T maps to NM_000913.3 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr20:62729400 C>T maps to NM_000913.3 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr21:41137663 C>T maps to NM_001080444.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr21:41137663 C>T maps to NM_001080444.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr21:46320381 G>A maps to NM_000211.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr21:46320381 G>A maps to NM_000211.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr22:30856049 G>A maps to NM_174975.4 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr22:30856049 G>A maps to NM_174975.4 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr3:52020669 T>C maps to ENST00000463937 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr3:52020669 T>C maps to ENST00000463937 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr4:13481053 C>A maps to NM_004249.3 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr4:13481053 C>A maps to NM_004249.3 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr5:77784734 C>G maps to NM_005779.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr5:77784734 C>G maps to NM_005779.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr5:167551888 A>G maps to NM_001122679.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr5:167551888 A>G maps to NM_001122679.1 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr6:39159463 C>A maps to NM_003740.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr6:39159463 C>A maps to NM_003740.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr7:31014609 C>T maps to NM_000823.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr7:31014609 C>T maps to NM_000823.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr7:92765182 C>T maps to NM_152703.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr7:92765182 C>T maps to NM_152703.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr8:24199260 C>T maps to NM_014265.4 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr8:24199260 C>T maps to NM_014265.4 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr8:120977650 G>T did not map to a codon.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr8:120977650 G>T did not map to a codon.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr9:90220081 C>T maps to NM_004938.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr9:90220081 C>T maps to NM_004938.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr9:125239494 G>A maps to NM_001004451.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chr9:125239494 G>A maps to NM_001004451.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chrX:3235172 C>T maps to NM_015419.3 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chrX:3235172 C>T maps to NM_015419.3 P2183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chrX:30577749 C>T maps to NM_025159.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chrX:30577749 C>T maps to NM_025159.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chrX:70613221 A>C maps to ENST00000449580 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-5651-01A-01D-1696-08 chrX:70613221 A>C maps to ENST00000449580 G1040G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr1:179886765 C>T maps to ENST00000398836 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr1:179886765 C>T maps to ENST00000398836 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr1:183087213 T>C maps to NM_002293.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr1:183087213 T>C maps to NM_002293.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr10:21185901 C>T maps to ENST00000430741 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr10:21185901 C>T maps to ENST00000430741 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr11:58722268 C>A maps to NM_080661.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr11:58722268 C>A maps to NM_080661.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr11:66192331 C>T maps to NM_178864.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr11:66192331 C>T maps to NM_178864.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr12:21643133 A>G maps to NM_032941.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr12:21643133 A>G maps to NM_032941.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr17:29654690 C>T maps to NM_001042492.2 Q1815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr17:29654690 C>T maps to NM_001042492.2 Q1815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr2:110922206 G>A maps to NM_000272.3 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr2:110922206 G>A maps to NM_000272.3 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr2:133547631 G>A maps to NM_207363.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr2:133547631 G>A maps to NM_207363.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr2:173356004 C>T maps to ENST00000264106 D984D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr2:173356004 C>T maps to ENST00000264106 D984D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr21:19687505 G>A maps to NM_002772.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr21:19687505 G>A maps to NM_002772.2 D663D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr22:32445980 C>T maps to NM_000343.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr22:32445980 C>T maps to NM_000343.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr3:89478301 G>A maps to NM_005233.5 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr3:89478301 G>A maps to NM_005233.5 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr4:37962336 C>T maps to NM_006607.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr4:37962336 C>T maps to NM_006607.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr4:168155200 T>A maps to NM_016950.2 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr4:168155200 T>A maps to NM_016950.2 K42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr6:31637271 C>T maps to ENST00000375885 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr6:31637271 C>T maps to ENST00000375885 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr9:111822725 T>A maps to NM_032012.3 K544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-41-6646-01A-11D-1845-08 chr9:111822725 T>A maps to NM_032012.3 K544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr1:114354434 G>C maps to NM_018364.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr1:114354434 G>C maps to NM_018364.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr11:31531363 C>G maps to ENST00000395934 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr11:31531363 C>G maps to ENST00000395934 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr19:7120677 T>C maps to NM_000208.2 A1204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr19:7120677 T>C maps to NM_000208.2 A1204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr19:54140038 C>T maps to NM_001012728.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr19:54140038 C>T maps to NM_001012728.1 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr2:170163789 C>T did not map to a codon.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr2:170163789 C>T did not map to a codon.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr22:38120287 C>T maps to NM_001039141.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr22:38120287 C>T maps to NM_001039141.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr3:51315130 C>T maps to NM_004947.4 H923H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr3:51315130 C>T maps to NM_004947.4 H923H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr3:168833247 G>A maps to NM_004991.3 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr3:168833247 G>A maps to NM_004991.3 N804N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr4:6062186 G>A maps to NM_001099433.1 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr4:6062186 G>A maps to NM_001099433.1 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr4:8089917 C>T maps to NM_001130083.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr4:8089917 C>T maps to NM_001130083.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr5:149501488 G>T maps to NM_002609.3 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr5:149501488 G>T maps to NM_002609.3 I766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr6:17805707 C>A maps to NM_022113.4 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr6:17805707 C>A maps to NM_022113.4 E768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr7:99955937 C>T maps to ENST00000413850 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr7:99955937 C>T maps to ENST00000413850 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr7:151097265 G>A maps to ENST00000426624 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chr7:151097265 G>A maps to ENST00000426624 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chrX:84363107 C>T maps to NM_001012980.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6573-01A-12D-1845-08 chrX:84363107 C>T maps to NM_001012980.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:100464898 A>C maps to ENST00000370153 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:100464898 A>C maps to ENST00000370153 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:151820731 G>A maps to NM_182578.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:151820731 G>A maps to NM_182578.3 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:182898837 T>A maps to ENST00000287709 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:182898837 T>A maps to ENST00000287709 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:248263534 C>A maps to NM_175911.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr1:248263534 C>A maps to NM_175911.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:556904 C>T maps to NM_173573.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:556904 C>T maps to NM_173573.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:1156627 C>T maps to ENST00000406844 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:1156627 C>T maps to ENST00000406844 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:120998518 C>T maps to NM_005422.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:120998518 C>T maps to NM_005422.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:121031073 G>A maps to NM_005422.2 P1640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr11:121031073 G>A maps to NM_005422.2 P1640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr15:58957379 G>A maps to NM_001110.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr15:58957379 G>A maps to NM_001110.2 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr17:67211982 A>G maps to NM_080282.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr17:67211982 A>G maps to NM_080282.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr18:19996610 G>A maps to NM_172241.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr18:19996610 G>A maps to NM_172241.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr18:34854356 G>A maps to NM_020180.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr18:34854356 G>A maps to NM_020180.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:288136 G>A maps to NM_177543.1 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:288136 G>A maps to NM_177543.1 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:2733312 C>T maps to NM_144564.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:2733312 C>T maps to NM_144564.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:6854016 C>T maps to NM_005428.2 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:6854016 C>T maps to NM_005428.2 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:17014388 G>A maps to ENST00000443236 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:17014388 G>A maps to ENST00000443236 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:19206998 G>T maps to NM_178526.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:19206998 G>T maps to NM_178526.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:44015697 G>A maps to NM_014297.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:44015697 G>A maps to NM_014297.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:51503468 A>G maps to NM_144505.1 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:51503468 A>G maps to NM_144505.1 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:55377846 G>A maps to ENST00000355608 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:55377846 G>A maps to ENST00000355608 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:56313011 C>G maps to NM_145007.3 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr19:56313011 C>G maps to NM_145007.3 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr2:71576266 T>C maps to NM_014497.3 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr2:71576266 T>C maps to NM_014497.3 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr2:178481797 G>A maps to NM_152275.3 C544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr2:178481797 G>A maps to NM_152275.3 C544C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr2:234628245 C>T maps to NM_007120.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr2:234628245 C>T maps to NM_007120.2 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr3:10301999 G>A maps to NM_014760.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr3:10301999 G>A maps to NM_014760.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr3:194062051 G>A maps to NM_001080513.2 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr3:194062051 G>A maps to NM_001080513.2 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr4:79236805 T>G maps to NM_025074.6 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr4:79236805 T>G maps to NM_025074.6 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:36677193 G>C maps to NM_004172.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:36677193 G>C maps to NM_004172.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:94044305 T>A maps to NM_024717.4 K947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:94044305 T>A maps to NM_024717.4 K947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:140307514 G>A maps to NM_018898.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:140307514 G>A maps to NM_018898.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:140778095 G>A maps to NM_018925.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr5:140778095 G>A maps to NM_018925.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr7:80374223 A>G maps to NM_006379.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr7:80374223 A>G maps to NM_006379.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr7:86521206 T>A did not map to a codon.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr7:86521206 T>A did not map to a codon.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr7:131865368 G>A maps to NM_020911.1 N1205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr7:131865368 G>A maps to NM_020911.1 N1205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr9:15214138 G>C maps to NM_152574.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr9:15214138 G>C maps to NM_152574.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr9:112200416 G>A maps to NM_002829.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr9:112200416 G>A maps to NM_002829.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr9:134394273 C>T maps to NM_007171.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chr9:134394273 C>T maps to NM_007171.3 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:1407533 A>G maps to NM_001161530.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:1407533 A>G maps to NM_001161530.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:15526511 C>G maps to NM_203281.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:15526511 C>G maps to NM_203281.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:18664127 C>T maps to NM_001037343.1 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:18664127 C>T maps to NM_001037343.1 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:108868078 G>A maps to NM_012282.2 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:108868078 G>A maps to NM_012282.2 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:153592698 G>A maps to NM_001110556.1 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6575-01A-11D-1845-08 chrX:153592698 G>A maps to NM_001110556.1 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr14:24779986 C>A maps to ENST00000336557 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr14:24779986 C>A maps to ENST00000336557 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr15:40750941 G>A maps to NM_014952.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr15:40750941 G>A maps to NM_014952.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr16:5058450 G>A maps to NM_014692.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr16:5058450 G>A maps to NM_014692.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr19:10335446 G>A maps to NM_004230.3 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr19:10335446 G>A maps to NM_004230.3 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr3:52475333 C>T maps to NM_020163.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr3:52475333 C>T maps to NM_020163.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr5:32774857 C>T maps to ENST00000265074 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr5:32774857 C>T maps to ENST00000265074 Y368Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr5:146750221 G>A maps to NM_001112724.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr5:146750221 G>A maps to NM_001112724.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr7:47869691 C>T maps to NM_138295.3 L2168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr7:47869691 C>T maps to NM_138295.3 L2168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr9:118982396 T>C maps to NM_002581.3 H700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chr9:118982396 T>C maps to NM_002581.3 H700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chrX:123197783 C>G maps to NM_001042750.1 Y636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6577-01A-11D-1845-08 chrX:123197783 C>G maps to NM_001042750.1 Y636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:32650217 G>A did not map to a codon.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:32650217 G>A did not map to a codon.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:39913452 G>A maps to ENST00000361689 Q4558Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:39913452 G>A maps to ENST00000361689 Q4558Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:120512132 C>T did not map to a codon.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:120512132 C>T did not map to a codon.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:229772129 C>A maps to NM_014777.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr1:229772129 C>A maps to NM_014777.2 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr11:122945483 G>A maps to NM_024769.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr11:122945483 G>A maps to NM_024769.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr11:134048750 C>T maps to NM_015261.2 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr11:134048750 C>T maps to NM_015261.2 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr12:32977044 G>A maps to NM_004572.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr12:32977044 G>A maps to NM_004572.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr12:109509448 G>A maps to NM_032663.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr12:109509448 G>A maps to NM_032663.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr19:49261317 A>C maps to NM_019113.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr19:49261317 A>C maps to NM_019113.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr19:54758760 C>T maps to NM_001081442.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr19:54758760 C>T maps to NM_001081442.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr2:208632194 G>A maps to NM_003468.3 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr2:208632194 G>A maps to NM_003468.3 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr20:16721055 T>C maps to NM_198220.2 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr20:16721055 T>C maps to NM_198220.2 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr20:21377635 G>A maps to NM_033176.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr20:21377635 G>A maps to NM_033176.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr21:10906910 G>A maps to NM_199261.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr21:10906910 G>A maps to NM_199261.2 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr22:46932242 G>A maps to NM_014246.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr22:46932242 G>A maps to NM_014246.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr3:38153749 T>C maps to NM_007335.2 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr3:38153749 T>C maps to NM_007335.2 P1188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr3:38591817 G>A maps to NM_001099404.1 I2015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr3:38591817 G>A maps to NM_001099404.1 I2015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr3:69120762 C>T maps to NM_003968.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr3:69120762 C>T maps to NM_003968.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr4:38830188 C>T maps to NM_006068.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr4:38830188 C>T maps to NM_006068.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr6:7575559 G>A maps to NM_004415.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr6:7575559 G>A maps to NM_004415.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr6:70961987 G>A maps to NM_001851.4 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr6:70961987 G>A maps to NM_001851.4 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr7:94039078 C>T maps to NM_000089.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr7:94039078 C>T maps to NM_000089.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr8:42939876 C>T maps to NM_002027.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr8:42939876 C>T maps to NM_002027.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr8:125131868 G>A maps to NM_001039112.2 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr8:125131868 G>A maps to NM_001039112.2 S1804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr9:140327979 C>T maps to NM_006647.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6578-01A-11D-1845-08 chr9:140327979 C>T maps to NM_006647.1 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr1:3687984 C>T maps to NM_152492.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr1:3687984 C>T maps to NM_152492.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr10:105906077 A>G maps to ENST00000389588 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr10:105906077 A>G maps to ENST00000389588 S1267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr11:408154 G>A maps to NM_021805.2 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr11:408154 G>A maps to NM_021805.2 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr11:103908617 G>A maps to NM_001001711.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr11:103908617 G>A maps to NM_001001711.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr13:111084707 G>A did not map to a codon.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr13:111084707 G>A did not map to a codon.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr15:44106721 G>T maps to NM_005926.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr15:44106721 G>T maps to NM_005926.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr16:31004531 G>A maps to NM_052874.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr16:31004531 G>A maps to NM_052874.3 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr19:54313742 G>A maps to ENST00000391773 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr19:54313742 G>A maps to ENST00000391773 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr20:3128198 A>C maps to NM_021826.4 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr20:3128198 A>C maps to NM_021826.4 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr3:151545689 A>G maps to NM_001086.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr3:151545689 A>G maps to NM_001086.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr4:146791484 G>A maps to ENST00000508784 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr4:146791484 G>A maps to ENST00000508784 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr5:55203286 C>T maps to NM_139017.4 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr5:55203286 C>T maps to NM_139017.4 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr6:27419108 T>C maps to NM_007149.2 K743K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chr6:27419108 T>C maps to NM_007149.2 K743K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-74-6584-01A-11D-1845-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-74-6584-01A-11D-1845-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chrX:27999268 G>A maps to NM_001017930.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-74-6584-01A-11D-1845-08 chrX:27999268 G>A maps to NM_001017930.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr1:45807216 C>G maps to NM_025077.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr1:45807216 C>G maps to NM_025077.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr1:156849918 G>A maps to NM_002529.3 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr1:156849918 G>A maps to NM_002529.3 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr1:161094313 G>A did not map to a codon.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr1:161094313 G>A did not map to a codon.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr10:88703547 G>A maps to NM_024756.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr10:88703547 G>A maps to NM_024756.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr11:7960953 G>A maps to NM_001003745.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr11:7960953 G>A maps to NM_001003745.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr16:81891937 G>A maps to NM_002661.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr16:81891937 G>A maps to NM_002661.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr19:19576171 C>T maps to ENST00000404158 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr19:19576171 C>T maps to ENST00000404158 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr19:39908645 C>G maps to NM_022835.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr19:39908645 C>G maps to NM_022835.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr19:51453307 G>A maps to NM_012427.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr19:51453307 G>A maps to NM_012427.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr3:64527057 G>A maps to NM_182920.1 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr3:64527057 G>A maps to NM_182920.1 P1775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr3:74334528 C>T maps to NM_020872.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr3:74334528 C>T maps to NM_020872.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr3:119373375 C>T maps to NM_022135.2 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr3:119373375 C>T maps to NM_022135.2 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr4:100805283 T>G did not map to a codon.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr4:100805283 T>G did not map to a codon.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr5:32255875 T>C did not map to a codon.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr5:32255875 T>C did not map to a codon.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr5:135692994 C>T maps to NM_020389.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr5:135692994 C>T maps to NM_020389.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr5:140182971 C>T maps to NM_018906.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr5:140182971 C>T maps to NM_018906.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:29539564 G>A maps to NM_004067.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:29539564 G>A maps to NM_004067.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:73472021 G>A maps to ENST00000358929 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:73472021 G>A maps to ENST00000358929 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:126882859 A>G maps to NM_001127323.1 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:126882859 A>G maps to NM_001127323.1 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:142625187 G>A maps to NM_019841.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:142625187 G>A maps to NM_019841.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:151944989 T>C maps to ENST00000355193 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr7:151944989 T>C maps to ENST00000355193 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr9:130605417 G>A maps to NM_001114753.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chr9:130605417 G>A maps to NM_001114753.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chrX:134156180 C>T maps to NM_001078173.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4925-01A-01D-1486-08 chrX:134156180 C>T maps to NM_001078173.1 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr1:1412699 G>A maps to NM_031921.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr1:1412699 G>A maps to NM_031921.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr1:2524280 G>A maps to NM_033467.3 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr1:2524280 G>A maps to NM_033467.3 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr10:24893239 C>T did not map to a codon.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr10:24893239 C>T did not map to a codon.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr11:118014755 C>T maps to NM_174934.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr11:118014755 C>T maps to NM_174934.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr11:118404797 C>T maps to NM_032780.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr11:118404797 C>T maps to NM_032780.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr12:53663688 C>T maps to NM_012291.4 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr12:53663688 C>T maps to NM_012291.4 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr15:81627092 G>A maps to ENST00000454937 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr15:81627092 G>A maps to ENST00000454937 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr19:18870985 C>T maps to NM_001098482.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr19:18870985 C>T maps to NM_001098482.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr2:179438087 A>G maps to NM_133378.4 Y21689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr2:179438087 A>G maps to NM_133378.4 Y21689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr22:50615938 C>T maps to NM_052839.3 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr22:50615938 C>T maps to NM_052839.3 D266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr4:79421049 G>A maps to NM_025074.6 K3097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr4:79421049 G>A maps to NM_025074.6 K3097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr4:159533467 C>T maps to ENST00000440678 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr4:159533467 C>T maps to ENST00000440678 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr5:1244837 C>T maps to NM_182632.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr5:1244837 C>T maps to NM_182632.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr6:26508919 A>C maps to NM_001732.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr6:26508919 A>C maps to NM_001732.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr6:50740519 C>T maps to NM_172238.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr6:50740519 C>T maps to NM_172238.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr8:104898338 C>T maps to NM_001100117.2 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr8:104898338 C>T maps to NM_001100117.2 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr9:16435842 G>A maps to NM_017637.5 Y783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr9:16435842 G>A maps to NM_017637.5 Y783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr9:141012522 C>G maps to ENST00000277549 S1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4926-01B-01D-1486-08 chr9:141012522 C>G maps to ENST00000277549 S1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr1:7797313 G>A did not map to a codon.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr1:7797313 G>A did not map to a codon.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr1:147380444 C>T maps to NM_005267.4 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr1:147380444 C>T maps to NM_005267.4 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr1:232144582 C>T maps to NM_001164537.1 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr1:232144582 C>T maps to NM_001164537.1 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr11:66189953 C>T maps to NM_178864.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr11:66189953 C>T maps to NM_178864.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr12:104721415 G>A maps to NM_001093771.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr12:104721415 G>A maps to NM_001093771.1 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr14:31142540 T>C maps to ENST00000311943 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr14:31142540 T>C maps to ENST00000311943 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr14:73729313 C>T maps to ENST00000427855 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr14:73729313 C>T maps to ENST00000427855 G834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr16:69148325 C>T maps to NM_005329.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr16:69148325 C>T maps to NM_005329.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:6420482 C>T did not map to a codon.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:6420482 C>T did not map to a codon.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:17375060 A>C maps to NM_031941.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:17375060 A>C maps to NM_031941.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:40872765 C>T maps to NM_012268.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:40872765 C>T maps to NM_012268.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:43372475 T>A maps to NM_006905.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:43372475 T>A maps to NM_006905.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:57088759 C>T maps to NM_001001668.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr19:57088759 C>T maps to NM_001001668.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr2:24246494 C>T maps to ENST00000338315 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr2:24246494 C>T maps to ENST00000338315 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr20:44841696 G>A maps to NM_021248.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr20:44841696 G>A maps to NM_021248.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr3:14862434 C>T maps to NM_152536.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr3:14862434 C>T maps to NM_152536.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr3:111603532 A>C maps to NM_001134438.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr3:111603532 A>C maps to NM_001134438.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr4:77818024 G>A maps to NM_001029870.1 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr4:77818024 G>A maps to NM_001029870.1 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr5:163558 G>A maps to NM_052909.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr5:163558 G>A maps to NM_052909.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:1522257 C>T maps to ENST00000389470 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:1522257 C>T maps to ENST00000389470 S1376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:37890337 G>A did not map to a codon.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:37890337 G>A did not map to a codon.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:97364144 C>T maps to NM_003182.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:97364144 C>T maps to NM_003182.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:156556438 C>T maps to ENST00000354505 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:156556438 C>T maps to ENST00000354505 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chrX:142717982 T>A maps to NM_001184749.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chrX:142717982 T>A maps to NM_001184749.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr1:6184050 G>C maps to NM_015557.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr1:6184050 G>C maps to NM_015557.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr1:45797966 C>T maps to NM_001128425.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr1:45797966 C>T maps to NM_001128425.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr10:128974484 G>A maps to NM_001039762.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr10:128974484 G>A maps to NM_001039762.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr11:25100152 A>G maps to NM_001009909.2 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr11:25100152 A>G maps to NM_001009909.2 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr13:25263440 G>A maps to NM_001185085.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr13:25263440 G>A maps to NM_001185085.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr14:77948977 G>A maps to NM_199296.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr14:77948977 G>A maps to NM_199296.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr16:9857170 C>T maps to NM_000833.3 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr16:9857170 C>T maps to NM_000833.3 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr17:40837034 G>A maps to NM_003632.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr17:40837034 G>A maps to NM_003632.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr18:44260034 G>A maps to NM_013305.4 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr18:44260034 G>A maps to NM_013305.4 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr19:56539656 C>T maps to NM_153447.4 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr19:56539656 C>T maps to NM_153447.4 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr20:36687858 C>T maps to NM_021215.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr20:36687858 C>T maps to NM_021215.3 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr3:168849256 G>A maps to NM_004991.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr3:168849256 G>A maps to NM_004991.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr3:182870189 G>A maps to NM_014398.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr3:182870189 G>A maps to NM_014398.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr3:194373562 C>T maps to NM_018385.2 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr3:194373562 C>T maps to NM_018385.2 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr4:74364953 T>A maps to NM_001133.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr4:74364953 T>A maps to NM_001133.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr4:88091237 G>A maps to NM_020803.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr4:88091237 G>A maps to NM_020803.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr4:166964453 T>C maps to ENST00000507499 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr4:166964453 T>C maps to ENST00000507499 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr5:136314405 G>A maps to NM_004598.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr5:136314405 G>A maps to NM_004598.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr5:140531523 G>A maps to NM_018939.2 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr5:140531523 G>A maps to NM_018939.2 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:63709525 C>A maps to NM_153363.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:63709525 C>A maps to NM_153363.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:99821642 G>A maps to NM_178831.6 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:99821642 G>A maps to NM_178831.6 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:112129962 C>T maps to NM_182597.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:112129962 C>T maps to NM_182597.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:131817921 G>A maps to NM_020911.1 S1825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:131817921 G>A maps to NM_020911.1 S1825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:148288175 C>T maps to NM_145304.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4928-01B-01D-1486-08 chr7:148288175 C>T maps to NM_145304.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:1147003 C>T maps to NM_003327.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:1147003 C>T maps to NM_003327.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:160162638 A>T maps to NM_001231.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:160162638 A>T maps to NM_001231.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:173010532 G>A maps to NM_005092.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:173010532 G>A maps to NM_005092.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:197887087 C>T maps to NM_020204.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr1:197887087 C>T maps to NM_020204.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr10:64564911 C>T maps to NM_032804.5 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr10:64564911 C>T maps to NM_032804.5 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr10:104934622 G>A maps to NM_001134373.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr10:104934622 G>A maps to NM_001134373.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr12:117962679 C>T maps to ENST00000339824 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr12:117962679 C>T maps to ENST00000339824 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr16:54967469 C>T maps to NM_005853.5 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr16:54967469 C>T maps to NM_005853.5 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr16:78064623 C>T maps to NM_005752.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr16:78064623 C>T maps to NM_005752.3 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:8170744 G>A maps to NM_012393.2 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:8170744 G>A maps to NM_012393.2 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:39661388 G>A maps to NM_153490.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:39661388 G>A maps to NM_153490.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:43320636 C>T maps to NM_005892.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr17:43320636 C>T maps to NM_005892.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr19:10405101 C>A maps to NM_003259.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr19:10405101 C>A maps to NM_003259.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr2:219254612 C>T maps to NM_000578.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr2:219254612 C>T maps to NM_000578.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr22:17450831 C>T did not map to a codon.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr22:17450831 C>T did not map to a codon.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr22:32234827 C>T maps to NM_001136029.1 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr22:32234827 C>T maps to NM_001136029.1 R829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr3:49737156 C>T maps to NM_022064.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr3:49737156 C>T maps to NM_022064.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr3:183962403 G>A maps to NM_005787.5 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr3:183962403 G>A maps to NM_005787.5 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr4:55131089 A>G maps to NM_006206.4 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr4:55131089 A>G maps to NM_006206.4 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr4:62363022 G>A maps to ENST00000506720 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr4:62363022 G>A maps to ENST00000506720 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr4:79507427 C>T maps to NM_005139.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr4:79507427 C>T maps to NM_005139.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr5:17275369 C>T maps to NM_006317.3 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr5:17275369 C>T maps to NM_006317.3 N15N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr9:5185458 G>A maps to NM_007179.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr9:5185458 G>A maps to NM_007179.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr9:88633636 T>C maps to NM_024635.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chr9:88633636 T>C maps to NM_024635.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:2799205 G>A maps to NM_003918.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:2799205 G>A maps to NM_003918.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:3229253 G>A maps to NM_015419.3 V2330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:3229253 G>A maps to NM_015419.3 V2330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:29972738 A>G maps to NM_014271.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:29972738 A>G maps to NM_014271.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:100117738 G>A maps to NM_007052.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:100117738 G>A maps to NM_007052.4 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:102004876 C>T maps to NM_001142530.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4929-01A-01D-1486-08 chrX:102004876 C>T maps to NM_001142530.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:153043126 G>A maps to NM_001017418.1 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:153043126 G>A maps to NM_001017418.1 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:154542047 C>T maps to NM_000748.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:154542047 C>T maps to NM_000748.2 Q59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:228564848 A>G maps to NM_001098623.1 A7712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:228564848 A>G maps to NM_001098623.1 A7712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:238050694 A>G maps to NM_021186.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr1:238050694 A>G maps to NM_021186.3 T240T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-76-4931-01A-01D-1486-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-76-4931-01A-01D-1486-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr10:89712006 G>T maps to NM_000314.4 G209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr10:89712006 G>T maps to NM_000314.4 G209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr10:112350787 G>A maps to NM_005445.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr10:112350787 G>A maps to NM_005445.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr11:35747530 G>A maps to NM_017583.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr11:35747530 G>A maps to NM_017583.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr11:60183895 G>A maps to NM_032597.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr11:60183895 G>A maps to NM_032597.3 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr11:93778979 G>A maps to NM_001098672.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr11:93778979 G>A maps to NM_001098672.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr12:31545305 G>A maps to NM_144973.3 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr12:31545305 G>A maps to NM_144973.3 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr14:88431915 G>A maps to NM_000153.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr14:88431915 G>A maps to NM_000153.2 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr15:73562539 G>A maps to NM_002499.3 W895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr15:73562539 G>A maps to NM_002499.3 W895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr17:39506773 C>T maps to NM_004138.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr17:39506773 C>T maps to NM_004138.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr18:74153648 G>A maps to ENST00000443185 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr18:74153648 G>A maps to ENST00000443185 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr19:1005284 C>T maps to NM_138690.1 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr19:1005284 C>T maps to NM_138690.1 Y595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr2:64863693 C>T maps to NM_014755.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr2:64863693 C>T maps to NM_014755.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr2:179474027 G>A maps to NM_133378.4 R14769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr2:179474027 G>A maps to NM_133378.4 R14769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr22:24579585 C>T maps to NM_019601.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr22:24579585 C>T maps to NM_019601.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr5:140590122 C>T maps to NM_018932.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr5:140590122 C>T maps to NM_018932.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr7:1485030 C>T maps to NM_182924.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr7:1485030 C>T maps to NM_182924.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr7:106508431 G>A maps to NM_002649.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr7:106508431 G>A maps to NM_002649.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr8:39613417 G>A maps to NM_001464.3 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chr8:39613417 G>A maps to NM_001464.3 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chrX:2799103 C>T maps to NM_003918.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chrX:2799103 C>T maps to NM_003918.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chrX:15266988 C>A maps to NM_001031739.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4931-01A-01D-1486-08 chrX:15266988 C>A maps to NM_001031739.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr1:152281685 G>A maps to NM_002016.1 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr1:152281685 G>A maps to NM_002016.1 A1892A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr1:213181755 C>T maps to NM_144567.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr1:213181755 C>T maps to NM_144567.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr11:56058034 G>A maps to NM_001005199.1 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr11:56058034 G>A maps to NM_001005199.1 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr12:47163174 G>A maps to NM_018018.4 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr12:47163174 G>A maps to NM_018018.4 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr12:111322002 G>A maps to NM_152591.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr12:111322002 G>A maps to NM_152591.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr13:31232151 A>G maps to NM_005800.4 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr13:31232151 A>G maps to NM_005800.4 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr19:54782294 C>T maps to ENST00000391747 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr19:54782294 C>T maps to ENST00000391747 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr2:135958007 T>C maps to NM_032143.2 R1048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr2:135958007 T>C maps to NM_032143.2 R1048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr2:180810269 A>G maps to NM_020943.2 N771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr2:180810269 A>G maps to NM_020943.2 N771N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr2:223161798 C>T maps to NM_181459.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr2:223161798 C>T maps to NM_181459.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr20:54824648 G>C maps to ENST00000371389 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr20:54824648 G>C maps to ENST00000371389 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr20:55093242 C>G maps to ENST00000357348 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr20:55093242 C>G maps to ENST00000357348 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr21:45948410 G>A maps to ENST00000443468 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr21:45948410 G>A maps to ENST00000443468 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr22:50596601 C>T maps to NM_018995.2 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr22:50596601 C>T maps to NM_018995.2 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr4:57237646 G>C maps to NM_181806.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr4:57237646 G>C maps to NM_181806.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr5:23527429 G>T maps to NM_020227.2 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr5:23527429 G>T maps to NM_020227.2 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr5:140719023 A>G maps to NM_018915.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr5:140719023 A>G maps to NM_018915.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr6:49976856 G>A maps to NM_001037728.2 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr6:49976856 G>A maps to NM_001037728.2 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr6:138599741 G>A maps to NM_020340.4 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr6:138599741 G>A maps to NM_020340.4 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr7:45956871 G>A maps to NM_001013398.1 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr7:45956871 G>A maps to NM_001013398.1 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr7:93519455 C>T maps to NM_006528.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr7:93519455 C>T maps to NM_006528.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr9:35808663 C>T maps to NM_003995.3 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4932-01A-01D-1486-08 chr9:35808663 C>T maps to NM_003995.3 R957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr10:18276537 C>T maps to NM_001145195.1 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr10:18276537 C>T maps to NM_001145195.1 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr11:5878740 A>G maps to NM_001005168.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr11:5878740 A>G maps to NM_001005168.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr11:5878764 C>T maps to NM_001005168.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr11:5878764 C>T maps to NM_001005168.1 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr12:53011873 G>A maps to NM_175068.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr12:53011873 G>A maps to NM_175068.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr12:57581168 G>T maps to NM_002332.2 E2321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr12:57581168 G>T maps to NM_002332.2 E2321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr12:59274531 A>G maps to NM_153377.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr12:59274531 A>G maps to NM_153377.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr16:88688689 C>T maps to ENST00000452588 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr16:88688689 C>T maps to ENST00000452588 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr17:39766791 C>T maps to NM_005557.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr17:39766791 C>T maps to NM_005557.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr2:39515366 C>A maps to NM_003618.2 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr2:39515366 C>A maps to NM_003618.2 G457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr2:121726341 G>A maps to NM_005270.4 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr2:121726341 G>A maps to NM_005270.4 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr2:242065779 C>T maps to ENST00000358649 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr2:242065779 C>T maps to ENST00000358649 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr20:44750989 C>T maps to NM_001250.4 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr20:44750989 C>T maps to NM_001250.4 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr22:50307404 T>C maps to NM_024105.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr22:50307404 T>C maps to NM_024105.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr3:150387204 C>T maps to NM_152394.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr3:150387204 C>T maps to NM_152394.3 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr4:55561741 A>G maps to NM_000222.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr4:55561741 A>G maps to NM_000222.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr4:156634552 C>T maps to NM_001130684.1 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr4:156634552 C>T maps to NM_001130684.1 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr5:118324198 G>T maps to NM_173666.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr5:118324198 G>T maps to NM_173666.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr5:140202967 G>A maps to NM_018908.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr5:140202967 G>A maps to NM_018908.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr8:17726235 G>A maps to NM_201552.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chr8:17726235 G>A maps to NM_201552.1 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chrX:49065813 G>T maps to NM_005183.2 R1632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4934-01A-01D-1486-08 chrX:49065813 G>T maps to NM_005183.2 R1632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr10:126727601 T>A maps to NM_001083914.1 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr10:126727601 T>A maps to NM_001083914.1 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr14:20388929 G>T maps to NM_001005483.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr14:20388929 G>T maps to NM_001005483.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr15:69328194 G>A maps to NM_024505.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr15:69328194 G>A maps to NM_024505.3 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr17:51900576 G>T maps to NM_032559.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr17:51900576 G>T maps to NM_032559.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr2:26647183 C>T maps to NM_145038.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr2:26647183 C>T maps to NM_145038.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr2:158165185 A>G maps to NM_014568.1 R876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr2:158165185 A>G maps to NM_014568.1 R876R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr2:219294358 C>T maps to NM_007127.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr2:219294358 C>T maps to NM_007127.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr4:189018254 G>A maps to ENST00000326754 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr4:189018254 G>A maps to ENST00000326754 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr5:169535161 C>A maps to NM_012188.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr5:169535161 C>A maps to NM_012188.4 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr7:20782598 C>T maps to NM_001163941.1 R1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr7:20782598 C>T maps to NM_001163941.1 R1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr8:77768254 C>G maps to NM_024721.4 S3033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr8:77768254 C>G maps to NM_024721.4 S3033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr9:90501882 C>G maps to NM_178828.4 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chr9:90501882 C>G maps to NM_178828.4 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:44703623 C>T maps to NM_022076.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:44703623 C>T maps to NM_022076.3 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:65819403 C>T maps to ENST00000450752 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:65819403 C>T maps to ENST00000450752 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:91873722 C>A maps to NM_032968.3 V1276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:91873722 C>A maps to NM_032968.3 V1276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:100075434 G>T maps to ENST00000415585 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:100075434 G>T maps to ENST00000415585 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:111020071 G>A maps to NM_012471.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:111020071 G>A maps to NM_012471.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:148059891 C>T maps to NM_002025.3 C1159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:148059891 C>T maps to NM_002025.3 C1159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:149931075 C>A maps to NM_003828.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4935-01A-01D-1486-08 chrX:149931075 C>A maps to NM_003828.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr1:147230395 A>G maps to NM_005266.5 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr1:147230395 A>G maps to NM_005266.5 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr11:4825511 C>T maps to ENST00000380382 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr11:4825511 C>T maps to ENST00000380382 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr11:70181754 G>A maps to NM_003626.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr11:70181754 G>A maps to NM_003626.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr12:132491423 T>C did not map to a codon.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr12:132491423 T>C did not map to a codon.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr14:88651962 G>A maps to NM_138318.2 H516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr14:88651962 G>A maps to NM_138318.2 H516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr15:43544993 G>A maps to NM_201631.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr15:43544993 G>A maps to NM_201631.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr15:90610584 C>T maps to NM_198526.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr15:90610584 C>T maps to NM_198526.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr16:9858637 A>T maps to NM_000833.3 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr16:9858637 A>T maps to NM_000833.3 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr17:17910457 C>T maps to NM_031294.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr17:17910457 C>T maps to NM_031294.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr19:362355 C>T maps to NM_016585.3 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr19:362355 C>T maps to NM_016585.3 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr20:43926657 G>A maps to ENST00000372754 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr20:43926657 G>A maps to ENST00000372754 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr3:42167077 G>A maps to NM_001042646.1 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr3:42167077 G>A maps to NM_001042646.1 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr3:97852414 C>T maps to NM_001005338.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr3:97852414 C>T maps to NM_001005338.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr3:184910534 G>A maps to NM_001966.3 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr3:184910534 G>A maps to NM_001966.3 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr6:31696722 T>C maps to NM_013974.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr6:31696722 T>C maps to NM_013974.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr6:161007523 G>T maps to NM_005577.2 P1362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr6:161007523 G>T maps to NM_005577.2 P1362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr7:98547125 G>A maps to ENST00000359863 G1618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr7:98547125 G>A maps to ENST00000359863 G1618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr9:122000990 A>G maps to NM_014618.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6191-01A-12D-1696-08 chr9:122000990 A>G maps to NM_014618.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr1:197060161 G>A maps to NM_018136.4 R3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr1:197060161 G>A maps to NM_018136.4 R3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr10:89720649 G>A did not map to a codon.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr10:89720649 G>A did not map to a codon.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr11:5906307 A>T maps to NM_001005165.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr11:5906307 A>T maps to NM_001005165.1 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr11:13441119 T>C maps to NM_032320.5 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr11:13441119 T>C maps to NM_032320.5 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr12:3121376 C>T maps to NM_003213.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr12:3121376 C>T maps to NM_003213.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr13:26343354 C>T maps to NM_016529.4 Y852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr13:26343354 C>T maps to NM_016529.4 Y852Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr15:48053910 A>G maps to NM_153618.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr15:48053910 A>G maps to NM_153618.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr2:179365814 A>T maps to NM_019091.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr2:179365814 A>T maps to NM_019091.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr2:201303920 A>C maps to ENST00000409151 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr2:201303920 A>C maps to ENST00000409151 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr22:38211152 G>A maps to NM_001171690.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr22:38211152 G>A maps to NM_001171690.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr3:140275467 G>A maps to NM_022131.2 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr3:140275467 G>A maps to NM_022131.2 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr3:141163944 C>T maps to NM_001080412.2 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr3:141163944 C>T maps to NM_001080412.2 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr3:141499457 G>A maps to NM_139209.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr3:141499457 G>A maps to NM_139209.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr4:74477539 G>T maps to NM_201431.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr4:74477539 G>T maps to NM_201431.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr4:109667591 T>C maps to NM_031279.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr4:109667591 T>C maps to NM_031279.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr5:77477402 C>T maps to NM_003664.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr5:77477402 C>T maps to NM_003664.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr5:98128832 A>G maps to NM_001012761.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr5:98128832 A>G maps to NM_001012761.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr5:169028401 G>A maps to NM_017785.4 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr5:169028401 G>A maps to NM_017785.4 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr6:28297412 C>T maps to NM_030899.4 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr6:28297412 C>T maps to NM_030899.4 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr6:35980126 G>A maps to NM_052961.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr6:35980126 G>A maps to NM_052961.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr7:47336761 G>A maps to NM_022748.11 D1198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr7:47336761 G>A maps to NM_022748.11 D1198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr7:82764221 G>A maps to NM_033026.5 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr7:82764221 G>A maps to NM_033026.5 R882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr9:75445372 C>T maps to NM_138691.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6192-01A-11D-1696-08 chr9:75445372 C>T maps to NM_138691.2 A712A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:8395552 C>T maps to ENST00000377479 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:8395552 C>T maps to ENST00000377479 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:155254427 C>G maps to NM_020897.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:155254427 C>G maps to NM_020897.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:158300835 G>A maps to NM_001764.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:158300835 G>A maps to NM_001764.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:159827988 G>C maps to NM_001013661.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr1:159827988 G>C maps to NM_001013661.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr10:15590501 G>A maps to NM_003638.1 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr10:15590501 G>A maps to NM_003638.1 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr11:55606592 T>A maps to NM_001005496.1 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr11:55606592 T>A maps to NM_001005496.1 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr12:85466876 G>T did not map to a codon.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr12:85466876 G>T did not map to a codon.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr13:49039378 C>T maps to NM_000321.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr13:49039378 C>T maps to NM_000321.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr13:73321200 A>G maps to ENST00000377815 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr13:73321200 A>G maps to ENST00000377815 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr17:3721585 G>A maps to NM_001114118.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr17:3721585 G>A maps to NM_001114118.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr17:7942478 C>T maps to NM_001141.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr17:7942478 C>T maps to NM_001141.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr17:65924655 A>G maps to ENST00000321892 Q2105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr17:65924655 A>G maps to ENST00000321892 Q2105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr19:49651353 C>T maps to NM_003660.2 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr19:49651353 C>T maps to NM_003660.2 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr3:40499406 C>T maps to NM_001034996.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr3:40499406 C>T maps to NM_001034996.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr4:80246553 G>A maps to NM_032693.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr4:80246553 G>A maps to NM_032693.2 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr4:125591833 A>G maps to NM_020337.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr4:125591833 A>G maps to NM_020337.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr5:115177233 G>A maps to ENST00000274459 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr5:115177233 G>A maps to ENST00000274459 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr5:140573540 C>T maps to NM_018930.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr5:140573540 C>T maps to NM_018930.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr7:131982915 G>T maps to NM_020911.1 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr7:131982915 G>T maps to NM_020911.1 G479G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-76-6193-01A-11D-1696-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr9:13162793 T>C maps to ENST00000319217 K1085K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-76-6193-01A-11D-1696-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-76-6193-01A-11D-1696-08 chr9:13162793 T>C maps to ENST00000319217 K1085K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr10:18828172 T>C maps to NM_201596.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr10:18828172 T>C maps to NM_201596.2 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr10:90707026 G>A maps to NM_001141945.1 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr10:90707026 G>A maps to NM_001141945.1 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr11:64882419 C>T maps to NM_003273.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr11:64882419 C>T maps to NM_003273.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr15:42193061 G>A maps to NM_139265.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr15:42193061 G>A maps to NM_139265.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr15:75045611 G>A did not map to a codon.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr15:75045611 G>A did not map to a codon.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr16:30783281 C>A maps to NM_014771.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr16:30783281 C>A maps to NM_014771.2 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr16:58079115 C>T maps to NM_002428.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr16:58079115 C>T maps to NM_002428.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr16:84449184 C>A maps to ENST00000416219 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr16:84449184 C>A maps to ENST00000416219 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:16323551 G>A maps to NM_016113.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:16323551 G>A maps to NM_016113.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:21201791 G>A did not map to a codon.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:21201791 G>A did not map to a codon.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:44067272 G>A maps to NM_001123066.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:44067272 G>A maps to NM_001123066.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:79991353 C>T maps to NM_005052.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr17:79991353 C>T maps to NM_005052.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr18:77893796 C>G maps to NM_014913.3 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr18:77893796 C>G maps to NM_014913.3 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr19:17384817 C>T maps to NM_014173.2 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr19:17384817 C>T maps to NM_014173.2 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr19:19656131 C>G maps to NM_153221.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr19:19656131 C>G maps to NM_153221.2 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr19:54800077 G>A maps to ENST00000251375 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr19:54800077 G>A maps to ENST00000251375 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr6:51491839 G>A maps to NM_138694.3 R3914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr6:51491839 G>A maps to NM_138694.3 R3914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr6:117589650 C>T maps to NM_182645.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr6:117589650 C>T maps to NM_182645.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr7:107880545 C>A did not map to a codon.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr7:107880545 C>A did not map to a codon.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr7:126173899 C>T maps to NM_001127323.1 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6280-01A-21D-1845-08 chr7:126173899 C>T maps to NM_001127323.1 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr1:170964597 C>T maps to NM_001163629.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr1:170964597 C>T maps to NM_001163629.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr15:41193043 G>A maps to NM_020857.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr15:41193043 G>A maps to NM_020857.2 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr16:830268 G>A maps to NM_001025190.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr16:830268 G>A maps to NM_001025190.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr16:2812976 C>T maps to NM_016333.3 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr16:2812976 C>T maps to NM_016333.3 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr19:9049296 C>T maps to NM_024690.2 S10778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr19:9049296 C>T maps to NM_024690.2 S10778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr2:236659062 C>T maps to NM_001037131.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr2:236659062 C>T maps to NM_001037131.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr20:39794467 T>C did not map to a codon.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr20:39794467 T>C did not map to a codon.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr22:24034584 G>A maps to ENST00000382833 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr22:24034584 G>A maps to ENST00000382833 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr22:26423541 G>A maps to ENST00000407587 A2536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr22:26423541 G>A maps to ENST00000407587 A2536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr3:14862053 T>C maps to NM_152536.3 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr3:14862053 T>C maps to NM_152536.3 Y492Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr4:55956220 G>A maps to NM_002253.2 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr4:55956220 G>A maps to NM_002253.2 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr6:16130885 C>T maps to NM_013262.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr6:16130885 C>T maps to NM_013262.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr7:97483889 A>G did not map to a codon.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr7:97483889 A>G did not map to a codon.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr8:88886130 G>C maps to NM_152418.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr8:88886130 G>C maps to NM_152418.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr8:105001596 C>T maps to NM_001100117.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6282-01A-11D-1696-08 chr8:105001596 C>T maps to NM_001100117.2 R998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:16342134 T>C maps to ENST00000375714 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:16342134 T>C maps to ENST00000375714 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:22927420 C>T maps to NM_020526.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:22927420 C>T maps to NM_020526.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:28818257 C>T maps to NM_023923.3 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:28818257 C>T maps to NM_023923.3 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:68152266 G>T maps to NM_001924.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:68152266 G>T maps to NM_001924.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:94522270 G>A maps to NM_000350.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:94522270 G>A maps to NM_000350.2 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:151491405 C>T maps to NM_020770.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:151491405 C>T maps to NM_020770.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:186134267 C>T maps to NM_031935.2 S5094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr1:186134267 C>T maps to NM_031935.2 S5094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr10:46999113 T>G maps to NM_014696.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr10:46999113 T>G maps to NM_014696.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr12:48465463 C>T maps to ENST00000004980 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr12:48465463 C>T maps to ENST00000004980 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr12:56336025 C>T maps to NM_201554.1 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr12:56336025 C>T maps to NM_201554.1 R469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr13:73372126 T>A maps to NM_006346.2 L212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr13:73372126 T>A maps to NM_006346.2 L212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr14:76107378 C>T maps to NM_017791.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr14:76107378 C>T maps to NM_017791.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr15:53081862 C>T maps to NM_004498.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr15:53081862 C>T maps to NM_004498.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr15:91184402 C>T maps to NM_022769.3 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr15:91184402 C>T maps to NM_022769.3 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr16:711896 C>T maps to NM_145294.4 R1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr16:711896 C>T maps to NM_145294.4 R1291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr18:21441698 G>A maps to ENST00000416669 A1506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr18:21441698 G>A maps to ENST00000416669 A1506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr19:6828670 C>T maps to NM_005428.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr19:6828670 C>T maps to NM_005428.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr19:46627408 A>T maps to NM_207393.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr19:46627408 A>T maps to NM_207393.1 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr19:53854578 T>C maps to NM_138374.1 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr19:53854578 T>C maps to NM_138374.1 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr2:9628295 A>G maps to NM_001039613.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr2:9628295 A>G maps to NM_001039613.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr20:56137156 G>A maps to NM_002591.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr20:56137156 G>A maps to NM_002591.3 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr20:58467200 C>T maps to NM_014258.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr20:58467200 C>T maps to NM_014258.2 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr21:31692020 G>A maps to NM_203405.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr21:31692020 G>A maps to NM_203405.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr3:52422838 G>A maps to ENST00000273600 S3191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr3:52422838 G>A maps to ENST00000273600 S3191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr4:104065618 G>A maps to NM_001813.2 Q1672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr4:104065618 G>A maps to NM_001813.2 Q1672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr4:123184109 T>C maps to NM_015312.3 A2318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr4:123184109 T>C maps to NM_015312.3 A2318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr4:147227116 C>T maps to ENST00000507030 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr4:147227116 C>T maps to ENST00000507030 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr5:122893188 G>T maps to NM_001044723.1 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr5:122893188 G>T maps to NM_001044723.1 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr5:172585745 G>A did not map to a codon.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr5:172585745 G>A did not map to a codon.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr6:32798067 A>G maps to ENST00000452392 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr6:32798067 A>G maps to ENST00000452392 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr6:43417750 C>T maps to NM_033450.2 R1439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr6:43417750 C>T maps to NM_033450.2 R1439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr8:88886277 C>T did not map to a codon.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chr8:88886277 C>T did not map to a codon.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:8555861 G>A maps to NM_000216.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:8555861 G>A maps to NM_000216.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:18238989 G>A did not map to a codon.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:18238989 G>A did not map to a codon.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:79282235 C>A maps to NM_016954.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:79282235 C>A maps to NM_016954.2 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:108924258 G>T maps to NM_022977.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6283-01A-11D-1845-08 chrX:108924258 G>T maps to NM_022977.2 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:34123558 C>T maps to ENST00000373381 P1438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:34123558 C>T maps to ENST00000373381 P1438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:57341828 C>T maps to NM_000562.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:57341828 C>T maps to NM_000562.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:152275684 C>A maps to NM_002016.1 E3893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:152275684 C>A maps to NM_002016.1 E3893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:158153825 G>A did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:158153825 G>A did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:249106331 C>A maps to NM_030645.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr1:249106331 C>A maps to NM_030645.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr10:100249841 G>A maps to NM_021828.4 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr10:100249841 G>A maps to NM_021828.4 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:18658396 T>C did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:18658396 T>C did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:52841111 A>G maps to NM_005555.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:52841111 A>G maps to NM_005555.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:57389617 G>T maps to NM_007264.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:57389617 G>T maps to NM_007264.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:117710327 G>A maps to ENST00000338101 Y567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr12:117710327 G>A maps to ENST00000338101 Y567Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr14:89130846 C>T maps to ENST00000380664 W1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr14:89130846 C>T maps to ENST00000380664 W1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr16:30409830 G>C maps to ENST00000495929 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr16:30409830 G>C maps to ENST00000495929 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr17:3524529 C>T did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr17:3524529 C>T did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr18:47463737 A>G maps to NM_001080467.2 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr18:47463737 A>G maps to NM_001080467.2 D594D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr2:174820234 A>G maps to NM_003111.4 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr2:174820234 A>G maps to NM_003111.4 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr2:207041265 G>A maps to NM_005279.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr2:207041265 G>A maps to NM_005279.3 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr20:20033097 C>T maps to NM_016652.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr20:20033097 C>T maps to NM_016652.4 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr20:23065128 G>A maps to NM_012072.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr20:23065128 G>A maps to NM_012072.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:33238054 A>C maps to NM_022553.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:33238054 A>C maps to NM_022553.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:85446873 C>T maps to NM_001080508.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:85446873 C>T maps to NM_001080508.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:125541242 G>A maps to NM_003287.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:125541242 G>A maps to NM_003287.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:158454501 C>T maps to NM_003898.3 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:158454501 C>T maps to NM_003898.3 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:161587288 C>T maps to NM_020133.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr6:161587288 C>T maps to NM_020133.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr7:66532360 G>A maps to NM_018264.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr7:66532360 G>A maps to NM_018264.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr7:103341382 C>T maps to ENST00000428762 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr7:103341382 C>T maps to ENST00000428762 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr8:143558905 C>T maps to NM_001702.2 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr8:143558905 C>T maps to NM_001702.2 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr9:132394974 G>A did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chr9:132394974 G>A did not map to a codon.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chrX:84562213 G>A maps to ENST00000373145 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6285-01A-11D-1696-08 chrX:84562213 G>A maps to ENST00000373145 Y373Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr1:150437159 T>A maps to NM_015203.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr1:150437159 T>A maps to NM_015203.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr1:237791218 C>T maps to NM_001035.2 D2093D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr1:237791218 C>T maps to NM_001035.2 D2093D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:1273708 G>A maps to ENST00000447027 S5003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:1273708 G>A maps to ENST00000447027 S5003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:7818410 G>A maps to NM_153444.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:7818410 G>A maps to NM_153444.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:65375156 C>T maps to NM_002419.3 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:65375156 C>T maps to NM_002419.3 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:93808409 C>T maps to NM_001098672.1 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr11:93808409 C>T maps to NM_001098672.1 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr12:52699174 G>A maps to NM_002284.3 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr12:52699174 G>A maps to NM_002284.3 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr12:70990027 A>G maps to NM_001109754.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr12:70990027 A>G maps to NM_001109754.1 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr13:48941693 T>G maps to NM_000321.2 L335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr13:48941693 T>G maps to NM_000321.2 L335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr14:102467293 C>T maps to NM_001376.4 R1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr14:102467293 C>T maps to NM_001376.4 R1360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr15:42193061 G>A maps to NM_139265.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr15:42193061 G>A maps to NM_139265.3 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:708350 G>A maps to NM_022463.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:708350 G>A maps to NM_022463.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:59946708 G>A maps to NM_020748.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:59946708 G>A maps to NM_020748.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:73258938 C>T maps to NM_015971.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:73258938 C>T maps to NM_015971.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr2:47206004 A>G maps to ENST00000394850 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr2:47206004 A>G maps to ENST00000394850 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr2:131984442 A>G maps to NM_001083538.1 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr2:131984442 A>G maps to NM_001083538.1 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr21:31768676 C>T maps to NM_181599.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr21:31768676 C>T maps to NM_181599.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr21:42720527 C>T maps to ENST00000398652 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr21:42720527 C>T maps to ENST00000398652 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr3:48520626 C>T maps to NM_016479.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr3:48520626 C>T maps to NM_016479.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr3:50513587 G>A maps to ENST00000435965 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr3:50513587 G>A maps to ENST00000435965 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr4:74719596 C>T maps to NM_002620.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr4:74719596 C>T maps to NM_002620.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr4:183651466 C>T maps to NM_001080477.1 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr4:183651466 C>T maps to NM_001080477.1 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr8:22972206 G>A maps to ENST00000356864 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr8:22972206 G>A maps to ENST00000356864 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr8:70617354 A>G maps to NM_030958.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr8:70617354 A>G maps to NM_030958.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr9:37515998 G>T maps to NM_012166.2 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr9:37515998 G>T maps to NM_012166.2 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr9:119770487 A>G maps to ENST00000313400 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr9:119770487 A>G maps to ENST00000313400 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr9:139250803 G>A maps to NM_001145638.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr9:139250803 G>A maps to NM_001145638.1 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chrX:147924921 C>A maps to NM_002025.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chrX:147924921 C>A maps to NM_002025.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:20944979 G>A maps to NM_001785.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:20944979 G>A maps to NM_001785.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:37356674 G>A maps to NM_000831.3 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:37356674 G>A maps to NM_000831.3 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:44086250 G>A did not map to a codon.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:44086250 G>A did not map to a codon.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:91740327 C>T maps to NM_001017975.3 E1209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:91740327 C>T maps to NM_001017975.3 E1209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:109167308 T>C maps to NM_001010883.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:109167308 T>C maps to NM_001010883.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:156713957 C>T maps to NM_001126050.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:156713957 C>T maps to NM_001126050.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:186645641 C>T maps to NM_000963.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr1:186645641 C>T maps to NM_000963.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr11:4944753 G>A maps to NM_001005237.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr11:4944753 G>A maps to NM_001005237.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr13:72147082 T>C maps to ENST00000359684 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr13:72147082 T>C maps to ENST00000359684 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr14:64450573 A>G maps to NM_182914.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr14:64450573 A>G maps to NM_182914.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr15:26026297 G>A maps to NM_024490.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr15:26026297 G>A maps to NM_024490.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr16:14029048 G>A maps to NM_005236.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr16:14029048 G>A maps to NM_005236.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr16:58587730 C>T maps to NM_016284.3 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr16:58587730 C>T maps to NM_016284.3 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr17:10215248 G>A maps to NM_003802.2 R1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr17:10215248 G>A maps to NM_003802.2 R1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:3918803 C>T maps to NM_033064.4 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:3918803 C>T maps to NM_033064.4 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:6669942 C>T maps to NM_003807.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:6669942 C>T maps to NM_003807.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:9082858 T>A maps to NM_024690.2 R2986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:9082858 T>A maps to NM_024690.2 R2986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:15289675 C>T maps to NM_000435.2 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:15289675 C>T maps to NM_000435.2 P1265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:18180413 G>A maps to NM_005535.1 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr19:18180413 G>A maps to NM_005535.1 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr2:207509343 G>A maps to NM_001102659.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr2:207509343 G>A maps to NM_001102659.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr20:61595025 C>T maps to NM_022082.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr20:61595025 C>T maps to NM_022082.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr21:45919791 C>T maps to ENST00000443468 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr21:45919791 C>T maps to ENST00000443468 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr22:22843648 G>A maps to NM_080764.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr22:22843648 G>A maps to NM_080764.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr22:43603578 C>T maps to NM_173050.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr22:43603578 C>T maps to NM_173050.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr4:159052125 T>C maps to NM_001128424.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr4:159052125 T>C maps to NM_001128424.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr5:428028 C>T maps to NM_020731.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr5:428028 C>T maps to NM_020731.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr5:101599410 G>A maps to NM_180991.4 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr5:101599410 G>A maps to NM_180991.4 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr5:140554074 C>T maps to NM_018940.2 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr5:140554074 C>T maps to NM_018940.2 D553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr6:101073205 A>G maps to NM_006828.2 I1549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr6:101073205 A>G maps to NM_006828.2 I1549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:4189056 G>A maps to NM_152744.3 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:4189056 G>A maps to NM_152744.3 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:30830977 C>T maps to NM_032222.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:30830977 C>T maps to NM_032222.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:71571178 G>A maps to NM_031468.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:119915030 C>T maps to NM_012281.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:119915030 C>T maps to NM_012281.2 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:128445463 G>A maps to NM_022742.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr7:128445463 G>A maps to NM_022742.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr9:137716531 C>T maps to NM_000093.3 D1595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6656-01A-11D-1845-08 chr9:137716531 C>T maps to NM_000093.3 D1595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:6209437 C>T maps to NM_015557.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:6209437 C>T maps to NM_015557.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:110293380 G>A maps to NM_139053.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:110293380 G>A maps to NM_139053.1 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:158549257 G>A maps to NM_001004477.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:158549257 G>A maps to NM_001004477.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:173010833 C>T maps to NM_005092.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:173010833 C>T maps to NM_005092.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:178427054 A>T maps to ENST00000263528 G865G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:178427054 A>T maps to ENST00000263528 G865G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:248636974 C>T maps to NM_001005495.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr1:248636974 C>T maps to NM_001005495.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr11:104899922 C>A maps to NM_033292.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr11:104899922 C>A maps to NM_033292.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr12:85695205 C>T maps to NM_006982.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr12:85695205 C>T maps to NM_006982.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr14:105622279 C>T maps to NM_002226.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr14:105622279 C>T maps to NM_002226.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr15:85383055 C>T maps to NM_020778.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr15:85383055 C>T maps to NM_020778.4 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr15:91341565 G>A maps to NM_000057.2 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr15:91341565 G>A maps to NM_000057.2 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr16:20494408 G>A maps to NM_001010845.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr16:20494408 G>A maps to NM_001010845.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr17:29556483 G>A did not map to a codon.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr17:29556483 G>A did not map to a codon.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr2:170677784 T>C did not map to a codon.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr2:170677784 T>C did not map to a codon.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr20:50407509 G>A maps to NM_020436.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr20:50407509 G>A maps to NM_020436.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr5:13885212 G>A maps to NM_001369.2 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr5:13885212 G>A maps to NM_001369.2 R956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr6:154831212 C>T maps to NM_173515.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr6:154831212 C>T maps to NM_173515.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr7:56144569 C>T maps to ENST00000395437 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr7:56144569 C>T maps to ENST00000395437 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr8:104388027 C>T maps to NM_138455.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6657-01A-11D-1845-08 chr8:104388027 C>T maps to NM_138455.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr1:246078866 C>A maps to NM_001167740.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr1:246078866 C>A maps to NM_001167740.1 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr10:124395539 A>G maps to ENST00000368915 E2194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr10:124395539 A>G maps to ENST00000368915 E2194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr11:7083704 A>G maps to NM_176822.3 R982R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr11:7083704 A>G maps to NM_176822.3 R982R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr11:32421504 T>G maps to NM_024426.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr11:32421504 T>G maps to NM_024426.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr11:63961717 C>T maps to ENST00000358794 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr11:63961717 C>T maps to ENST00000358794 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr13:36686059 G>A maps to NM_004734.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr13:36686059 G>A maps to NM_004734.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr14:32560333 G>A maps to NM_001030055.1 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr14:32560333 G>A maps to NM_001030055.1 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr14:52735335 G>A maps to NM_000953.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr14:52735335 G>A maps to NM_000953.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr15:50226280 G>T maps to NM_024837.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr15:50226280 G>T maps to NM_024837.2 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr17:56492698 T>C maps to NM_017763.4 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr17:56492698 T>C maps to NM_017763.4 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr19:10886490 G>A maps to NM_001005361.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr19:10886490 G>A maps to NM_001005361.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr2:74900662 G>A maps to NM_004263.3 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr2:74900662 G>A maps to NM_004263.3 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr2:125530547 G>A maps to NM_130773.2 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr2:125530547 G>A maps to NM_130773.2 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr2:230683175 T>C maps to ENST00000389044 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr2:230683175 T>C maps to ENST00000389044 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr20:19981288 C>T maps to ENST00000255006 N848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr20:19981288 C>T maps to ENST00000255006 N848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr21:40883644 C>T maps to NM_007341.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr21:40883644 C>T maps to NM_007341.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr3:78683175 G>A maps to NM_002941.3 D1130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr3:78683175 G>A maps to NM_002941.3 D1130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr3:132432100 G>A maps to ENST00000393156 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr3:132432100 G>A maps to ENST00000393156 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr3:197431551 G>A maps to NM_014687.1 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr3:197431551 G>A maps to NM_014687.1 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr4:20597370 C>T maps to ENST00000273739 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr4:20597370 C>T maps to ENST00000273739 D1091D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr4:169845563 C>T maps to NM_001166108.1 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr4:169845563 C>T maps to NM_001166108.1 R1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr5:161300156 G>A maps to NM_001127648.1 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr5:161300156 G>A maps to NM_001127648.1 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr5:177547669 C>T maps to NM_015111.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr5:177547669 C>T maps to NM_015111.1 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr6:80838914 T>C maps to NM_183050.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr6:80838914 T>C maps to NM_183050.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr6:135748440 T>C maps to NM_017651.4 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr6:135748440 T>C maps to NM_017651.4 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr7:55912358 G>A maps to NM_207366.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr7:55912358 G>A maps to NM_207366.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr7:107415298 G>A maps to NM_000111.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr7:107415298 G>A maps to NM_000111.2 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr8:142367057 G>A maps to NM_005293.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr8:142367057 G>A maps to NM_005293.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr9:74319625 G>A maps to NM_013390.2 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr9:74319625 G>A maps to NM_013390.2 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr9:131482498 G>A maps to NM_013355.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr9:131482498 G>A maps to NM_013355.3 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr9:138662161 G>A maps to ENST00000298480 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chr9:138662161 G>A maps to ENST00000298480 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chrX:130409144 C>T maps to NM_001170961.1 K1105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chrX:130409144 C>T maps to NM_001170961.1 K1105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chrX:140995943 T>C maps to NM_005462.4 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6660-01A-11D-1845-08 chrX:140995943 T>C maps to NM_005462.4 F918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr1:169698647 G>A maps to NM_000450.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr1:169698647 G>A maps to NM_000450.2 N294N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr11:59211186 C>T maps to NM_001004728.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr11:59211186 C>T maps to NM_001004728.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr12:402171 A>C maps to NM_001042603.1 L1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr12:402171 A>C maps to NM_001042603.1 L1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr16:81942085 G>A maps to NM_002661.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr16:81942085 G>A maps to NM_002661.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr18:28671014 A>C maps to ENST00000438199 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr18:28671014 A>C maps to ENST00000438199 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr19:4171162 C>T maps to NM_032607.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr19:4171162 C>T maps to NM_032607.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr19:8616650 G>A maps to NM_012335.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr19:8616650 G>A maps to NM_012335.3 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr20:43118146 C>T maps to NM_024331.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr20:43118146 C>T maps to NM_024331.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr3:182871532 G>A maps to NM_014398.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr3:182871532 G>A maps to NM_014398.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr3:184295701 G>A maps to NM_004443.3 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr3:184295701 G>A maps to NM_004443.3 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr3:184870497 G>A maps to NM_001025266.1 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr3:184870497 G>A maps to NM_001025266.1 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr4:39462477 C>A maps to NM_006859.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr4:39462477 C>A maps to NM_006859.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr5:127674666 C>A maps to NM_001999.3 E1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr5:127674666 C>A maps to NM_001999.3 E1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr5:128862026 C>T maps to NM_133638.3 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr5:128862026 C>T maps to NM_133638.3 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr5:140203027 C>T maps to NM_018908.2 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr5:140203027 C>T maps to NM_018908.2 D556D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr6:142409495 G>A maps to NM_002511.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr6:142409495 G>A maps to NM_002511.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr7:43351507 C>T maps to NM_015052.3 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr7:43351507 C>T maps to NM_015052.3 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr7:117067469 G>A maps to NM_130768.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr7:117067469 G>A maps to NM_130768.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr7:150934491 C>G maps to NM_019015.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr7:150934491 C>G maps to NM_019015.1 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr8:10469500 G>A maps to NM_178857.5 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr8:10469500 G>A maps to NM_178857.5 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr9:130689472 G>A maps to NM_001135219.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6661-01B-11D-1845-08 chr9:130689472 G>A maps to NM_001135219.1 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr1:248224732 C>A maps to NM_001004687.1 Y250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr1:248224732 C>A maps to NM_001004687.1 Y250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr10:122649466 T>C maps to NM_018117.11 N763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr10:122649466 T>C maps to NM_018117.11 N763N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr11:95825766 C>T maps to NM_032427.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr11:95825766 C>T maps to NM_032427.1 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr15:40590477 G>A maps to NM_004573.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr15:40590477 G>A maps to NM_004573.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr17:47297533 C>T maps to NM_016428.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr17:47297533 C>T maps to NM_016428.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr17:76459048 G>A maps to ENST00000389840 P3003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr17:76459048 G>A maps to ENST00000389840 P3003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr17:80858559 G>A maps to NM_005993.4 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr17:80858559 G>A maps to NM_005993.4 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr2:179485026 G>A maps to NM_133378.4 D12839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr2:179485026 G>A maps to NM_133378.4 D12839D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr4:183714568 T>C maps to NM_001080477.1 F2248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr4:183714568 T>C maps to NM_001080477.1 F2248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr6:168443280 G>A maps to NM_030615.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr6:168443280 G>A maps to NM_030615.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr9:137309041 G>T maps to NM_002957.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6662-01A-11D-1845-08 chr9:137309041 G>T maps to NM_002957.4 E217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr1:86952276 G>A maps to NM_001285.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr1:86952276 G>A maps to NM_001285.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr10:135020648 C>A maps to ENST00000368572 Y1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr10:135020648 C>A maps to ENST00000368572 Y1198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr11:18955701 C>T maps to NM_147199.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr11:18955701 C>T maps to NM_147199.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr12:18435194 A>G maps to NM_004570.4 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr12:18435194 A>G maps to NM_004570.4 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr12:100433499 G>A maps to NM_015054.1 T1383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr12:100433499 G>A maps to NM_015054.1 T1383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr13:49039398 C>A maps to NM_000321.2 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr13:49039398 C>A maps to NM_000321.2 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr17:29497002 C>T maps to NM_001042492.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr17:29497002 C>T maps to NM_001042492.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr17:34432023 G>A maps to NM_002984.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr17:34432023 G>A maps to NM_002984.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr17:61995750 G>A maps to NM_000515.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr17:61995750 G>A maps to NM_000515.3 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr18:7009320 C>T maps to NM_005559.2 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr18:7009320 C>T maps to NM_005559.2 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr19:31039822 C>T maps to NM_014717.1 H1099H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr19:31039822 C>T maps to NM_014717.1 H1099H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr2:179497280 C>T maps to NM_133378.4 K11916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr2:179497280 C>T maps to NM_133378.4 K11916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr20:43034797 C>T maps to ENST00000338692 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr20:43034797 C>T maps to ENST00000338692 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr5:45262328 C>T maps to NM_021072.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr5:45262328 C>T maps to NM_021072.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr5:89986755 C>T maps to NM_032119.3 G2283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr5:89986755 C>T maps to NM_032119.3 G2283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr6:37438826 G>A maps to NM_015050.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr6:37438826 G>A maps to NM_015050.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr7:1538053 C>T maps to ENST00000389470 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr7:1538053 C>T maps to ENST00000389470 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:16435989 G>A maps to NM_017637.5 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:16435989 G>A maps to NM_017637.5 G734G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:27948962 C>A maps to NM_152570.1 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:27948962 C>A maps to NM_152570.1 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:96408030 G>A maps to NM_005392.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:96408030 G>A maps to NM_005392.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:107331657 C>T maps to NM_001004483.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chr9:107331657 C>T maps to NM_001004483.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chrX:107160961 G>A maps to NM_012216.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6663-01A-11D-1845-08 chrX:107160961 G>A maps to NM_012216.3 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr10:89692767 A>C did not map to a codon.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr10:89692767 A>C did not map to a codon.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr11:82443598 C>T maps to NM_175885.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr11:82443598 C>T maps to NM_175885.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr11:89073228 A>T did not map to a codon.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr11:89073228 A>T did not map to a codon.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr13:33685934 C>A maps to NM_178007.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr13:33685934 C>A maps to NM_178007.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr13:99337142 C>T maps to NM_005073.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr13:99337142 C>T maps to NM_005073.3 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr15:39879563 C>T maps to NM_003246.2 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr15:39879563 C>T maps to NM_003246.2 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr16:315017 G>A maps to NM_032039.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr16:315017 G>A maps to NM_032039.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr17:7139422 G>A maps to NM_024297.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr17:7139422 G>A maps to NM_024297.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr19:6495600 G>A maps to NM_006087.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr19:6495600 G>A maps to NM_006087.2 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr19:9089510 G>A maps to NM_024690.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr19:9089510 G>A maps to NM_024690.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr19:14071179 G>C maps to NM_138353.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr19:14071179 G>C maps to NM_138353.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr2:26950538 C>T maps to NM_002246.2 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr2:26950538 C>T maps to NM_002246.2 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr20:21367620 C>A maps to NM_012255.3 R922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr20:21367620 C>A maps to NM_012255.3 R922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr20:44639884 C>T maps to NM_004994.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr20:44639884 C>T maps to NM_004994.2 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr5:178555035 G>A maps to NM_014244.4 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr5:178555035 G>A maps to NM_014244.4 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr6:160240042 G>A maps to NM_173516.1 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr6:160240042 G>A maps to NM_173516.1 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr7:18066637 T>A maps to NM_175886.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr7:18066637 T>A maps to NM_175886.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr8:87666238 C>T did not map to a codon.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr8:87666238 C>T did not map to a codon.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr9:990869 C>T maps to NM_021240.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chr9:990869 C>T maps to NM_021240.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chrX:7870100 G>A maps to NM_001142389.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chrX:7870100 G>A maps to NM_001142389.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chrX:21995313 G>A maps to NM_004595.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chrX:21995313 G>A maps to NM_004595.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chrX:103080387 C>T maps to NM_016370.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6664-01A-11D-1845-08 chrX:103080387 C>T maps to NM_016370.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr1:79094654 C>T maps to NM_006820.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr1:79094654 C>T maps to NM_006820.2 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr12:2602398 G>A maps to NM_199460.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr12:2602398 G>A maps to NM_199460.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr13:113852563 C>T maps to ENST00000246505 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr13:113852563 C>T maps to ENST00000246505 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr15:23931737 G>A maps to NM_002487.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr15:23931737 G>A maps to NM_002487.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr16:20651782 C>T maps to NM_052956.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr16:20651782 C>T maps to NM_052956.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr16:81181774 G>A maps to NM_052892.3 D1647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr16:81181774 G>A maps to NM_052892.3 D1647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr18:6956724 G>A maps to NM_005559.2 V2668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr18:6956724 G>A maps to NM_005559.2 V2668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr18:42532157 C>T maps to NM_015559.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr18:42532157 C>T maps to NM_015559.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr19:30934789 C>T maps to NM_014717.1 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr19:30934789 C>T maps to NM_014717.1 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr19:34895690 C>T maps to NM_032346.1 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr19:34895690 C>T maps to NM_032346.1 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr19:38990275 C>T maps to NM_000540.2 G2343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr19:38990275 C>T maps to NM_000540.2 G2343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr2:168100109 C>T maps to NM_152381.5 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr2:168100109 C>T maps to NM_152381.5 F736F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr2:179498194 G>A maps to NM_133378.4 G11729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr2:179498194 G>A maps to NM_133378.4 G11729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr2:223066891 G>A maps to NM_181459.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr2:223066891 G>A maps to NM_181459.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr4:25416008 T>C did not map to a codon.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr4:25416008 T>C did not map to a codon.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr7:99691888 G>A maps to NM_005916.3 Y585Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr7:99691888 G>A maps to NM_005916.3 Y585Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr7:102669856 C>T maps to NM_145032.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr7:102669856 C>T maps to NM_145032.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr7:144098553 C>T maps to ENST00000467773 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr7:144098553 C>T maps to ENST00000467773 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr9:129854000 C>T maps to NM_012098.2 W410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chr9:129854000 C>T maps to NM_012098.2 W410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chrX:123171415 C>T maps to NM_001042750.1 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5910-01A-11D-1696-08 chrX:123171415 C>T maps to NM_001042750.1 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr11:55798502 C>T maps to NM_001001921.1 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr11:55798502 C>T maps to NM_001001921.1 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr11:61615698 G>A maps to NM_004265.2 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr11:61615698 G>A maps to NM_004265.2 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr13:48934207 T>A maps to NM_000321.2 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr13:48934207 T>A maps to NM_000321.2 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr17:62532770 C>T maps to NM_138363.1 R708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr17:62532770 C>T maps to NM_138363.1 R708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr2:102805704 C>T maps to NM_003854.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr2:102805704 C>T maps to NM_003854.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr4:79400816 C>T maps to NM_025074.6 N2796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr4:79400816 C>T maps to NM_025074.6 N2796N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr7:45216935 C>T maps to NM_005856.2 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr7:45216935 C>T maps to NM_005856.2 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr7:76112452 C>T maps to NM_020892.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-81-5911-01A-12D-1845-08 chr7:76112452 C>T maps to NM_020892.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr1:84961637 C>G maps to NM_025065.6 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr1:84961637 C>G maps to NM_025065.6 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr1:153409548 G>A maps to NM_001045479.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr1:153409548 G>A maps to NM_001045479.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr12:48371797 G>A maps to NM_001844.4 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr12:48371797 G>A maps to NM_001844.4 R1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr14:50089071 G>A maps to NM_002408.3 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr14:50089071 G>A maps to NM_002408.3 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr14:70237709 A>T did not map to a codon.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr14:70237709 A>T did not map to a codon.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr15:75980828 A>C maps to NM_001897.4 Y859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr15:75980828 A>C maps to NM_001897.4 Y859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr15:90142687 A>G maps to NM_152259.3 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr15:90142687 A>G maps to NM_152259.3 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr16:89598460 G>A maps to NM_003119.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr16:89598460 G>A maps to NM_003119.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr17:38641224 G>A maps to NM_032865.5 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr17:38641224 G>A maps to NM_032865.5 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr17:48246590 C>T maps to NM_000023.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr17:48246590 C>T maps to NM_000023.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr17:56277731 C>T maps to NM_000502.4 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr17:56277731 C>T maps to NM_000502.4 R562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr18:6977851 G>A maps to NM_005559.2 D2073D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr18:6977851 G>A maps to NM_005559.2 D2073D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr18:14542920 G>A maps to ENST00000444806 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr18:14542920 G>A maps to ENST00000444806 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr18:61387389 G>A did not map to a codon.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr18:61387389 G>A did not map to a codon.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:5273495 C>T maps to NM_002850.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:5273495 C>T maps to NM_002850.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:35979578 G>A maps to NM_207392.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:35979578 G>A maps to NM_207392.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:38621244 C>T maps to NM_015073.1 D992D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:38621244 C>T maps to NM_015073.1 D992D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:41133126 C>T maps to ENST00000308370 D1477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:41133126 C>T maps to ENST00000308370 D1477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:42301581 G>A maps to NM_001815.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:42301581 G>A maps to NM_001815.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:43383724 G>T maps to NM_006905.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr19:43383724 G>T maps to NM_006905.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr2:3392071 C>T maps to NM_016030.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr2:3392071 C>T maps to NM_016030.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr2:107460196 C>T maps to NM_001142351.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr2:107460196 C>T maps to NM_001142351.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr5:39153686 C>T maps to ENST00000263405 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr5:39153686 C>T maps to ENST00000263405 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr5:122754204 C>T maps to NM_153223.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr5:122754204 C>T maps to NM_153223.3 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr6:38957816 G>A maps to ENST00000327475 P4349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr6:38957816 G>A maps to ENST00000327475 P4349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:7612688 C>T maps to NM_019005.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:7612688 C>T maps to NM_019005.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:48450228 G>T maps to NM_152701.3 L4061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:48450228 G>T maps to NM_152701.3 L4061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:53104047 C>A maps to NM_182595.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:53104047 C>A maps to NM_182595.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:72717905 G>A maps to NM_148956.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:72717905 G>A maps to NM_148956.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:142566032 C>T maps to NM_004445.3 Y651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr7:142566032 C>T maps to NM_004445.3 Y651Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr8:67507921 G>A maps to NM_001080416.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chr8:67507921 G>A maps to NM_001080416.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chrX:20074864 C>T maps to NM_001168465.1 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chrX:20074864 C>T maps to NM_001168465.1 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chrX:57935324 G>A maps to NM_007156.4 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chrX:57935324 G>A maps to NM_007156.4 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chrX:119243158 G>A maps to NM_139282.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-87-5896-01A-01D-1696-08 chrX:119243158 G>A maps to NM_139282.1 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr9:39888188 G>T maps to ENST00000377642 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-02-2470-01A-01D-1494-08 chr9:39888188 G>T maps to ENST00000377642 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr17:29667595 C>A maps to NM_001042492.2 S2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr17:29667595 C>A maps to NM_001042492.2 S2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr8:105264035 C>A maps to NM_001100117.2 Y1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0124-01A-01D-1490-08 chr8:105264035 C>A maps to NM_001100117.2 Y1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr15:57555308 G>C did not map to a codon.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr15:57555308 G>C did not map to a codon.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr16:202973 C>T maps to NM_005332.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0128-01A-01D-1490-08 chr16:202973 C>T maps to NM_005332.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr3:49836330 C>T maps to NM_001007540.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0155-01B-01D-1492-08 chr3:49836330 C>T maps to NM_001007540.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:99145994 A>C maps to NM_145111.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0174-01A-01D-1491-08 chr7:99145994 A>C maps to NM_145111.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr4:48537845 T>C did not map to a codon.
Sequencing variant TCGA-06-0686-01A-01W-0348-08 chr4:48537845 T>C did not map to a codon.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:70308328 G>A maps to NM_004536.2 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-0743-01A-01D-1492-08 chr5:70308328 G>A maps to NM_004536.2 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr10:17949553 G>A maps to NM_002438.2 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-06-5413-01A-01D-1696-08 chr10:17949553 G>A maps to NM_002438.2 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr17:29661944 C>T maps to NM_001042492.2 R1968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-14-1043-01B-11D-1845-08 chr17:29661944 C>T maps to NM_001042492.2 R1968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr3:57493504 G>A maps to NM_178504.4 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr3:57493504 G>A maps to NM_178504.4 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr9:140173548 C>T maps to NM_017723.2 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-1979-01A-01D-1696-08 chr9:140173548 C>T maps to NM_017723.2 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr20:3640879 G>T maps to NM_145762.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-32-4719-01A-01D-1353-08 chr20:3640879 G>T maps to NM_145762.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:37924769 T>A maps to NM_016616.4 L388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-4927-01A-01D-1486-08 chr7:37924769 T>A maps to NM_016616.4 L388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:36288288 C>T maps to NM_001123391.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-76-6286-01A-11D-1845-08 chr17:36288288 C>T maps to NM_001123391.2 P125P. Only missense variants will be evaluated by CHASM.
