6479 NP_109597 V157F not found in SNVbox database
410 NP_001070868 S667L not found in SNVbox database
683 NP_001070868 K508N not found in SNVbox database
733 NP_001070868 G14R not found in SNVbox database
788 NP_001070868 L323I not found in SNVbox database
1892 NP_001070868 A760T not found in SNVbox database
1907 NP_001070868 V481A not found in SNVbox database
2333 NP_001070868 L286F not found in SNVbox database
2489 NP_001070868 P678S not found in SNVbox database
2551 NP_001070868 R525W not found in SNVbox database
3422 NP_001070868 T424A not found in SNVbox database
3686 NP_001070868 I472M not found in SNVbox database
3713 NP_001070868 R689Q not found in SNVbox database
4626 NP_001070868 G72D not found in SNVbox database
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:19549913 G>A maps to NM_015047.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:19549913 G>A maps to NM_015047.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:145534099 C>G maps to NM_003637.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:145534099 C>G maps to NM_003637.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:153362975 G>A maps to NM_002964.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:153362975 G>A maps to NM_002964.4 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:156281972 C>G maps to NM_005998.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:156281972 C>G maps to NM_005998.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:183209494 C>T maps to NM_005562.2 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr1:183209494 C>T maps to NM_005562.2 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:61607464 G>A maps to NM_014709.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:61607464 G>A maps to NM_014709.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:179616158 A>C maps to ENST00000375038 T3658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:179616158 A>C maps to ENST00000375038 T3658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:200137184 G>A maps to NM_001172509.1 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:200137184 G>A maps to NM_001172509.1 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:219290519 C>T maps to NM_007127.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr2:219290519 C>T maps to NM_007127.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:49135632 G>A maps to NM_005051.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:49135632 G>A maps to NM_005051.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:49721755 C>T maps to NM_020998.3 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:49721755 C>T maps to NM_020998.3 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:50231194 C>T maps to NM_000172.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:50231194 C>T maps to NM_000172.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:195477928 C>T maps to NM_018406.5 S5234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr3:195477928 C>T maps to NM_018406.5 S5234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:3451001 C>T maps to ENST00000511533 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:3451001 C>T maps to ENST00000511533 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:114251494 T>C maps to NM_001148.4 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:114251494 T>C maps to NM_001148.4 C998C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:164534482 G>T maps to ENST00000514618 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:164534482 G>T maps to ENST00000514618 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:185941787 G>A maps to NM_001029887.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr4:185941787 G>A maps to NM_001029887.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:13865841 A>G maps to NM_001369.2 Y1430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:13865841 A>G maps to NM_001369.2 Y1430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:66462290 G>A maps to NM_001164664.1 P2428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:66462290 G>A maps to NM_001164664.1 P2428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:121786335 T>A maps to ENST00000379533 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:121786335 T>A maps to ENST00000379533 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:131607547 G>A maps to NM_003687.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:131607547 G>A maps to NM_003687.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:134041066 C>T maps to NM_021982.1 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:134041066 C>T maps to NM_021982.1 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:145895382 C>T maps to NM_194251.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:176522355 C>A maps to NM_213647.1 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr5:176522355 C>A maps to NM_213647.1 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr6:42236136 G>A maps to NM_033502.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr6:42236136 G>A maps to NM_033502.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr6:119232919 A>G maps to ENST00000316316 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr6:119232919 A>G maps to ENST00000316316 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:2586959 G>A maps to NM_152743.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:2586959 G>A maps to NM_152743.3 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:94047864 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:94047864 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:120740099 G>T maps to NM_024913.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr7:120740099 G>T maps to NM_024913.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr8:77776626 C>T maps to NM_024721.4 C3559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr8:77776626 C>T maps to NM_024721.4 C3559C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr8:95674783 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr8:95674783 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:130928555 G>A maps to NM_012127.2 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:130928555 G>A maps to NM_012127.2 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:136211044 G>C maps to NM_133640.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:136211044 G>C maps to NM_133640.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:139702036 C>T maps to NM_001039374.4 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:139702036 C>T maps to NM_001039374.4 F500F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:140109623 G>A maps to NM_001144026.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr9:140109623 G>A maps to NM_001144026.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr11:11394085 G>A maps to NM_198516.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr11:11394085 G>A maps to NM_198516.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr11:65417471 C>A maps to NM_153253.29 S933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr11:65417471 C>A maps to NM_153253.29 S933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr12:105601772 C>A maps to NM_018171.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr12:105601772 C>A maps to NM_018171.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr12:106712242 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr12:106712242 G>A did not map to a codon.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:20041438 G>T maps to NM_199254.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:20041438 G>T maps to NM_199254.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:23929790 G>A maps to NM_014363.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:23929790 G>A maps to NM_014363.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:52971454 C>T maps to NM_018676.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr13:52971454 C>T maps to NM_018676.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:65253697 C>T maps to ENST00000389723 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:65253697 C>T maps to ENST00000389723 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:70490102 G>T maps to NM_001034852.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:70490102 G>T maps to NM_001034852.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:74194192 C>T maps to NM_001043318.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr14:74194192 C>T maps to NM_001043318.1 V710V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:34105681 G>A maps to NM_001036.3 L3468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:34105681 G>A maps to NM_001036.3 L3468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:54306222 C>T maps to ENST00000260323 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:54306222 C>T maps to ENST00000260323 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:72338070 T>C maps to ENST00000424560 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:72338070 T>C maps to ENST00000424560 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr16:1535987 G>A maps to NM_001013658.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr16:1535987 G>A maps to NM_001013658.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr16:72984604 G>A maps to NM_006885.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr16:72984604 G>A maps to NM_006885.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:10411686 C>T maps to NM_005963.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:10411686 C>T maps to NM_005963.3 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:34893432 C>G maps to NM_178517.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:34893432 C>G maps to NM_178517.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:40837382 C>T maps to NM_003632.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:40837382 C>T maps to NM_003632.2 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:58040311 G>A maps to NM_016125.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr17:58040311 G>A maps to NM_016125.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr18:33606927 G>T maps to NM_018170.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr18:33606927 G>T maps to NM_018170.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:23351020 G>C maps to NM_022482.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:23351020 G>C maps to NM_022482.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:39986943 C>T maps to NM_022896.1 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:39986943 C>T maps to NM_022896.1 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:62724216 C>T maps to NM_000913.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr20:62724216 C>T maps to NM_000913.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr21:46078006 C>T maps to NM_198697.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr21:46078006 C>T maps to NM_198697.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr22:32889254 G>A maps to NM_012179.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr22:32889254 G>A maps to NM_012179.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chrX:84363233 G>A maps to NM_001012980.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chrX:84363233 G>A maps to NM_001012980.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:32694655 A>G maps to NM_016252.3 E2107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:32694655 A>G maps to NM_016252.3 E2107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:100167950 G>A maps to NM_001025108.1 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:100167950 G>A maps to NM_001025108.1 S1247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:219884301 C>T maps to NM_194302.2 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:219884301 C>T maps to NM_194302.2 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:220337741 C>T maps to NM_005876.4 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr2:220337741 C>T maps to NM_005876.4 F1357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr3:46414641 C>T maps to NM_001100168.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr3:46414641 C>T maps to NM_001100168.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr5:75594617 G>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr5:75594617 G>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr5:101592817 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr5:101592817 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:43174207 C>T maps to ENST00000354495 F1724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:43174207 C>T maps to ENST00000354495 F1724F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:43305864 A>T maps to NM_014345.2 A1957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:43305864 A>T maps to NM_014345.2 A1957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:131979501 A>G maps to NM_005021.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:131979501 A>G maps to NM_005021.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:142725100 G>T maps to NM_198569.2 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:142725100 G>T maps to NM_198569.2 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:157517417 C>T maps to ENST00000367148 Q1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr6:157517417 C>T maps to ENST00000367148 Q1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr7:19184847 G>A maps to NM_152898.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr7:19184847 G>A maps to NM_152898.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr7:25264764 A>G maps to NM_022150.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr7:25264764 A>G maps to NM_022150.3 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr9:16437455 G>A maps to NM_017637.5 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr9:16437455 G>A maps to NM_017637.5 Q246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr10:128193174 G>A maps to NM_001004298.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr10:128193174 G>A maps to NM_001004298.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr11:67219577 G>C maps to NM_206997.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr11:67219577 G>C maps to NM_206997.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr11:132527207 G>T maps to NM_002545.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr11:132527207 G>T maps to NM_002545.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:121693607 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:121693607 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:123067478 G>C maps to NM_014708.4 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:123067478 G>C maps to NM_014708.4 L1070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:124416628 C>A maps to NM_207437.3 R4306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr12:124416628 C>A maps to NM_207437.3 R4306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr15:30938315 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:24920407 C>T maps to NM_052944.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:24920407 C>T maps to NM_052944.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:28847396 C>G maps to NM_148414.1 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:28847396 C>G maps to NM_148414.1 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:84684520 C>T maps to NM_024731.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr16:84684520 C>T maps to NM_024731.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:39967425 G>A maps to NM_006455.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:39967425 G>A maps to NM_006455.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:42937867 G>A maps to NM_004247.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:42937867 G>A maps to NM_004247.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:71398262 C>A maps to NM_001144952.1 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr17:71398262 C>A maps to NM_001144952.1 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr18:21492789 C>G maps to ENST00000416669 S2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr18:21492789 C>G maps to ENST00000416669 S2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr18:59855015 C>G maps to NM_020854.3 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr18:59855015 C>G maps to NM_020854.3 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:7810764 C>A maps to NM_021155.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:7810764 C>A maps to NM_021155.3 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:41248514 C>T maps to NM_198476.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:41248514 C>T maps to NM_198476.3 K293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:51958720 C>T maps to NM_014442.2 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:51958720 C>T maps to NM_014442.2 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:53912232 C>T maps to NM_001040185.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr19:53912232 C>T maps to NM_001040185.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr20:3007824 G>A maps to NM_002836.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chr20:3007824 G>A maps to NM_002836.3 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chrX:134166742 C>T maps to NM_001078171.1 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13I-01A-11D-A13W-08 chrX:134166742 C>T maps to NM_001078171.1 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr1:154321467 G>T maps to NM_020452.3 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr1:154321467 G>T maps to NM_020452.3 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr1:211276925 C>G maps to NM_172362.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr1:211276925 C>G maps to NM_172362.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr2:135308214 G>A maps to NM_030923.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr2:135308214 G>A maps to NM_030923.4 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr2:197650252 G>C maps to NM_012086.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr2:197650252 G>C maps to NM_012086.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:48573762 G>T maps to NM_004567.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:48573762 G>T maps to NM_004567.2 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:50684225 C>A maps to NM_004635.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:50684225 C>A maps to NM_004635.3 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:50685380 C>T maps to NM_004635.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:50685380 C>T maps to NM_004635.3 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:57827024 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr3:57827024 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:74363403 C>G maps to NM_001133.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:74363403 C>G maps to NM_001133.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:83776176 G>A maps to ENST00000505472 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:83776176 G>A maps to ENST00000505472 I629I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:100532320 G>C maps to ENST00000511045 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr4:100532320 G>C maps to ENST00000511045 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:60083197 C>T maps to NM_024930.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:60083197 C>T maps to NM_024930.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:89985849 A>T maps to NM_032119.3 A2221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:89985849 A>T maps to NM_032119.3 A2221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:140167230 G>A maps to NM_018900.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr5:140167230 G>A maps to NM_018900.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr6:105609535 T>C maps to NM_022361.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr6:105609535 T>C maps to NM_022361.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr6:166571979 C>A maps to NM_003181.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr6:166571979 C>A maps to NM_003181.2 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:126544098 T>A maps to NM_001127323.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:126544098 T>A maps to NM_001127323.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:133812299 C>A maps to NM_144648.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr7:133812299 C>A maps to NM_144648.1 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr8:6357450 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr8:6357450 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr8:36793050 A>T maps to NM_001031836.2 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr8:36793050 A>T maps to NM_001031836.2 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr9:104192126 G>A maps to NM_000035.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr9:104192126 G>A maps to NM_000035.3 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr10:29777620 G>A maps to NM_021738.2 S1419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr10:29777620 G>A maps to NM_021738.2 S1419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr10:123843280 C>T maps to NM_206862.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr10:123843280 C>T maps to NM_206862.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:792031 C>T maps to NM_001191061.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:792031 C>T maps to NM_001191061.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:55433538 C>T maps to NM_001004704.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:55433538 C>T maps to NM_001004704.1 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:62289474 C>G maps to NM_001620.1 L4138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:62289474 C>G maps to NM_001620.1 L4138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:68207275 C>A maps to NM_002335.2 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr11:68207275 C>A maps to NM_002335.2 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:45810575 C>T maps to NM_001142679.1 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:45810575 C>T maps to NM_001142679.1 D702D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:46764359 C>G maps to NM_018976.4 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:46764359 C>G maps to NM_018976.4 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:124109398 C>A maps to NM_001414.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr12:124109398 C>A maps to NM_001414.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr13:70314530 A>G maps to NM_020866.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr13:70314530 A>G maps to NM_020866.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr14:75369020 C>G maps to NM_001933.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr14:75369020 C>G maps to NM_001933.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr14:105644072 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr14:105644072 C>T did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:1551482 C>T maps to NM_016111.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:1551482 C>T maps to NM_016111.3 D448D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:1877397 C>A maps to NM_001018104.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:1877397 C>A maps to NM_001018104.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:67242310 A>G maps to NM_001004055.1 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr16:67242310 A>G maps to NM_001004055.1 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr17:9631803 G>T maps to NM_153210.3 E957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr17:9631803 G>T maps to NM_153210.3 E957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr17:72691300 G>A maps to ENST00000412086 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr17:72691300 G>A maps to ENST00000412086 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr18:25593676 C>T maps to NM_001792.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr18:25593676 C>T maps to NM_001792.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr18:52946873 G>C maps to ENST00000398339 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr18:52946873 G>C maps to ENST00000398339 S290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:2852821 G>A maps to NM_152791.4 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:2852821 G>A maps to NM_152791.4 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:21281117 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:21281117 G>A did not map to a codon.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:44891095 G>A maps to NM_152354.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:44891095 G>A maps to NM_152354.3 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:53994368 G>T maps to NM_001004301.3 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:53994368 G>T maps to NM_001004301.3 G295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:55493696 C>T maps to NM_017852.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr19:55493696 C>T maps to NM_017852.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:256640 G>C maps to NM_153269.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:256640 G>C maps to NM_153269.1 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:32336847 G>A maps to ENST00000375200 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:32336847 G>A maps to ENST00000375200 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:36758656 C>T maps to NM_004613.2 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:36758656 C>T maps to NM_004613.2 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:57767954 G>T maps to NM_178457.1 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr20:57767954 G>T maps to NM_178457.1 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr21:47674340 C>T maps to NM_003906.3 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr21:47674340 C>T maps to NM_003906.3 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr22:29730358 G>C maps to NM_001127.3 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A13J-01A-11D-A10S-08 chr22:29730358 G>C maps to NM_001127.3 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:35919961 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:35919961 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:89637585 C>A maps to NM_207398.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:89637585 C>A maps to NM_207398.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:114308927 A>G maps to NM_018364.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:114308927 A>G maps to NM_018364.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:243668580 T>C maps to NM_005465.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr1:243668580 T>C maps to NM_005465.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr2:179475789 G>A maps to NM_133378.4 A14454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr2:179475789 G>A maps to NM_133378.4 A14454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr3:50324240 G>A maps to NM_153215.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr3:50324240 G>A maps to NM_153215.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:90857416 G>A maps to NM_007351.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:90857416 G>A maps to NM_007351.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:143159108 C>T maps to NM_003866.2 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:143159108 C>T maps to NM_003866.2 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:175899048 G>A maps to NM_014269.4 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr4:175899048 G>A maps to NM_014269.4 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:50137808 C>T maps to ENST00000505697 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:50137808 C>T maps to ENST00000505697 D825D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:160721254 G>A maps to NM_021911.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr5:160721254 G>A maps to NM_021911.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr8:113678639 T>A maps to NM_198123.1 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr8:113678639 T>A maps to NM_198123.1 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr11:77924750 G>T maps to NM_020798.2 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr11:77924750 G>T maps to NM_020798.2 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr12:53012080 G>A maps to NM_175068.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr12:53012080 G>A maps to NM_175068.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr15:72030240 C>T maps to NM_024817.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr15:72030240 C>T maps to NM_024817.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr16:703598 G>A maps to NM_145294.4 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr16:703598 G>A maps to NM_145294.4 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr16:16297361 C>T maps to NM_001171.5 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr16:16297361 C>T maps to NM_001171.5 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr17:16593761 G>A maps to NM_014695.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr17:16593761 G>A maps to NM_014695.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr19:2098099 C>T maps to NM_001039846.1 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr19:2098099 C>T maps to NM_001039846.1 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr19:54327326 G>A maps to ENST00000391773 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0S7-01A-11D-A10S-08 chr19:54327326 G>A maps to ENST00000391773 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:12333104 C>T maps to NM_015378.2 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:12333104 C>T maps to NM_015378.2 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17395562 G>A maps to NM_007365.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17395562 G>A maps to NM_007365.2 F658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17395643 G>A maps to NM_007365.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17395643 G>A maps to NM_007365.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17575709 C>A maps to NM_016233.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:17575709 C>A maps to NM_016233.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:43893962 G>A maps to NM_015284.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:43893962 G>A maps to NM_015284.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:55136237 G>C maps to ENST00000454855 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:55136237 G>C maps to ENST00000454855 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:60336746 G>T maps to NM_015888.4 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:60336746 G>T maps to NM_015888.4 E661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:78163602 A>G maps to NM_015017.3 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:78163602 A>G maps to NM_015017.3 P872P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:93649604 C>T maps to NM_206886.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:93649604 C>T maps to NM_206886.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:113460505 C>T maps to NM_003051.3 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:113460505 C>T maps to NM_003051.3 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:151498240 G>T maps to NM_020770.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:151498240 G>T maps to NM_020770.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:152083886 C>T maps to NM_007113.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:152083886 C>T maps to NM_007113.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:155172608 G>A maps to NM_007112.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:155172608 G>A maps to NM_007112.3 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:161166036 G>A maps to NM_005099.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:161166036 G>A maps to NM_005099.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:171621259 C>T maps to NM_000261.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:171621259 C>T maps to NM_000261.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:180775196 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:180775196 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:183194781 G>A maps to NM_005562.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:183194781 G>A maps to NM_005562.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:202411573 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:202411573 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:203453265 C>G maps to NM_201348.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:203453265 C>G maps to NM_201348.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:204379759 C>A maps to NM_032833.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:204379759 C>A maps to NM_032833.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:235357526 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:235357526 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:243328907 G>C maps to NM_014812.2 S785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:243328907 G>C maps to NM_014812.2 S785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:37319355 C>G maps to ENST00000379187 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:37319355 C>G maps to ENST00000379187 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:74699246 C>A maps to NM_053050.3 *113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:74699246 C>A maps to NM_053050.3 *113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:96952860 G>A maps to NM_014014.3 I1174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:96952860 G>A maps to NM_014014.3 I1174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:100011208 G>C maps to NM_015904.3 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:100011208 G>C maps to NM_015904.3 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:103119998 C>T maps to NM_001011552.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:103119998 C>T maps to NM_001011552.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:127453716 G>A maps to NM_002101.3 *129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:127453716 G>A maps to NM_002101.3 *129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:136467038 A>G maps to ENST00000409606 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:136467038 A>G maps to ENST00000409606 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:170083084 G>A maps to NM_004525.2 F1747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:170083084 G>A maps to NM_004525.2 F1747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:170367163 G>A maps to NM_006063.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:170367163 G>A maps to NM_006063.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:223389718 C>T maps to NM_152386.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:223389718 C>T maps to NM_152386.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:227662878 G>A maps to NM_005544.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:227662878 G>A maps to NM_005544.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:227663124 G>C maps to NM_005544.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:227663124 G>C maps to NM_005544.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:230656621 G>A maps to ENST00000389044 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:230656621 G>A maps to ENST00000389044 L1432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:240061421 C>T maps to NM_006037.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr2:240061421 C>T maps to NM_006037.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:13393438 G>C maps to NM_024923.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:13393438 G>C maps to NM_024923.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:28381982 G>A maps to NM_022461.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:28381982 G>A maps to NM_022461.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:33458291 C>G maps to NM_001128161.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:33458291 C>G maps to NM_001128161.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:38921614 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:38921614 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:48423543 G>T maps to NM_207102.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:48423543 G>T maps to NM_207102.2 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:48641042 G>A maps to NM_003365.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:48641042 G>A maps to NM_003365.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:50391173 G>C maps to NM_007022.3 *223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:50391173 G>C maps to NM_007022.3 *223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:53157762 C>T maps to NM_052859.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:53157762 C>T maps to NM_052859.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:53326413 C>T maps to ENST00000480258 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:53326413 C>T maps to ENST00000480258 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:56647735 G>A maps to NM_001141947.1 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:56647735 G>A maps to NM_001141947.1 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:101390112 G>A maps to NM_014415.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:101390112 G>A maps to NM_014415.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:105438983 G>A maps to NM_170662.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:105438983 G>A maps to NM_170662.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:129282029 G>A maps to NM_015103.2 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:129282029 G>A maps to NM_015103.2 I1525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:140185545 C>T maps to NM_022131.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:140185545 C>T maps to NM_022131.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:160156856 G>A maps to ENST00000483754 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:160156856 G>A maps to ENST00000483754 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:167759262 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:167759262 C>G did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:184009971 C>T maps to NM_014693.3 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:184009971 C>T maps to NM_014693.3 F866F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:186299203 G>A maps to NM_016306.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr3:186299203 G>A maps to NM_016306.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:3208287 C>T maps to NM_002111.6 I1928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:3208287 C>T maps to NM_002111.6 I1928I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:48901919 G>C maps to NM_001014446.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:48901919 G>C maps to NM_001014446.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:110442740 C>T maps to NM_006323.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:110442740 C>T maps to NM_006323.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:126371890 C>G maps to NM_024582.4 L3240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:126371890 C>G maps to NM_024582.4 L3240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:128938604 G>A maps to ENST00000454347 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:128938604 G>A maps to ENST00000454347 E186E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:160260432 G>T maps to NM_014247.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr4:160260432 G>T maps to NM_014247.2 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:1064230 G>C maps to NM_006598.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:1064230 G>C maps to NM_006598.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:1221313 C>T maps to NM_001003841.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:1221313 C>T maps to NM_001003841.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:10403538 G>C maps to NM_005885.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:10403538 G>C maps to NM_005885.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:68412386 G>A maps to NM_022902.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:68412386 G>A maps to NM_022902.2 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:71491836 C>T maps to NM_005909.3 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:71491836 C>T maps to NM_005909.3 T885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:90449159 G>A maps to NM_032119.3 L6249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:90449159 G>A maps to NM_032119.3 L6249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:110818484 C>T maps to NM_001744.4 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:110818484 C>T maps to NM_001744.4 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:112769840 G>A maps to NM_032028.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:112769840 G>A maps to NM_032028.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:140763129 C>T maps to NM_018920.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:140763129 C>T maps to NM_018920.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:151231106 C>G maps to NM_001146040.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:151231106 C>G maps to NM_001146040.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:172386932 C>T maps to NM_016093.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr5:172386932 C>T maps to NM_016093.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:7231403 C>T maps to NM_001003699.3 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:7231403 C>T maps to NM_001003699.3 V1024V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:31609348 G>A maps to ENST00000404765 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:31609348 G>A maps to ENST00000404765 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:31710891 G>A maps to ENST00000375742 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:31710891 G>A maps to ENST00000375742 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:33660623 G>A maps to ENST00000374316 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:33660623 G>A maps to ENST00000374316 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:38957822 C>T maps to ENST00000327475 F4351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:38957822 C>T maps to ENST00000327475 F4351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:43114420 C>T maps to NM_002821.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:43114420 C>T maps to NM_002821.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:44310890 C>G maps to NM_145026.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:44310890 C>G maps to NM_145026.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:51929768 G>A maps to NM_138694.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:51929768 G>A maps to NM_138694.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:126320718 G>A maps to NM_001031712.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:126320718 G>A maps to NM_001031712.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:134210741 G>A maps to NM_003206.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr6:134210741 G>A maps to NM_003206.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:4830467 G>C maps to ENST00000450194 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:4830467 G>C maps to ENST00000450194 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:99170384 G>A maps to NM_001083956.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:99170384 G>A maps to NM_001083956.1 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:99170441 G>A maps to NM_001083956.1 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:99170441 G>A maps to NM_001083956.1 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:100695123 C>T maps to NM_001040105.1 F4328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:100695123 C>T maps to NM_001040105.1 F4328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:127714729 G>A maps to NM_014390.2 Q652Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:127714729 G>A maps to NM_014390.2 Q652Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:132754903 G>C maps to ENST00000448878 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:132754903 G>C maps to ENST00000448878 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:149463158 C>A maps to NM_207336.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr7:149463158 C>A maps to NM_207336.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:22487502 C>T maps to NM_018688.4 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:22487502 C>T maps to NM_018688.4 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:39806666 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:39806666 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:43211962 C>G maps to NM_001005365.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:43211962 C>G maps to NM_001005365.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:75262800 C>T maps to NM_018972.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:75262800 C>T maps to NM_018972.2 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:99440458 C>T maps to NM_020697.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:99440458 C>T maps to NM_020697.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:144732815 G>T maps to NM_014789.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr8:144732815 G>T maps to NM_014789.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:16435865 C>A maps to NM_017637.5 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:16435865 C>A maps to NM_017637.5 E776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:35736617 C>G maps to NM_006368.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:35736617 C>G maps to NM_006368.4 L337L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A0YX-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BT-A0YX-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:98691086 C>G maps to NM_001010895.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:98691086 C>G maps to NM_001010895.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:101825365 C>G maps to NM_001855.3 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:101825365 C>G maps to NM_001855.3 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:111741737 C>T maps to NM_003798.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:111741737 C>T maps to NM_003798.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:116131968 G>A maps to NM_017688.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:116131968 G>A maps to NM_017688.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:130829326 C>T maps to NM_197956.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:130829326 C>T maps to NM_197956.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:131517772 G>A maps to NM_006336.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:131517772 G>A maps to NM_006336.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:131709435 G>C maps to NM_014908.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:131709435 G>C maps to NM_014908.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:138395831 C>G maps to NM_016034.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:138395831 C>G maps to NM_016034.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:138669287 C>T maps to ENST00000298480 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr9:138669287 C>T maps to ENST00000298480 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:6143280 G>A maps to NM_001145547.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:6143280 G>A maps to NM_001145547.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:23408325 G>A maps to ENST00000277598 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:23408325 G>A maps to ENST00000277598 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:33200925 G>A maps to ENST00000374956 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:33200925 G>A maps to ENST00000374956 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:33224453 C>T maps to ENST00000374956 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:33224453 C>T maps to ENST00000374956 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:73122190 C>T maps to NM_018344.5 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:73122190 C>T maps to NM_018344.5 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:75574820 G>C maps to ENST00000423381 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:75574820 G>C maps to ENST00000423381 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:105903396 C>T maps to ENST00000389588 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:105903396 C>T maps to ENST00000389588 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:124152832 C>T maps to NM_021622.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:124152832 C>T maps to NM_021622.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:124358520 C>G maps to ENST00000368915 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:124358520 C>G maps to ENST00000368915 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:127429113 G>A maps to ENST00000356792 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr10:127429113 G>A maps to ENST00000356792 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:46727043 C>G maps to NM_024741.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:46727043 C>G maps to NM_024741.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:47858483 G>A maps to NM_015231.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:47858483 G>A maps to NM_015231.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:56757050 C>T maps to NM_001005323.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:56757050 C>T maps to NM_001005323.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:60610304 G>A maps to NM_024098.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:60610304 G>A maps to NM_024098.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:61644426 G>C maps to NM_021727.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:61644426 G>C maps to NM_021727.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:62288784 G>C maps to NM_001620.1 L4368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:62288784 G>C maps to NM_001620.1 L4368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:65341110 G>A maps to NM_001098785.1 *190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:65341110 G>A maps to NM_001098785.1 *190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:66460710 C>T maps to NM_006946.2 A1600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:66460710 C>T maps to NM_006946.2 A1600A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:67172955 G>A maps to NM_198517.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:67172955 G>A maps to NM_198517.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:70049612 G>A maps to NM_003824.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:70049612 G>A maps to NM_003824.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:102100668 T>C maps to NM_001130145.2 *505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:102100668 T>C maps to NM_001130145.2 *505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:113697973 G>A maps to NM_020886.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:113697973 G>A maps to NM_020886.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:124310897 G>A maps to NM_012378.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:124310897 G>A maps to NM_012378.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:124482953 C>A maps to NM_052959.2 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:124482953 C>A maps to NM_052959.2 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:126139116 C>T maps to NM_017547.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:126139116 C>T maps to NM_017547.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:128781854 C>T maps to NM_000890.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr11:128781854 C>T maps to NM_000890.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:5020927 G>A maps to NM_000217.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:5020927 G>A maps to NM_000217.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:6690249 C>G maps to ENST00000309577 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:6690249 C>G maps to ENST00000309577 V1651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:21680079 G>A maps to NM_030572.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:21680079 G>A maps to NM_030572.2 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:27066550 C>T maps to NM_018164.2 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:27066550 C>T maps to NM_018164.2 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:48369178 G>A maps to NM_001844.4 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:48369178 G>A maps to NM_001844.4 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:53911119 G>C maps to NM_001130059.1 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:53911119 G>C maps to NM_001130059.1 S429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:54756621 G>A maps to NM_020370.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:54756621 G>A maps to NM_020370.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:56868839 G>C maps to NM_013267.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:56868839 G>C maps to NM_013267.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:75900672 C>T maps to NM_007043.6 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:75900672 C>T maps to NM_007043.6 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:78225382 G>T maps to NM_014903.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:78225382 G>T maps to NM_014903.4 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:110463572 G>A maps to NM_033121.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:110463572 G>A maps to NM_033121.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:121882021 G>C maps to ENST00000377071 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:121882021 G>C maps to ENST00000377071 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:130830391 G>A maps to NM_004764.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:130830391 G>A maps to NM_004764.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:131498797 G>A maps to NM_198827.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr12:131498797 G>A maps to NM_198827.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:36229745 G>A maps to ENST00000400445 W2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:36229745 G>A maps to ENST00000400445 W2720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:41515450 G>A maps to NM_172373.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:41515450 G>A maps to NM_172373.3 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:50299569 G>A maps to NM_002267.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:50299569 G>A maps to NM_002267.3 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:92560197 C>T maps to NM_004466.4 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:92560197 C>T maps to NM_004466.4 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:103298649 G>A maps to ENST00000376052 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr13:103298649 G>A maps to ENST00000376052 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:20841486 G>A maps to NM_007110.4 L2252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:20841486 G>A maps to NM_007110.4 L2252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:20978928 C>G maps to ENST00000430083 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:20978928 C>G maps to ENST00000430083 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:31574847 G>C maps to NM_015382.2 S2418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:31574847 G>C maps to NM_015382.2 S2418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:51196369 C>T maps to NM_020921.3 Q1983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:51196369 C>T maps to NM_020921.3 Q1983Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:51204914 C>T maps to NM_020921.3 L1906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:51204914 C>T maps to NM_020921.3 L1906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:74824669 C>G maps to NM_018228.2 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:74824669 C>G maps to NM_018228.2 S395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:76249832 C>T maps to NM_015072.4 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:76249832 C>T maps to NM_015072.4 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:77492254 G>C maps to NM_024496.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:77492254 G>C maps to NM_024496.2 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:96807894 G>A maps to NM_018036.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:96807894 G>A maps to NM_018036.5 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:96912856 G>C maps to NM_152327.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:96912856 G>C maps to NM_152327.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:104026369 C>A maps to NM_001015049.2 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:104026369 C>A maps to NM_001015049.2 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:104037963 C>G maps to ENST00000445352 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:104037963 C>G maps to ENST00000445352 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:105177450 C>T maps to ENST00000252520 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr14:105177450 C>T maps to ENST00000252520 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:42462050 C>T maps to ENST00000348544 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:42462050 C>T maps to ENST00000348544 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:42568596 C>T maps to NM_198141.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:42568596 C>T maps to NM_198141.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:43873499 C>T maps to NM_001130858.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:43873499 C>T maps to NM_001130858.2 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:53908308 G>C maps to NM_182758.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:53908308 G>C maps to NM_182758.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:65255978 G>A maps to NM_016630.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr15:65255978 G>A maps to NM_016630.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:2159440 G>A maps to NM_001009944.2 I1909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:2159440 G>A maps to NM_001009944.2 I1909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:2570862 G>A maps to NM_001145815.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:2570862 G>A maps to NM_001145815.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:3273996 C>T maps to NM_198088.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:3273996 C>T maps to NM_198088.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:3339454 C>T maps to NM_005741.4 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:3339454 C>T maps to NM_005741.4 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:4412078 G>A maps to NM_024535.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:4412078 G>A maps to NM_024535.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:4933744 C>T maps to NM_002705.4 Q1637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:4933744 C>T maps to NM_002705.4 Q1637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:31195650 C>T maps to NM_004960.3 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:31195650 C>T maps to NM_004960.3 Q153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:50346029 G>A maps to NM_001114.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:50346029 G>A maps to NM_001114.3 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:67662355 G>A maps to NM_006565.3 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:67662355 G>A maps to NM_006565.3 Q534Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:75512841 G>A maps to NM_021615.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:75512841 G>A maps to NM_021615.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:81934315 G>A maps to NM_002661.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:81934315 G>A maps to NM_002661.2 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:89598328 C>G maps to NM_003119.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr16:89598328 C>G maps to NM_003119.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:3458045 C>T maps to ENST00000381913 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:3458045 C>T maps to ENST00000381913 E33E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4544956 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4544956 G>C did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4904540 C>T maps to NM_006612.5 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4904540 C>T maps to NM_006612.5 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4905848 C>T maps to NM_006612.5 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4905848 C>T maps to NM_006612.5 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4925874 C>G maps to NM_006612.5 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:4925874 C>G maps to NM_006612.5 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:17116969 C>G maps to NM_144997.5 *580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:17116969 C>G maps to NM_144997.5 *580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:27945891 C>T maps to ENST00000345068 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:27945891 C>T maps to ENST00000345068 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:31318968 C>T maps to NM_173847.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:31318968 C>T maps to NM_173847.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:35872726 C>G maps to NM_007026.2 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:35872726 C>G maps to NM_007026.2 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:38319904 C>T maps to NM_007359.4 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:38319904 C>T maps to NM_007359.4 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:38711548 G>C maps to NM_001838.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:38711548 G>C maps to NM_001838.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:40260105 C>T maps to NM_024119.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:40260105 C>T maps to NM_024119.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:41477528 G>A maps to NM_001661.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:41477528 G>A maps to NM_001661.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:66270074 G>A maps to NM_004694.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:66270074 G>A maps to NM_004694.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:76171136 C>T maps to NM_003258.4 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:76171136 C>T maps to NM_003258.4 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:78353430 G>A maps to NM_020914.4 P4568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr17:78353430 G>A maps to NM_020914.4 P4568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:2892353 G>A maps to NM_032048.2 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:2892353 G>A maps to NM_032048.2 Q743Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:3508615 G>C maps to NM_004746.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:3508615 G>C maps to NM_004746.2 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:7023259 C>T maps to NM_005559.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr18:7023259 C>T maps to NM_005559.2 G868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:1111583 G>A maps to NM_014963.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:1111583 G>A maps to NM_014963.2 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:2116612 C>T maps to ENST00000355272 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:2116612 C>T maps to ENST00000355272 E664E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:7591754 C>T maps to NM_020533.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:7591754 C>T maps to NM_020533.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:8503336 G>A maps to NM_016496.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:8503336 G>A maps to NM_016496.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:8999055 G>A maps to NM_024690.2 F13596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:8999055 G>A maps to NM_024690.2 F13596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:10221061 G>A maps to NM_001040664.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:10221061 G>A maps to NM_001040664.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:10692041 C>T maps to ENST00000453102 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:10692041 C>T maps to ENST00000453102 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:17000939 C>T maps to NM_003950.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:17000939 C>T maps to NM_003950.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:39008107 G>A maps to NM_000540.2 E3265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:39008107 G>A maps to NM_000540.2 E3265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:39061260 G>A maps to NM_000540.2 R4558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:39061260 G>A maps to NM_000540.2 R4558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:44537160 C>G maps to NM_001129996.1 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:44537160 C>G maps to NM_001129996.1 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:54746130 C>T maps to ENST00000407860 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:54746130 C>T maps to ENST00000407860 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:55610163 C>A maps to NM_017607.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:55610163 C>A maps to NM_017607.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:55689629 C>T maps to NM_003180.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:55689629 C>T maps to NM_003180.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:57932475 C>G maps to NM_006959.2 S539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:57932475 C>G maps to NM_006959.2 S539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:58982926 C>G maps to NM_014347.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:58982926 C>G maps to NM_014347.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:25295600 C>G maps to NM_015600.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:25295600 C>G maps to NM_015600.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:31760843 C>T maps to NM_080574.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:31760843 C>T maps to NM_080574.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:36488326 C>T maps to NM_030877.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:36488326 C>T maps to NM_030877.3 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:43850713 G>A maps to NM_003008.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:43850713 G>A maps to NM_003008.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:48130896 G>C maps to NM_000961.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr20:48130896 G>C maps to NM_000961.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr21:15561576 G>A maps to NM_198996.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr21:15561576 G>A maps to NM_198996.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr21:45518305 C>G maps to NM_003274.4 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr21:45518305 C>G maps to NM_003274.4 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:18566265 C>T maps to NM_017929.5 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:18566265 C>T maps to NM_017929.5 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:24086953 G>C maps to NM_021916.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:24086953 G>C maps to NM_021916.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:27003913 C>T maps to NM_001887.3 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:27003913 C>T maps to NM_001887.3 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:29752416 C>T maps to NM_001127.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:29752416 C>T maps to NM_001127.3 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:30188507 G>A maps to NM_032204.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:30188507 G>A maps to NM_032204.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:37770272 G>A maps to NM_052906.3 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:37770272 G>A maps to NM_052906.3 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:45818176 C>T maps to NM_015653.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:45818176 C>T maps to NM_015653.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:46693368 G>A maps to NM_016426.6 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:46693368 G>A maps to NM_016426.6 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:50721498 G>A maps to NM_012401.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr22:50721498 G>A maps to NM_012401.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:2876406 G>A maps to NM_000047.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:2876406 G>A maps to NM_000047.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:18926149 G>C maps to NM_000292.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:18926149 G>C maps to NM_000292.2 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:32429879 G>A maps to ENST00000357033 Q1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:32429879 G>A maps to ENST00000357033 Q1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:40568681 C>G maps to NM_004229.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:40568681 C>G maps to NM_004229.3 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:53587225 C>T maps to ENST00000276009 L2553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:53587225 C>T maps to ENST00000276009 L2553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:54781510 C>T maps to NM_198510.2 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:54781510 C>T maps to NM_198510.2 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:54956579 T>C maps to NM_001039705.1 G1141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:54956579 T>C maps to NM_001039705.1 G1141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:102974113 G>C maps to NM_001024452.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:102974113 G>C maps to NM_001024452.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:109695176 C>G maps to NM_020769.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:109695176 C>G maps to NM_020769.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:129185833 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:129185833 G>A did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:151303654 G>C maps to NM_021048.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:151303654 G>C maps to NM_021048.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:153040416 G>A maps to NM_005393.2 E1338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:153040416 G>A maps to NM_005393.2 E1338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:153577784 C>T maps to NM_001110556.1 L2567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chrX:153577784 C>T maps to NM_001110556.1 L2567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:4772145 G>A maps to NM_018836.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:4772145 G>A maps to NM_018836.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:17413061 G>C maps to NM_007365.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:17413061 G>C maps to NM_007365.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:21307590 G>A maps to NM_001198801.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:21307590 G>A maps to NM_001198801.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:27087920 C>T maps to NM_006015.4 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:27087920 C>T maps to NM_006015.4 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:39827346 C>T maps to ENST00000361689 Q2195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:39827346 C>T maps to ENST00000361689 Q2195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:151861805 G>A maps to NM_053055.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:151861805 G>A maps to NM_053055.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:153906267 C>G maps to NM_014856.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:153906267 C>G maps to NM_014856.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:155319162 C>T maps to ENST00000368346 V2508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:155319162 C>T maps to ENST00000368346 V2508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:173839951 C>T maps to NM_001122770.1 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:173839951 C>T maps to NM_001122770.1 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:173839956 C>T maps to NM_001122770.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr1:173839956 C>T maps to NM_001122770.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:10126391 C>T maps to NM_198182.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:10126391 C>T maps to NM_198182.2 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:24011421 G>C maps to NM_017552.1 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:24011421 G>C maps to NM_017552.1 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:30976030 G>A maps to ENST00000295055 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:30976030 G>A maps to ENST00000295055 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:33412109 C>T maps to ENST00000354476 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:33412109 C>T maps to ENST00000354476 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:37283641 G>C maps to NM_019024.1 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:37283641 G>C maps to NM_019024.1 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:42996987 G>C maps to NM_012205.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:42996987 G>C maps to NM_012205.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:88874948 G>A maps to NM_004836.5 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:88874948 G>A maps to NM_004836.5 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:97276602 G>C maps to ENST00000421845 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:97276602 G>C maps to ENST00000421845 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:108479194 G>T maps to NM_182588.2 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:108479194 G>T maps to NM_182588.2 E755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740455 G>A maps to NM_006343.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740455 G>A maps to NM_006343.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740500 G>A maps to NM_006343.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740500 G>A maps to NM_006343.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740536 G>C maps to NM_006343.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:112740536 G>C maps to NM_006343.2 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:130738131 G>A maps to NM_032144.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:130738131 G>A maps to NM_032144.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:145161506 C>T maps to NM_014795.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:145161506 C>T maps to NM_014795.3 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:165947271 C>T maps to NM_006922.3 W1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:165947271 C>T maps to NM_006922.3 W1797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:170506886 T>C maps to NM_001085447.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:170506886 T>C maps to NM_001085447.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:187516804 C>G maps to NM_002210.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:187516804 C>G maps to NM_002210.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:198498568 C>T maps to NM_144629.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:198498568 C>T maps to NM_144629.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:201468753 C>T maps to NM_001159.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:201468753 C>T maps to NM_001159.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:203420556 C>T maps to NM_001204.6 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:203420556 C>T maps to NM_001204.6 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:239184477 C>T maps to NM_022817.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:239184477 C>T maps to NM_022817.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:241468764 G>T maps to ENST00000401804 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr2:241468764 G>T maps to ENST00000401804 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:3189209 G>A maps to NM_182916.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:3189209 G>A maps to NM_182916.2 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:15124115 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:15124115 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:42573762 C>T maps to NM_004624.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:42573762 C>T maps to NM_004624.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:49933756 C>T maps to NM_002447.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:49933756 C>T maps to NM_002447.2 G840G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:52264888 C>T maps to ENST00000494383 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:52264888 C>T maps to ENST00000494383 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:53212458 C>T maps to NM_212539.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:53212458 C>T maps to NM_212539.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:112546397 C>T maps to NM_001008784.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:112546397 C>T maps to NM_001008784.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:113528246 G>A maps to NM_001690.3 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:113528246 G>A maps to NM_001690.3 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:121206873 G>C maps to ENST00000393672 S1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:121206873 G>C maps to ENST00000393672 S1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:127831850 G>A maps to NM_003707.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:127831850 G>A maps to NM_003707.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:133494391 C>T maps to NM_001063.3 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:133494391 C>T maps to NM_001063.3 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:155232673 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:155232673 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:158384152 G>T maps to ENST00000264263 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:158384152 G>T maps to ENST00000264263 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:167414890 G>A maps to NM_145859.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:167414890 G>A maps to NM_145859.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:183860564 A>C did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:183860564 A>C did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:185191488 C>T maps to NM_004721.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr3:185191488 C>T maps to NM_004721.3 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:435804 C>T maps to NM_133474.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:435804 C>T maps to NM_133474.2 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:78527048 C>T maps to NM_006419.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:78527048 C>T maps to NM_006419.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:86893234 C>T maps to NM_001025616.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:86893234 C>T maps to NM_001025616.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:100479302 G>C maps to NM_001134666.1 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:100479302 G>C maps to NM_001134666.1 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:110882117 C>T maps to NM_001963.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:110882117 C>T maps to NM_001963.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:121738026 G>A maps to NM_018699.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:121738026 G>A maps to NM_018699.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:183664473 G>A maps to NM_001080477.1 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr4:183664473 G>A maps to NM_001080477.1 A1177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:1076836 G>A maps to NM_006598.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:1076836 G>A maps to NM_006598.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:5476187 G>C maps to NM_015325.1 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:5476187 G>C maps to NM_015325.1 L2172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:37371139 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:37371139 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:79950602 G>A maps to NM_002439.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:79950602 G>A maps to NM_002439.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:96349454 C>T maps to NM_005575.2 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:96349454 C>T maps to NM_005575.2 I713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:96503504 C>A maps to NM_018343.2 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:96503504 C>A maps to NM_018343.2 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140167236 G>A maps to NM_018900.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140167236 G>A maps to NM_018900.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140574014 G>A maps to NM_018930.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140574014 G>A maps to NM_018930.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140712086 C>T maps to NM_018912.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr5:140712086 C>T maps to NM_018912.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:3850758 C>T maps to NM_012135.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:3850758 C>T maps to NM_012135.1 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:4049305 C>G maps to NM_003913.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:4049305 C>G maps to NM_003913.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:26252141 G>C maps to NM_003524.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:26252141 G>C maps to NM_003524.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:30457337 C>G maps to NM_005516.5 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:30457337 C>G maps to NM_005516.5 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:32016365 C>T maps to ENST00000375244 V3273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:32016365 C>T maps to ENST00000375244 V3273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:41011325 G>C maps to NM_001159726.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:41011325 G>C maps to NM_001159726.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:46801037 C>T maps to NM_005588.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:46801037 C>T maps to NM_005588.2 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:52268301 C>T maps to ENST00000361841 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:52268301 C>T maps to ENST00000361841 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:107035676 G>C maps to NM_032730.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:107035676 G>C maps to NM_032730.4 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:136977456 C>G maps to NM_005923.3 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:136977456 C>G maps to NM_005923.3 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:144803391 C>T maps to NM_007124.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:144803391 C>T maps to NM_007124.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:151742432 C>T maps to NM_017909.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr6:151742432 C>T maps to NM_017909.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:106509784 T>C maps to NM_002649.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:106509784 T>C maps to NM_002649.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:114304339 G>T maps to NM_148898.3 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:114304339 G>T maps to NM_148898.3 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:116436027 C>T maps to NM_001127500.1 F1359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:116436027 C>T maps to NM_001127500.1 F1359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:138863035 C>G maps to NM_024926.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr7:138863035 C>G maps to NM_024926.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:18622976 G>A maps to ENST00000440756 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:18622976 G>A maps to ENST00000440756 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:21926965 C>T maps to ENST00000265800 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:21926965 C>T maps to ENST00000265800 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:23112845 C>T maps to NM_152272.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:23112845 C>T maps to NM_152272.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:66619458 G>A maps to NM_014637.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:66619458 G>A maps to NM_014637.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:126448547 C>G maps to NM_025195.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:126448547 C>G maps to NM_025195.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:128750660 G>A maps to NM_002467.4 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:128750660 G>A maps to NM_002467.4 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:144943482 C>G maps to NM_031308.1 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr8:144943482 C>G maps to NM_031308.1 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:74319521 G>C maps to NM_013390.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:74319521 G>C maps to NM_013390.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:94486309 G>A maps to NM_004560.2 N822N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:94486309 G>A maps to NM_004560.2 N822N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:94809521 G>T maps to NM_006415.2 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:94809521 G>T maps to NM_006415.2 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:100079487 G>T maps to ENST00000375206 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:100079487 G>T maps to ENST00000375206 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:115805728 G>C maps to NM_003408.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:115805728 G>C maps to NM_003408.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:119770437 T>G maps to ENST00000313400 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:119770437 T>G maps to ENST00000313400 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:138903718 G>A maps to NM_144653.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:138903718 G>A maps to NM_144653.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:139371367 C>A maps to NM_014866.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr9:139371367 C>A maps to NM_014866.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:29820208 G>C maps to NM_021738.2 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:29820208 G>C maps to NM_021738.2 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:49632596 C>T maps to NM_139047.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:49632596 C>T maps to NM_139047.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:81701776 G>A maps to NM_003019.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:81701776 G>A maps to NM_003019.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:111640656 G>A maps to NM_020383.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:111640656 G>A maps to NM_020383.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:115947865 C>T maps to NM_198795.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr10:115947865 C>T maps to NM_198795.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:771390 G>A maps to NM_182612.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:771390 G>A maps to NM_182612.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:16812670 G>A maps to ENST00000448080 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:16812670 G>A maps to ENST00000448080 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:62296059 C>A maps to NM_001620.1 S1943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:62296059 C>A maps to NM_001620.1 S1943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:68703930 C>T maps to NM_002180.2 H661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:68703930 C>T maps to NM_002180.2 H661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:72945965 C>T maps to NM_176071.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:72945965 C>T maps to NM_176071.1 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:72945971 C>G maps to NM_176071.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:72945971 C>G maps to NM_176071.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:73627687 G>A maps to NM_025155.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:73627687 G>A maps to NM_025155.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:93778979 G>A maps to NM_001098672.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:93778979 G>A maps to NM_001098672.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:106849345 G>A maps to ENST00000282249 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:106849345 G>A maps to ENST00000282249 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:113210176 G>C maps to NM_017868.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:113210176 G>C maps to NM_017868.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:113651014 C>G maps to NM_001101389.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:113651014 C>G maps to NM_001101389.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:123893844 C>A maps to NM_001001953.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:123893844 C>A maps to NM_001001953.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:123909582 G>T maps to NM_001004463.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:123909582 G>T maps to NM_001004463.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:134244147 G>T maps to NM_138342.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:134244147 G>T maps to NM_138342.3 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:6710689 G>T maps to ENST00000309577 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:6710689 G>T maps to ENST00000309577 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:10959333 C>T maps to NM_023918.1 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:10959333 C>T maps to NM_023918.1 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:11339183 G>A maps to NM_181429.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:11339183 G>A maps to NM_181429.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:54448005 G>A maps to NM_153633.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:54448005 G>A maps to NM_153633.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:105601807 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:105601807 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:112609067 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:112609067 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:120241074 C>A maps to ENST00000392521 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:120241074 C>A maps to ENST00000392521 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:132380332 G>A maps to NM_003565.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr12:132380332 G>A maps to NM_003565.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:41507793 G>A maps to NM_172373.3 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:41507793 G>A maps to NM_172373.3 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:43643081 G>A maps to NM_013238.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:43643081 G>A maps to NM_013238.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:45147766 G>C maps to NM_183422.2 S815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:45147766 G>C maps to NM_183422.2 S815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:46656652 G>A maps to NM_001872.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:46656652 G>A maps to NM_001872.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:58299160 C>A maps to NM_001040429.2 Y1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:58299160 C>A maps to NM_001040429.2 Y1071*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:60348371 C>T maps to NM_001042517.1 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr13:60348371 C>T maps to NM_001042517.1 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:22133601 C>T maps to NM_001001912.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:22133601 C>T maps to NM_001001912.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:57270956 G>A maps to NM_021728.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:57270956 G>A maps to NM_021728.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:93693380 G>C maps to NM_175748.3 *426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:93693380 G>C maps to NM_175748.3 *426Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:94929549 C>T maps to NM_175739.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr14:94929549 C>T maps to NM_175739.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:1416390 G>A maps to ENST00000508903 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:1416390 G>A maps to ENST00000508903 I684I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:21063187 G>A maps to NM_017539.1 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:21063187 G>A maps to NM_017539.1 A1347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:21086797 C>T maps to NM_017539.1 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:21086797 C>T maps to NM_017539.1 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:27640095 G>A maps to NM_015202.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:27640095 G>A maps to NM_015202.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:66919263 G>A maps to NM_020786.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:66919263 G>A maps to NM_020786.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:67514905 G>C maps to NM_004691.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:67514905 G>C maps to NM_004691.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:86612412 C>G maps to NM_005250.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:86612412 C>G maps to NM_005250.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:87744969 C>T maps to NM_017566.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:87744969 C>T maps to NM_017566.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:89862343 G>A maps to NM_000135.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:89862343 G>A maps to NM_000135.2 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:89940209 C>T maps to NM_014972.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr16:89940209 C>T maps to NM_014972.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:1548931 G>A maps to NM_003693.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:1548931 G>A maps to NM_003693.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:3195372 C>T maps to ENST00000397187 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:3195372 C>T maps to ENST00000397187 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:10399383 C>T maps to NM_005963.3 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:10399383 C>T maps to NM_005963.3 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:16466490 C>G maps to NM_020653.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:16466490 C>G maps to NM_020653.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:26945943 C>A maps to NM_014680.2 L1896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:26945943 C>A maps to NM_014680.2 L1896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:38140721 C>T maps to NM_002809.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:38140721 C>T maps to NM_002809.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:43323890 C>T maps to NM_005892.3 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:43323890 C>T maps to NM_005892.3 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:48745048 C>G maps to NM_003786.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:48745048 C>G maps to NM_003786.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:57089712 C>A maps to NM_015294.3 G891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:57089712 C>A maps to NM_015294.3 G891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:68128890 C>G maps to NM_018658.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:68128890 C>G maps to NM_018658.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73205990 C>T maps to NM_024844.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73205990 C>T maps to NM_024844.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73554289 G>A maps to NM_001031803.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73554289 G>A maps to NM_001031803.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73623519 C>T maps to NM_004259.5 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr17:73623519 C>T maps to NM_004259.5 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr18:7024443 G>C maps to NM_005559.2 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr18:7024443 G>C maps to NM_005559.2 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:1440119 G>A maps to NM_001018.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:1440119 G>A maps to NM_001018.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2210631 G>T maps to ENST00000221482 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2210631 G>T maps to ENST00000221482 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2213596 G>A maps to ENST00000221482 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2213596 G>A maps to ENST00000221482 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2213855 G>A maps to ENST00000221482 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2213855 G>A maps to ENST00000221482 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2216698 G>A maps to ENST00000221482 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:2216698 G>A maps to ENST00000221482 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:4048049 G>A maps to NM_015898.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:4048049 G>A maps to NM_015898.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:16860124 C>T maps to ENST00000438489 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:16860124 C>T maps to ENST00000438489 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:36218435 G>C maps to NM_014727.1 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:36218435 G>C maps to NM_014727.1 L1405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:36322009 C>T maps to NM_004646.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:37211047 G>A maps to ENST00000423498 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:37211047 G>A maps to ENST00000423498 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:39361467 C>A maps to NM_001195833.1 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:39361467 C>A maps to NM_001195833.1 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:39521862 G>A maps to NM_178820.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:39521862 G>A maps to NM_178820.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:40902868 G>A maps to NM_181882.2 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:40902868 G>A maps to NM_181882.2 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:44235748 C>G maps to NM_019108.2 *521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:44235748 C>G maps to NM_019108.2 *521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:47425166 C>T maps to NM_004491.4 Q1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:47425166 C>T maps to NM_004491.4 Q1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:48892914 G>A maps to NM_006801.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:48892914 G>A maps to NM_006801.2 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49458851 C>T maps to NM_138761.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49458851 C>T maps to NM_138761.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49464128 C>T maps to NM_138761.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:49464128 C>T maps to NM_138761.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:52724376 C>T maps to NM_014225.5 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:52724376 C>T maps to NM_014225.5 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:55263167 C>G maps to NM_015868.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:55263167 C>G maps to NM_015868.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:55624148 C>T maps to NM_017607.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr19:55624148 C>T maps to NM_017607.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:4848511 G>A maps to NM_203327.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:4848511 G>A maps to NM_203327.1 F420F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:30137128 C>A maps to NM_178581.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:30137128 C>A maps to NM_178581.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:32379154 G>A maps to ENST00000375200 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:32379154 G>A maps to ENST00000375200 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:33632446 G>A maps to NM_015638.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:33632446 G>A maps to NM_015638.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:36982713 C>G maps to NM_004139.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:36982713 C>G maps to NM_004139.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:37357140 C>G maps to NM_080552.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:37357140 C>G maps to NM_080552.2 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:42164892 C>T maps to NM_032107.4 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr20:42164892 C>T maps to NM_032107.4 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:31655208 G>A maps to NM_001085455.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:31655208 G>A maps to NM_001085455.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:32519264 G>C maps to NM_003253.2 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:32519264 G>C maps to NM_003253.2 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:37595609 C>G maps to NM_005128.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:37595609 C>G maps to NM_005128.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:47359996 G>A maps to NM_020528.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr21:47359996 G>A maps to NM_020528.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:24468353 C>T maps to NM_012295.3 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:24468353 C>T maps to NM_012295.3 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:29835055 C>T maps to NM_021026.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:29835055 C>T maps to NM_021026.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:29921846 C>T maps to NM_003678.4 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:29921846 C>T maps to NM_003678.4 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:31266641 C>T maps to NM_030758.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:31266641 C>T maps to NM_030758.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:33255168 C>T maps to NM_000362.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr22:33255168 C>T maps to NM_000362.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:15349791 G>C maps to NM_002641.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:15349791 G>C maps to NM_002641.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:15548140 C>G maps to NM_203281.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:15548140 C>G maps to NM_203281.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:47069374 C>T maps to NM_153280.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:47069374 C>T maps to NM_153280.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:49030734 C>T maps to NM_002668.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chrX:49030734 C>T maps to NM_002668.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:11102930 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:11102930 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:12820736 C>G maps to NM_152290.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:12820736 C>G maps to NM_152290.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:12887574 T>A maps to NM_001146344.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:12887574 T>A maps to NM_001146344.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:16372137 G>C maps to NM_000085.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:16372137 G>C maps to NM_000085.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:16895670 C>T maps to NM_017940.3 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:16895670 C>T maps to NM_017940.3 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:35370069 C>G maps to NM_001080418.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:35370069 C>G maps to NM_001080418.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:43774765 C>T maps to NM_005424.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:43774765 C>T maps to NM_005424.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:51929377 G>A maps to NM_001981.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:51929377 G>A maps to NM_001981.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:54060428 C>A maps to NM_147193.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:54060428 C>A maps to NM_147193.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:68620904 G>A maps to NM_024911.6 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:68620904 G>A maps to NM_024911.6 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:84387004 T>G maps to NM_024686.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:84387004 T>G maps to NM_024686.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:111494890 C>A maps to NM_018372.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:111494890 C>A maps to NM_018372.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:152285219 G>T maps to NM_002016.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:152285219 G>T maps to NM_002016.1 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:152777744 A>T maps to NM_178351.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:152777744 A>T maps to NM_178351.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154018562 T>G maps to NM_207308.2 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154018562 T>G maps to NM_207308.2 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154130138 G>C maps to NM_001043351.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154130138 G>C maps to NM_001043351.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154544201 C>T maps to NM_000748.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:154544201 C>T maps to NM_000748.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:155207266 C>A maps to NM_001005742.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:155207266 C>A maps to NM_001005742.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:156845890 C>A maps to NM_002529.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:156845890 C>A maps to NM_002529.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:159273847 C>T maps to ENST00000368115 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:159273847 C>T maps to ENST00000368115 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:159897152 T>C maps to NM_001135050.1 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:159897152 T>C maps to NM_001135050.1 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:161023135 C>A maps to NM_001025598.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:161023135 C>A maps to NM_001025598.1 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:182823163 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:182823163 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:200017816 G>A maps to NM_205860.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:200017816 G>A maps to NM_205860.1 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:221879667 C>A maps to NM_007207.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:221879667 C>A maps to NM_007207.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:228471294 G>A maps to NM_001098623.1 A2943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr1:228471294 G>A maps to NM_001098623.1 A2943A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:49190072 A>G maps to NM_000145.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:49190072 A>G maps to NM_000145.3 F629F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:54093285 G>A maps to NM_014614.2 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:54093285 G>A maps to NM_014614.2 F1824F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:148705640 C>T maps to NM_181742.3 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:148705640 C>T maps to NM_181742.3 E247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:166229817 G>A maps to NM_001040142.1 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:166229817 G>A maps to NM_001040142.1 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:168108452 A>C maps to NM_152381.5 I3517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:168108452 A>C maps to NM_152381.5 I3517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:241531490 G>A maps to NM_023083.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr2:241531490 G>A maps to NM_023083.3 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:38047992 C>A maps to NM_015873.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:38047992 C>A maps to NM_015873.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:101400023 C>A maps to NM_000986.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:101400023 C>A maps to NM_000986.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:155212181 G>T maps to ENST00000340059 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:155212181 G>T maps to ENST00000340059 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:156983383 G>A maps to NM_001167912.1 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:156983383 G>A maps to NM_001167912.1 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:168845828 G>T maps to NM_004991.3 C211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr3:168845828 G>T maps to NM_004991.3 C211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:13602052 G>C maps to NM_148894.2 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:13602052 G>C maps to NM_148894.2 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:104510982 T>C maps to NM_001059.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:104510982 T>C maps to NM_001059.2 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:190862214 C>A maps to NM_004477.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr4:190862214 C>A maps to NM_004477.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:16465636 G>T maps to NM_033414.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:16465636 G>T maps to NM_033414.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:45303808 G>A maps to NM_021072.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:45303808 G>A maps to NM_021072.2 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:140517288 C>G maps to NM_015669.2 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr5:140517288 C>G maps to NM_015669.2 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:3850671 G>A maps to NM_012135.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:3850671 G>A maps to NM_012135.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:28228102 C>A maps to NM_001007531.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:28228102 C>A maps to NM_001007531.1 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:29640795 G>T maps to NM_001109809.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:29640795 G>T maps to NM_001109809.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:30128417 C>T maps to NM_006778.3 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:30128417 C>T maps to NM_006778.3 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:36291124 G>T maps to NM_001010903.4 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:36291124 G>T maps to NM_001010903.4 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:62887181 C>A maps to NM_152688.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:62887181 C>A maps to NM_152688.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:122733618 G>A maps to NM_004506.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr6:122733618 G>A maps to NM_004506.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:2284268 G>C maps to NM_198954.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:2284268 G>C maps to NM_198954.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:44880563 G>A maps to ENST00000421098 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:44880563 G>A maps to ENST00000421098 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:48280472 C>T maps to NM_152701.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr7:48280472 C>T maps to NM_152701.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:107718630 A>G maps to NM_001198533.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:107718630 A>G maps to NM_001198533.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:133941429 C>T maps to NM_003235.4 C1603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:133941429 C>T maps to NM_003235.4 C1603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:139833570 G>A maps to NM_152888.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr8:139833570 G>A maps to NM_152888.1 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:34514408 C>T maps to NM_012144.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:34514408 C>T maps to NM_012144.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:36276943 C>T maps to NM_001190388.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:36276943 C>T maps to NM_001190388.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:138379115 C>T maps to NM_014811.3 F920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr9:138379115 C>T maps to NM_014811.3 F920F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:79576343 G>T maps to NM_004747.3 V1330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:79576343 G>T maps to NM_004747.3 V1330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:82043717 C>T maps to NM_000429.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:82043717 C>T maps to NM_000429.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:127737959 G>C maps to NM_003474.4 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr10:127737959 G>C maps to NM_003474.4 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:6129719 G>T maps to NM_001005181.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:6129719 G>T maps to NM_001005181.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:6244845 G>A maps to NM_032127.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:6244845 G>A maps to NM_032127.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:60885819 T>C maps to NM_014207.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:60885819 T>C maps to NM_014207.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:68370850 G>T maps to NM_001164160.1 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:68370850 G>T maps to NM_001164160.1 E781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:119003660 C>T maps to NM_198971.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:119003660 C>T maps to NM_198971.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:128844493 A>C maps to NM_001142685.1 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr11:128844493 A>C maps to NM_001142685.1 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:1943829 G>A maps to NM_001163926.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:1943829 G>A maps to NM_001163926.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:14976351 C>G maps to NM_175874.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:14976351 C>G maps to NM_175874.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:32760949 G>T maps to NM_139241.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:32760949 G>T maps to NM_139241.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:49444318 C>A maps to NM_003482.3 E1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:49444318 C>A maps to NM_003482.3 E1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:49491847 G>A maps to NM_018113.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:49491847 G>A maps to NM_018113.2 F427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:51138368 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:51138368 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:88420328 G>T maps to NM_152589.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:88420328 G>T maps to NM_152589.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:112174761 C>T maps to NM_001136538.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:112174761 C>T maps to NM_001136538.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:112605676 G>A maps to NM_001109662.2 Q3913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:112605676 G>A maps to NM_001109662.2 Q3913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:120942705 G>C maps to NM_032314.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:120942705 G>C maps to NM_032314.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:133732755 C>T maps to NM_015394.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr12:133732755 C>T maps to NM_015394.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr13:23930095 G>A maps to NM_014363.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr13:23930095 G>A maps to NM_014363.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:71540496 C>G maps to NM_014982.2 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:71540496 C>G maps to NM_014982.2 L1696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:93944051 A>G maps to ENST00000393153 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:93944051 A>G maps to ENST00000393153 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:100375680 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:100375680 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:100792528 C>A maps to NM_207117.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:100792528 C>A maps to NM_207117.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:102904405 C>A maps to NM_014844.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr14:102904405 C>A maps to NM_014844.3 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:42041125 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:42041125 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:75305045 C>G maps to ENST00000361900 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:75305045 C>G maps to ENST00000361900 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:75305072 C>T maps to ENST00000361900 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr15:75305072 C>T maps to ENST00000361900 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:735418 G>C maps to ENST00000248142 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:735418 G>C maps to ENST00000248142 V749V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:2011250 C>T maps to NM_004548.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:2011250 C>T maps to NM_004548.2 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:3019836 G>C maps to NM_152341.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:3019836 G>C maps to NM_152341.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:19020680 C>A maps to NM_024847.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:19020680 C>A maps to NM_024847.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:77910311 G>T maps to NM_020927.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:77910311 G>T maps to NM_020927.1 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:85691123 C>T maps to NM_014615.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr16:85691123 C>T maps to NM_014615.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:7577106 A>T maps to NM_001126112.1 C277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:7577106 A>T maps to NM_001126112.1 C277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:19845218 C>T maps to NM_007202.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:19845218 C>T maps to NM_007202.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:26106003 G>T maps to NM_000625.4 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:26106003 G>T maps to NM_000625.4 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:34071980 C>T maps to NM_139285.2 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:34071980 C>T maps to NM_139285.2 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:73489626 A>G maps to ENST00000375248 T720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr17:73489626 A>G maps to ENST00000375248 T720T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A20N-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BT-A20N-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:12430205 T>C maps to NM_145276.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:12430205 T>C maps to NM_145276.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:51274694 C>T maps to NM_001506.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:51274694 C>T maps to NM_001506.1 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:54561827 G>A maps to NM_198481.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:54561827 G>A maps to NM_198481.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:57286538 G>C maps to NM_001146326.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr19:57286538 G>C maps to NM_001146326.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:10030757 C>A maps to NM_198798.1 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:10030757 C>A maps to NM_198798.1 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:32026722 C>G maps to NM_003098.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:32026722 C>G maps to NM_003098.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:41408891 G>T maps to ENST00000373198 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr20:41408891 G>T maps to ENST00000373198 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:40794948 A>G maps to NM_152505.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:40794948 A>G maps to NM_152505.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:42080496 G>A maps to NM_001389.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:42080496 G>A maps to NM_001389.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:43161780 C>T maps to ENST00000352483 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:43161780 C>T maps to ENST00000352483 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:47655202 C>A maps to NM_003906.3 L1974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr21:47655202 C>A maps to NM_003906.3 L1974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:38355471 G>T maps to ENST00000407936 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:38355471 G>T maps to ENST00000407936 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:40415272 C>T maps to NM_138435.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:40415272 C>T maps to NM_138435.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:41752422 C>T maps to ENST00000351589 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:41752422 C>T maps to ENST00000351589 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:41923344 G>C maps to ENST00000396512 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:41923344 G>C maps to ENST00000396512 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:42606217 C>A maps to NM_005650.1 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:42606217 C>A maps to NM_005650.1 S1698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:50927503 C>T maps to NM_017584.5 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chr22:50927503 C>T maps to NM_017584.5 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chrX:134033530 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chrX:134033530 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chrX:140969236 G>T maps to NM_138702.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20N-01A-11D-A14W-08 chrX:140969236 G>T maps to NM_138702.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:1669759 C>A maps to NM_182838.2 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:1669759 C>A maps to NM_182838.2 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:7724194 A>T maps to NM_015215.2 K530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:7724194 A>T maps to NM_015215.2 K530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:32673402 T>A maps to NM_001160042.1 L454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:32673402 T>A maps to NM_001160042.1 L454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:54707878 C>A maps to NM_145716.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:54707878 C>A maps to NM_145716.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:114201795 G>C maps to NM_001142782.1 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:114201795 G>C maps to NM_001142782.1 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:156563827 G>A maps to ENST00000446584 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:156563827 G>A maps to ENST00000446584 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:205902175 C>A maps to NM_134325.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:205902175 C>A maps to NM_134325.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:227227862 C>G maps to ENST00000366766 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:227227862 C>G maps to ENST00000366766 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:235972028 G>A maps to NM_000081.2 Q697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr1:235972028 G>A maps to NM_000081.2 Q697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr2:145147515 G>A maps to NM_014795.3 H1049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr2:145147515 G>A maps to NM_014795.3 H1049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr2:167141016 G>T maps to ENST00000303354 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr2:167141016 G>T maps to ENST00000303354 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:32927520 G>A maps to NM_001039111.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:32927520 G>A maps to NM_001039111.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:38318946 A>G maps to NM_004256.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:38318946 A>G maps to NM_004256.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:156234065 C>T maps to NM_172159.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr3:156234065 C>T maps to NM_172159.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:42069147 T>C maps to NM_006345.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:42069147 T>C maps to NM_006345.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:69692211 C>T maps to NM_001075.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:69692211 C>T maps to NM_001075.4 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:187541653 G>T maps to ENST00000260147 S2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr4:187541653 G>T maps to ENST00000260147 S2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:78610357 T>G maps to NM_152405.4 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:78610357 T>G maps to NM_152405.4 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:80390804 C>A maps to NM_006909.1 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:80390804 C>A maps to NM_006909.1 I583I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:127484462 C>T maps to NM_001046.2 N633N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:127484462 C>T maps to NM_001046.2 N633N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:140475831 C>G maps to NM_018936.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:140475831 C>G maps to NM_018936.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:176468220 A>T maps to ENST00000503039 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr5:176468220 A>T maps to ENST00000503039 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:12125107 C>T maps to NM_002114.2 Q1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:12125107 C>T maps to NM_002114.2 Q1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:36168657 C>T maps to NM_015695.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:36168657 C>T maps to NM_015695.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:42672297 G>A maps to NM_000322.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:42672297 G>A maps to NM_000322.4 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:56401660 C>T maps to ENST00000361203 Q5351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr6:56401660 C>T maps to ENST00000361203 Q5351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr7:36571797 G>A maps to NM_001177506.1 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr7:116166724 C>G maps to NM_001753.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr7:116166724 C>G maps to NM_001753.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr8:37732220 C>G maps to NM_001002814.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr8:37732220 C>G maps to NM_001002814.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:434791 G>A maps to NM_203447.3 K1632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:434791 G>A maps to NM_203447.3 K1632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:43625184 G>A maps to NM_001145196.1 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:43625184 G>A maps to NM_001145196.1 Q1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:100249559 C>T maps to NM_014290.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr9:100249559 C>T maps to NM_014290.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr10:12204225 G>T maps to NM_018144.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr10:12204225 G>T maps to NM_018144.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:10821760 T>C maps to ENST00000429377 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:10821760 T>C maps to ENST00000429377 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:17474773 G>A maps to ENST00000302539 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:17474773 G>A maps to ENST00000302539 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:33886305 G>T maps to NM_005574.3 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:33886305 G>T maps to NM_005574.3 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:75439096 G>A maps to NM_025098.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:75439096 G>A maps to NM_025098.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:82877724 A>C maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:82877724 A>C maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:92087449 T>G maps to ENST00000298047 Y724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:92087449 T>G maps to ENST00000298047 Y724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:93103297 G>C maps to NM_181645.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr11:93103297 G>C maps to NM_181645.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:10149500 G>A maps to NM_016509.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:10149500 G>A maps to NM_016509.3 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:12037407 C>T maps to NM_001987.4 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:12037407 C>T maps to NM_001987.4 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:51890799 C>G maps to NM_001039960.1 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:51890799 C>G maps to NM_001039960.1 V991V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:54765455 C>T maps to NM_001130967.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:54765455 C>T maps to NM_001130967.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:71977787 G>A maps to NM_003667.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:71977787 G>A maps to NM_003667.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:104336351 G>A maps to NM_003299.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:104336351 G>A maps to NM_003299.1 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:120159202 G>A maps to ENST00000392521 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:120159202 G>A maps to ENST00000392521 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:133374949 G>T maps to NM_005895.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr12:133374949 G>T maps to NM_005895.3 I638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr13:24243106 T>C maps to NM_018647.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr13:24243106 T>C maps to NM_018647.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr14:105408254 G>T maps to NM_138420.2 L4511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr14:105408254 G>T maps to NM_138420.2 L4511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr15:77472429 C>T maps to NM_024776.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr15:77472429 C>T maps to NM_024776.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:3339742 G>T maps to NM_005741.4 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:3339742 G>T maps to NM_005741.4 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:3817749 G>C maps to NM_004380.2 S1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:3817749 G>C maps to NM_004380.2 S1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:67876801 G>A maps to NM_020457.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr16:67876801 G>A maps to NM_020457.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:8273000 T>C maps to NM_213597.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:8273000 T>C maps to NM_213597.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:44076785 C>A maps to NM_001007532.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:44076785 C>A maps to NM_001007532.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:80529634 G>C maps to NM_004514.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr17:80529634 G>C maps to NM_004514.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:39037099 G>T maps to NM_000540.2 E4010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:39037099 G>T maps to NM_000540.2 E4010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:42793046 T>C maps to NM_015125.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:42793046 T>C maps to NM_015125.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:45575215 C>A maps to NM_145288.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:45575215 C>A maps to NM_145288.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:49967903 C>T maps to NM_153329.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:49967903 C>T maps to NM_153329.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:53352430 G>A maps to NM_001008801.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:53352430 G>A maps to NM_001008801.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:55776710 C>A maps to NM_012267.4 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr19:55776710 C>A maps to NM_012267.4 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr21:34648996 G>A maps to ENST00000433395 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr21:34648996 G>A maps to ENST00000433395 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr22:40415260 C>T maps to NM_138435.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chr22:40415260 C>T maps to NM_138435.2 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chrX:65486315 G>T maps to NM_138737.3 V1147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20O-01A-21D-A14W-08 chrX:65486315 G>T maps to NM_138737.3 V1147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:11561645 G>C maps to NM_020780.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:11561645 G>C maps to NM_020780.1 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:38197143 C>T maps to NM_001099439.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:38197143 C>T maps to NM_001099439.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:45101241 G>A maps to ENST00000453887 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:45101241 G>A maps to ENST00000453887 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:159021524 G>A maps to ENST00000295809 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:159021524 G>A maps to ENST00000295809 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:173454532 G>T maps to NM_004905.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:173454532 G>T maps to NM_004905.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:200967638 G>A maps to NM_017596.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:200967638 G>A maps to NM_017596.2 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:220162080 G>A maps to NM_004446.2 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr1:220162080 G>A maps to NM_004446.2 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr2:71748030 G>A maps to NM_001130987.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr2:71748030 G>A maps to NM_001130987.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr2:233345139 G>A maps to NM_004826.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr2:233345139 G>A maps to NM_004826.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr3:49929004 C>A maps to NM_002447.2 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr3:49929004 C>A maps to NM_002447.2 E1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr3:184295483 C>T maps to NM_004443.3 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr3:184295483 C>T maps to NM_004443.3 N506N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr4:77230915 C>T maps to NM_003943.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr4:77230915 C>T maps to NM_003943.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr6:29913230 G>T maps to ENST00000376806 *372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr6:29913230 G>T maps to ENST00000376806 *372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr7:90895307 C>T maps to NM_003505.1 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr7:90895307 C>T maps to NM_003505.1 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr7:111379264 G>T maps to ENST00000428084 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr7:111379264 G>T maps to ENST00000428084 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:20414339 G>A maps to NM_004529.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:20414339 G>A maps to NM_004529.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:38396623 C>T maps to NM_000692.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:38396623 C>T maps to NM_000692.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:120475701 C>T maps to NM_138554.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:120475701 C>T maps to NM_138554.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:133499064 G>T maps to NM_003934.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:133499064 G>T maps to NM_003934.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:135781357 A>T maps to NM_000368.4 L536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr9:135781357 A>T maps to NM_000368.4 L536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr10:78799314 G>A maps to NM_001161352.1 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr10:78799314 G>A maps to NM_001161352.1 F610F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr10:93751912 C>A maps to NM_003972.2 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr10:93751912 C>A maps to NM_003972.2 V964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr11:10821250 C>G maps to ENST00000429377 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr11:10821250 C>G maps to ENST00000429377 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr11:64884084 G>T maps to NM_014205.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr11:64884084 G>T maps to NM_014205.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:8926378 G>C maps to NM_020734.2 *387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:8926378 G>C maps to NM_020734.2 *387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:15035936 G>A maps to NM_001190839.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:15035936 G>A maps to NM_001190839.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:56088079 G>A maps to ENST00000347027 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:56088079 G>A maps to ENST00000347027 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:122999746 C>T maps to NM_023012.5 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr12:122999746 C>T maps to NM_023012.5 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr15:75942366 G>C maps to NM_153271.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr15:75942366 G>C maps to NM_153271.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr16:11114143 C>T maps to ENST00000409790 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr16:11114143 C>T maps to ENST00000409790 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr16:89869699 C>G maps to NM_000135.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr16:89869699 C>G maps to NM_000135.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:10430321 G>C maps to NM_017534.5 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:10430321 G>C maps to NM_017534.5 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:18082088 G>T maps to ENST00000205890 E3500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:18082088 G>T maps to ENST00000205890 E3500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:42855098 G>C maps to NM_002390.4 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:42855098 G>C maps to NM_002390.4 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:47284178 G>C maps to NM_001198754.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:47284178 G>C maps to NM_001198754.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:48940622 T>C maps to NM_005749.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr17:48940622 T>C maps to NM_005749.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr19:34791437 C>T maps to NM_014686.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr19:34791437 C>T maps to NM_014686.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr20:61428555 G>C maps to NM_018270.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr20:61428555 G>C maps to NM_018270.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr22:18171755 C>T maps to NM_015367.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chr22:18171755 C>T maps to NM_015367.2 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chrX:8995956 C>T maps to NM_205849.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chrX:8995956 C>T maps to NM_205849.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chrX:54259292 G>A maps to NM_020922.4 R1597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20P-01A-11D-A14W-08 chrX:54259292 G>A maps to NM_020922.4 R1597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:16918402 G>C maps to NM_017940.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:16918402 G>C maps to NM_017940.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:19441917 C>T maps to ENST00000375267 E3679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:19441917 C>T maps to ENST00000375267 E3679E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:100920980 C>T maps to NM_033312.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:100920980 C>T maps to NM_033312.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:116670902 G>A maps to NM_152367.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:116670902 G>A maps to NM_152367.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:155168290 C>A maps to NM_007112.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:155168290 C>A maps to NM_007112.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:156503867 G>C maps to NM_178229.4 S1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:156503867 G>C maps to NM_178229.4 S1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:173176221 G>A maps to NM_003326.3 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:173176221 G>A maps to NM_003326.3 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:201060840 G>C maps to NM_000069.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:201060840 G>C maps to NM_000069.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:202124737 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:202124737 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:227071518 G>A maps to ENST00000391872 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr1:227071518 G>A maps to ENST00000391872 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr2:85785669 C>T maps to NM_000821.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr2:85785669 C>T maps to NM_000821.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:49249259 C>A maps to NM_178173.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:49249259 C>A maps to NM_178173.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:49723525 G>T maps to NM_020998.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:49723525 G>T maps to NM_020998.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:93761857 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:93761857 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:184557484 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr3:184557484 G>A did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:106156624 C>G maps to ENST00000513237 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:106156624 C>G maps to ENST00000513237 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:160253616 C>T maps to NM_014247.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:160253616 C>T maps to NM_014247.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:166414358 C>T maps to NM_001873.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr4:166414358 C>T maps to NM_001873.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr5:36985879 A>G maps to NM_133433.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr5:36985879 A>G maps to NM_133433.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr5:140209469 C>T maps to NM_018909.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr5:140209469 C>T maps to NM_018909.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr6:32148013 C>T maps to NM_006913.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr6:32148013 C>T maps to NM_006913.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:30721546 G>C maps to ENST00000348438 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:30721546 G>C maps to ENST00000348438 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:56022648 G>A maps to ENST00000426595 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:56022648 G>A maps to ENST00000426595 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:139636072 G>A maps to NM_001166253.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr7:139636072 G>A maps to NM_001166253.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr9:96320267 C>T maps to ENST00000333936 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr9:96320267 C>T maps to ENST00000333936 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr10:23321934 C>T maps to NM_173081.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr10:23321934 C>T maps to NM_173081.3 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr10:135350732 C>T maps to NM_000773.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr10:135350732 C>T maps to NM_000773.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr12:44124322 T>C maps to NM_031292.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr12:44124322 T>C maps to NM_031292.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr15:64446589 G>C maps to NM_024798.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr15:64446589 G>C maps to NM_024798.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:2510686 C>T maps to NM_025108.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:2510686 C>T maps to NM_025108.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:12758793 C>G maps to NM_018340.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:12758793 C>G maps to NM_018340.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:72110370 C>G maps to ENST00000228226 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr16:72110370 C>G maps to ENST00000228226 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:16022772 G>A maps to ENST00000395857 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:16022772 G>A maps to ENST00000395857 R627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:25936220 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:25936220 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:44109506 G>C maps to NM_015443.3 S999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr17:44109506 G>C maps to NM_015443.3 S999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr18:51818252 C>T maps to NM_007195.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr18:51818252 C>T maps to NM_007195.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr18:74091603 G>A maps to ENST00000443185 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr18:74091603 G>A maps to ENST00000443185 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:8046038 G>A maps to ENST00000351593 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:8046038 G>A maps to ENST00000351593 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:19737748 G>A maps to NM_004720.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:19737748 G>A maps to NM_004720.5 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:38229522 G>C maps to NM_001172690.1 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:38229522 G>C maps to NM_001172690.1 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:49713573 C>T maps to NM_017636.3 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:49713573 C>T maps to NM_017636.3 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:54967250 T>G maps to ENST00000431846 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr19:54967250 T>G maps to ENST00000431846 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr20:16719530 C>G maps to NM_198220.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr20:16719530 C>G maps to NM_198220.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr21:40604197 G>A maps to NM_018963.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr21:40604197 G>A maps to NM_018963.3 R969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr22:23465560 C>T maps to NM_002073.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr22:23465560 C>T maps to NM_002073.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr22:41739423 C>A maps to ENST00000351589 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chr22:41739423 C>A maps to ENST00000351589 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chrX:153049815 C>T maps to NM_014370.3 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20Q-01A-11D-A14W-08 chrX:153049815 C>T maps to NM_014370.3 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:957837 G>A maps to NM_198576.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:957837 G>A maps to NM_198576.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:3800259 C>T maps to ENST00000430539 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:3800259 C>T maps to ENST00000430539 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:65145287 G>A maps to ENST00000371073 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:65145287 G>A maps to ENST00000371073 V1085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:70488896 G>A maps to NM_020794.2 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:70488896 G>A maps to NM_020794.2 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:78045313 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:78045313 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:117633210 G>T maps to NM_003594.3 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:117633210 G>T maps to NM_003594.3 E852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:150443791 C>T maps to NM_015203.3 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:150443791 C>T maps to NM_015203.3 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:167381394 G>A maps to NM_002697.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:167381394 G>A maps to NM_002697.3 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:176903363 C>T maps to ENST00000281881 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:176903363 C>T maps to ENST00000281881 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:247464252 G>A maps to NM_032752.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr1:247464252 G>A maps to NM_032752.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:25994387 G>T maps to NM_018263.4 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:25994387 G>T maps to NM_018263.4 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:27501156 G>A maps to NM_173650.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:27501156 G>A maps to NM_173650.1 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:43458381 G>C maps to ENST00000330266 S1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:43458381 G>C maps to ENST00000330266 S1857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:74686772 C>T maps to ENST00000452361 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:74686772 C>T maps to ENST00000452361 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:101580598 C>T maps to NM_002518.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:101580598 C>T maps to NM_002518.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:179584462 G>C maps to NM_133378.4 S6675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:179584462 G>C maps to NM_133378.4 S6675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:198498721 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:198498721 C>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:242066100 G>C maps to ENST00000358649 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr2:242066100 G>C maps to ENST00000358649 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:15124020 G>T maps to NM_022340.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:15124020 G>T maps to NM_022340.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:31710300 C>T maps to NM_017784.4 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:31710300 C>T maps to NM_017784.4 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:49043564 C>G maps to NM_177938.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:49043564 C>G maps to NM_177938.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:49161497 G>A maps to NM_002292.3 Q1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:49161497 G>A maps to NM_002292.3 Q1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:57827094 C>G maps to ENST00000428312 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:57827094 C>G maps to ENST00000428312 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:113673210 C>A maps to NM_173570.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:113673210 C>A maps to NM_173570.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:124738227 G>C maps to NM_020733.1 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:124738227 G>C maps to NM_020733.1 S489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:128753033 C>T maps to NM_024768.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:128753033 C>T maps to NM_024768.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:129023616 G>A maps to NM_001006109.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:129023616 G>A maps to NM_001006109.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:130688228 C>A maps to NM_001001486.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:130688228 C>A maps to NM_001001486.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:184009860 G>T maps to NM_014693.3 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:184009860 G>T maps to NM_014693.3 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:197408131 C>T maps to NM_014687.1 W766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr3:197408131 C>T maps to NM_014687.1 W766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:1957528 G>A maps to NM_133335.3 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:1957528 G>A maps to NM_133335.3 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:26959235 C>T maps to ENST00000382009 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:26959235 C>T maps to ENST00000382009 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:66230765 G>A maps to NM_004439.5 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:66230765 G>A maps to NM_004439.5 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:189026056 C>G maps to ENST00000326754 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr4:189026056 C>G maps to ENST00000326754 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:43295897 C>T maps to NM_002130.6 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:43295897 C>T maps to NM_002130.6 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140256019 C>T maps to NM_018903.2 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140256019 C>T maps to NM_018903.2 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140476447 C>T maps to NM_018936.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140476447 C>T maps to NM_018936.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140482300 C>T maps to NM_018937.2 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140482300 C>T maps to NM_018937.2 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140567182 C>T maps to NM_019119.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140567182 C>T maps to NM_019119.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140736302 G>A maps to NM_018917.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:140736302 G>A maps to NM_018917.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:147715196 C>G maps to NM_001040433.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:147715196 C>G maps to NM_001040433.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:171327030 C>A maps to NM_012300.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:171327030 C>A maps to NM_012300.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:12164681 G>A maps to NM_002114.2 V2715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:12164681 G>A maps to NM_002114.2 V2715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:27775561 G>C maps to NM_003519.3 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:27775561 G>C maps to NM_003519.3 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:28327554 G>A maps to NM_024493.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:28327554 G>A maps to NM_024493.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:41051849 C>A maps to NM_002505.4 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:41051849 C>A maps to NM_002505.4 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:43194089 G>A maps to ENST00000509253 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:43194089 G>A maps to ENST00000509253 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:89974214 G>A maps to NM_002043.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:89974214 G>A maps to NM_002043.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:106553145 C>A maps to NM_001198.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:106553145 C>A maps to NM_001198.3 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:150387241 G>A maps to NM_024518.1 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr6:150387241 G>A maps to NM_024518.1 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:44739834 A>G maps to ENST00000444676 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:44739834 A>G maps to ENST00000444676 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:124475364 T>A maps to NM_015450.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:124475364 T>A maps to NM_015450.2 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:148769088 G>A maps to NM_152411.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:148769088 G>A maps to NM_152411.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:154561136 G>A maps to NM_130797.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr7:154561136 G>A maps to NM_130797.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:24178762 C>T maps to NM_014265.4 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:24178762 C>T maps to NM_014265.4 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:33346597 G>A maps to NM_032509.3 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:33346597 G>A maps to NM_032509.3 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:38271716 C>T maps to NM_001174067.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:38271716 C>T maps to NM_001174067.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:49643171 G>T maps to NM_024593.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:49643171 G>T maps to NM_024593.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:69046487 C>T maps to NM_024870.2 Q1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:69046487 C>T maps to NM_024870.2 Q1321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:101153668 T>C maps to NM_001029860.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:101153668 T>C maps to NM_001029860.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:109228655 C>T maps to NM_001568.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr8:109228655 C>T maps to NM_001568.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:73233872 G>A maps to ENST00000419692 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:73233872 G>A maps to ENST00000419692 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:95274342 G>A maps to NM_001393.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:95274342 G>A maps to NM_001393.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:139945380 G>C maps to NM_203468.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:139945380 G>C maps to NM_203468.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:139945963 G>A maps to NM_203468.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr9:139945963 G>A maps to NM_203468.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr10:91099495 C>T maps to NM_001549.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr10:91099495 C>T maps to NM_001549.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr10:126505168 C>G maps to NM_032182.3 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr10:126505168 C>G maps to NM_032182.3 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:14825540 G>A maps to NM_000922.3 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:14825540 G>A maps to NM_000922.3 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:18586471 G>A maps to NM_001040697.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:18586471 G>A maps to NM_001040697.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:57958522 C>G maps to NM_001005283.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:57958522 C>G maps to NM_001005283.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:58189809 G>A maps to NM_001005566.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:58189809 G>A maps to NM_001005566.2 L309L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A20T-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:66030505 C>A maps to NM_022822.2 R251R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A20T-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:66030505 C>A maps to NM_022822.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:66082599 G>A maps to NM_020404.2 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:66082599 G>A maps to NM_020404.2 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:71719866 G>A maps to ENST00000393695 R1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:71719866 G>A maps to ENST00000393695 R1701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:71728851 G>A maps to ENST00000393695 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:71728851 G>A maps to ENST00000393695 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:118529681 G>A maps to ENST00000264029 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:118529681 G>A maps to ENST00000264029 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:126138750 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr11:126138750 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:69207365 A>G maps to NM_002392.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:69207365 A>G maps to NM_002392.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:86199358 G>A maps to NM_005447.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:86199358 G>A maps to NM_005447.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:95918478 G>C maps to NM_032147.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:95918478 G>C maps to NM_032147.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:108008936 C>T maps to NM_001018072.1 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:108008936 C>T maps to NM_001018072.1 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:132547086 G>A maps to ENST00000333577 Q2761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr12:132547086 G>A maps to ENST00000333577 Q2761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:95726578 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:95726578 C>T did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:113730362 T>A maps to NM_001112732.1 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:113730362 T>A maps to NM_001112732.1 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:115008756 C>T maps to NM_003903.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr13:115008756 C>T maps to NM_003903.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:21025033 G>A maps to NM_001110361.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:21025033 G>A maps to NM_001110361.1 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:21556226 C>T maps to NM_018071.3 A1496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:21556226 C>T maps to NM_018071.3 A1496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:94088399 G>A maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr14:94088399 G>A maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr15:89379445 T>A maps to NM_013227.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr15:89379445 T>A maps to NM_013227.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:726496 G>A maps to NM_003961.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:726496 G>A maps to NM_003961.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:3820791 G>A maps to NM_004380.2 Q887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:3820791 G>A maps to NM_004380.2 Q887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:3820951 G>C maps to NM_004380.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:3820951 G>C maps to NM_004380.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:4862197 G>A maps to NM_032569.3 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:4862197 G>A maps to NM_032569.3 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:30092609 G>A maps to NM_002720.1 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:30092609 G>A maps to NM_002720.1 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:47347637 A>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:47347637 A>G did not map to a codon.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:54319258 G>A maps to NM_024336.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:54319258 G>A maps to NM_024336.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:71805128 G>A maps to ENST00000423132 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr16:71805128 G>A maps to ENST00000423132 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:7217457 G>T maps to NM_004489.4 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:7217457 G>T maps to NM_004489.4 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:62865277 G>C maps to NM_199340.2 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:62865277 G>C maps to NM_199340.2 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:67270111 G>A maps to ENST00000392677 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr17:67270111 G>A maps to ENST00000392677 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr18:670746 G>A maps to NM_001071.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr18:670746 G>A maps to NM_001071.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr18:33607164 G>A maps to NM_018170.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr18:33607164 G>A maps to NM_018170.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:1818819 G>A maps to NM_020695.3 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:1818819 G>A maps to NM_020695.3 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:8999518 G>C maps to NM_024690.2 T13552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:8999518 G>C maps to NM_024690.2 T13552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:36728008 C>T maps to NM_007145.2 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:36728008 C>T maps to NM_007145.2 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:43575861 G>C maps to NM_031246.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:43575861 G>C maps to NM_031246.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:44514436 G>A maps to NM_006300.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:44514436 G>A maps to NM_006300.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:46275903 C>A maps to NM_004409.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:46275903 C>A maps to NM_004409.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:46973830 C>A maps to NM_018215.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:46973830 C>A maps to NM_018215.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:55494634 G>A maps to NM_017852.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr19:55494634 G>A maps to NM_017852.3 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr20:46265060 C>G maps to NM_181659.2 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr20:46265060 C>G maps to NM_181659.2 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr21:38444857 C>T maps to NM_153681.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr21:38444857 C>T maps to NM_153681.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:23482514 C>T maps to NM_014433.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:23482514 C>T maps to NM_014433.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:36960928 C>T maps to NM_006078.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:36960928 C>T maps to NM_006078.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:39708980 C>T maps to NM_000967.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:39708980 C>T maps to NM_000967.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43089309 G>A maps to NM_017436.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43089309 G>A maps to NM_017436.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43520162 C>T maps to NM_001197.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43520162 C>T maps to NM_001197.3 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43972200 C>T maps to NM_022785.3 Q1132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:43972200 C>T maps to NM_022785.3 Q1132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:46725394 G>C maps to NM_016426.6 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr22:46725394 G>C maps to NM_016426.6 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chrX:132161711 C>T maps to NM_031907.1 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chrX:132161711 C>T maps to NM_031907.1 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:1203255 C>T maps to NM_194315.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:1203255 C>T maps to NM_194315.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:3703762 C>A maps to NM_020710.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:3703762 C>A maps to NM_020710.2 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:46763282 C>T maps to ENST00000254454 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:46763282 C>T maps to ENST00000254454 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:82451024 C>G maps to ENST00000370717 S1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:82451024 C>G maps to ENST00000370717 S1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:155252453 C>T maps to NM_020897.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:155252453 C>T maps to NM_020897.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:245809540 C>T maps to NM_018012.3 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr1:245809540 C>T maps to NM_018012.3 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:9483387 C>T maps to ENST00000407969 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:9483387 C>T maps to ENST00000407969 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:49064435 G>T maps to NM_000884.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:49064435 G>T maps to NM_000884.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:119451309 C>G maps to NM_033364.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:119451309 C>G maps to NM_033364.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:141889248 G>A maps to NM_001039547.2 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr3:141889248 G>A maps to NM_001039547.2 D453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr4:187549508 G>A maps to ENST00000260147 Q1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr4:187549508 G>A maps to ENST00000260147 Q1537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr4:187549806 G>T maps to ENST00000260147 I1478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr4:187549806 G>T maps to ENST00000260147 I1478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr6:26452380 C>T maps to NM_006994.4 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr6:26452380 C>T maps to NM_006994.4 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr6:136599222 G>A maps to NM_014739.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr6:136599222 G>A maps to NM_014739.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr7:77010666 A>G maps to NM_017439.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr7:77010666 A>G maps to NM_017439.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:32098164 G>A maps to NM_018287.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:32098164 G>A maps to NM_018287.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:62553723 G>A maps to NM_001786.4 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:62553723 G>A maps to NM_001786.4 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:63170340 G>A maps to NM_178505.6 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr10:63170340 G>A maps to NM_178505.6 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:3716746 G>A maps to NM_016320.4 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:3716746 G>A maps to NM_016320.4 Q1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:62393545 G>A maps to NM_198335.2 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:62393545 G>A maps to NM_198335.2 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:62393546 G>A maps to NM_198335.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:62393546 G>A maps to NM_198335.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:76175123 G>A maps to ENST00000393457 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr11:76175123 G>A maps to ENST00000393457 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr12:123340549 G>A maps to NM_003959.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr12:123340549 G>A maps to NM_003959.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr14:73743888 G>C maps to NM_001005743.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr14:73743888 G>C maps to NM_001005743.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr15:55839114 G>T maps to NM_015617.1 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr15:55839114 G>T maps to NM_015617.1 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:1841119 C>T maps to NM_001146006.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:1841119 C>T maps to NM_001146006.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:46650006 G>A maps to NM_024745.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:46650006 G>A maps to NM_024745.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:89788954 C>T maps to NM_001113525.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr16:89788954 C>T maps to NM_001113525.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr17:42225569 C>T maps to NM_024032.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr17:42225569 C>T maps to NM_024032.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr17:78936368 G>C maps to NM_020761.2 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr17:78936368 G>C maps to NM_020761.2 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr20:13098329 C>T maps to NM_018327.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr20:13098329 C>T maps to NM_018327.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr20:62657329 G>A maps to NM_012469.3 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chr20:62657329 G>A maps to NM_012469.3 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chrX:73962898 G>C maps to NM_001008537.2 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20U-01A-11D-A14W-08 chrX:73962898 G>C maps to NM_001008537.2 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:8395588 C>G maps to ENST00000377479 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:8395588 C>G maps to ENST00000377479 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:16907360 G>A maps to NM_017940.3 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:16907360 G>A maps to NM_017940.3 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:78958973 G>A maps to NM_000959.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:78958973 G>A maps to NM_000959.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:175105996 G>A maps to NM_022093.1 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr1:175105996 G>A maps to NM_022093.1 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:43801787 A>G maps to ENST00000330266 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:43801787 A>G maps to ENST00000330266 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:61315571 C>T maps to NM_001129993.1 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:61315571 C>T maps to NM_001129993.1 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:136587247 T>C did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr2:136587247 T>C did not map to a codon.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:49152978 G>A maps to ENST00000434032 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:49152978 G>A maps to ENST00000434032 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:52491870 C>T maps to NM_007184.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:52491870 C>T maps to NM_007184.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:132360901 C>A maps to NM_032169.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr3:132360901 C>A maps to NM_032169.4 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr5:16672862 G>A maps to NM_012334.2 N1748N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr5:16672862 G>A maps to NM_012334.2 N1748N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr5:98228328 G>A maps to NM_001270.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr5:98228328 G>A maps to NM_001270.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:152639224 C>T maps to NM_182961.2 K5521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:152639224 C>T maps to NM_182961.2 K5521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:152749509 C>A maps to NM_182961.2 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:152749509 C>A maps to NM_182961.2 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:160221822 G>C maps to NM_173516.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr6:160221822 G>C maps to NM_173516.1 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr7:1594928 C>T maps to NM_001097620.1 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr7:1594928 C>T maps to NM_001097620.1 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr7:77762249 C>T maps to NM_012301.3 Q1053Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr7:77762249 C>T maps to NM_012301.3 Q1053Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr8:24771629 G>A maps to NM_005382.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr8:24771629 G>A maps to NM_005382.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr9:20414345 G>A maps to NM_004529.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr9:20414345 G>A maps to NM_004529.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:17083211 C>T maps to NM_001081.3 E1279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:17083211 C>T maps to NM_001081.3 E1279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:26492007 C>T maps to NM_017433.4 Q1568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:26492007 C>T maps to NM_017433.4 Q1568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:122334733 C>G maps to NM_001030059.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr10:122334733 C>G maps to NM_001030059.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:609397 G>A maps to ENST00000264555 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:609397 G>A maps to ENST00000264555 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:19252337 C>G maps to NM_024680.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:19252337 C>G maps to NM_024680.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr12:53722481 G>A maps to NM_001173467.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr12:53722481 G>A maps to NM_001173467.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:2806514 G>A maps to NM_016333.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:2806514 G>A maps to NM_016333.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:30376494 G>A maps to NM_015527.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:30376494 G>A maps to NM_015527.3 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:31122037 T>C maps to NM_005881.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:31122037 T>C maps to NM_005881.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:46694416 G>A maps to NM_018206.4 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr16:46694416 G>A maps to NM_018206.4 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:33444637 G>A maps to NM_032816.3 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:33444637 G>A maps to NM_032816.3 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:50370413 A>G maps to NM_007254.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr19:50370413 A>G maps to NM_007254.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr20:32378875 G>A maps to ENST00000375200 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr20:32378875 G>A maps to ENST00000375200 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr21:41447092 G>A maps to NM_001389.3 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chr21:41447092 G>A maps to NM_001389.3 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chrX:3030587 G>A maps to NM_004042.3 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chrX:3030587 G>A maps to NM_004042.3 E588E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chrX:70340914 T>G maps to ENST00000333646 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chrX:70340914 T>G maps to ENST00000333646 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chrX:153035385 C>T maps to NM_005393.2 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20V-01A-11D-A14W-08 chrX:153035385 C>T maps to NM_005393.2 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr1:67666417 A>C did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr1:67666417 A>C did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr1:161276711 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr1:161276711 C>A did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:20647510 C>T maps to NM_004040.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:20647510 C>T maps to NM_004040.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:220147643 G>A maps to NM_006736.5 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:220147643 G>A maps to NM_006736.5 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:235405158 G>A maps to ENST00000339728 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr2:235405158 G>A maps to ENST00000339728 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr3:78685191 G>C maps to NM_002941.3 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr3:78685191 G>C maps to NM_002941.3 S1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr5:140741600 C>T maps to NM_018923.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr5:140741600 C>T maps to NM_018923.2 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr5:180057287 C>T maps to NM_182925.4 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr5:180057287 C>T maps to NM_182925.4 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr6:108193030 C>T maps to NM_007214.4 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr6:108193030 C>T maps to NM_007214.4 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr6:163984653 C>T maps to ENST00000361752 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr6:163984653 C>T maps to ENST00000361752 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:43508601 C>G maps to NM_015052.3 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:43508601 C>G maps to NM_015052.3 R999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:129908840 A>G maps to NM_001869.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:129908840 A>G maps to NM_001869.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr8:8185378 G>A maps to NM_001080826.1 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr8:8185378 G>A maps to NM_001080826.1 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr8:135615034 G>T maps to NM_020863.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr8:135615034 G>T maps to NM_020863.3 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:100692794 T>G maps to NM_018437.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:100692794 T>G maps to NM_018437.3 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:104314696 G>A maps to NM_019592.5 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:104314696 G>A maps to NM_019592.5 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:135276960 G>A maps to NM_007344.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr9:135276960 G>A maps to NM_007344.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr10:72292375 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr10:72292375 G>T did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:3877559 C>G maps to NM_003156.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:3877559 C>G maps to NM_003156.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:7642182 C>T maps to NM_003621.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:7642182 C>T maps to NM_003621.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:109294574 C>T maps to NM_207645.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr11:109294574 C>T maps to NM_207645.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr12:5020705 C>A maps to NM_000217.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr12:5020705 C>A maps to NM_000217.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr12:22015989 T>A did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr12:22015989 T>A did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr13:36744905 G>C maps to ENST00000511166 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr13:36744905 G>C maps to ENST00000511166 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr13:75936293 G>A maps to ENST00000431480 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr13:75936293 G>A maps to ENST00000431480 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr16:2052219 C>T maps to ENST00000431526 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr16:2052219 C>T maps to ENST00000431526 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr17:7226378 C>A maps to NM_032442.2 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr17:7226378 C>A maps to NM_032442.2 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr17:40642596 T>G maps to NM_001130020.1 Y379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr17:40642596 T>G maps to NM_001130020.1 Y379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:9085812 G>C maps to NM_024690.2 S2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:9085812 G>C maps to NM_024690.2 S2001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:39086327 C>A maps to NM_001042600.1 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:39086327 C>A maps to NM_001042600.1 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:39516068 C>G maps to NM_178820.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:39516068 C>G maps to NM_178820.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:56467115 C>T maps to NM_176811.2 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr19:56467115 C>T maps to NM_176811.2 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr21:30699116 T>G maps to NM_206866.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr21:30699116 T>G maps to NM_206866.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr22:31816284 G>A maps to NM_004147.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr22:31816284 G>A maps to NM_004147.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chrX:67940174 A>C maps to NM_001142503.2 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chrX:67940174 A>C maps to NM_001142503.2 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chrX:115573894 A>G maps to NM_007231.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chrX:115573894 A>G maps to NM_007231.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:1455590 G>A maps to NM_018188.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:1455590 G>A maps to NM_018188.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:6206805 C>T maps to NM_015557.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:6206805 C>T maps to NM_015557.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:16256133 T>C maps to NM_015001.2 Y1133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:16256133 T>C maps to NM_015001.2 Y1133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:21031303 C>T maps to NM_020816.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:21031303 C>T maps to NM_020816.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:23637375 G>A maps to ENST00000414299 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:23637375 G>A maps to ENST00000414299 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:39878174 G>A maps to NM_015038.1 Q746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:39878174 G>A maps to NM_015038.1 Q746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:53546443 G>T maps to NM_153703.4 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:53546443 G>T maps to NM_153703.4 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:86123572 C>T maps to NM_017953.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:86123572 C>T maps to NM_017953.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:153958589 G>A maps to NM_002870.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:153958589 G>A maps to NM_002870.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:161140555 C>T maps to NM_001122764.1 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:161140555 C>T maps to NM_001122764.1 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:181767564 G>A maps to ENST00000357570 A2179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:181767564 G>A maps to ENST00000357570 A2179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:202705487 G>C maps to ENST00000367264 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:202705487 G>C maps to ENST00000367264 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:203134832 C>A maps to NM_001048230.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:203134832 C>A maps to NM_001048230.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:205492698 C>T maps to NM_212503.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:205492698 C>T maps to NM_212503.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:235377118 G>A maps to NM_016374.5 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr1:235377118 G>A maps to NM_016374.5 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:33614356 C>T maps to ENST00000354476 P1607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:33614356 C>T maps to ENST00000354476 P1607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:131904339 C>T maps to ENST00000409158 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:131904339 C>T maps to ENST00000409158 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:189950443 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:189950443 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:197080608 C>A maps to NM_020760.1 G1529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:197080608 C>A maps to NM_020760.1 G1529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:220344838 C>T maps to NM_005876.4 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:220344838 C>T maps to NM_005876.4 P1773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:241420352 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr2:241420352 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr3:109031404 C>T maps to NM_138815.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr3:109031404 C>T maps to NM_138815.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr3:122277248 C>T maps to NM_031458.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr3:122277248 C>T maps to NM_031458.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:5966858 G>A maps to ENST00000324058 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:5966858 G>A maps to ENST00000324058 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:66467437 G>A maps to NM_004439.5 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:66467437 G>A maps to NM_004439.5 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:123171628 C>T maps to NM_015312.3 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:123171628 C>T maps to NM_015312.3 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:126336817 C>T maps to NM_024582.4 R2234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr4:126336817 C>T maps to NM_024582.4 R2234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:1221322 C>T maps to NM_001003841.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:1221322 C>T maps to NM_001003841.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:13737393 G>A maps to NM_001369.2 Q3808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:13737393 G>A maps to NM_001369.2 Q3808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:15936773 C>T maps to NM_012304.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:15936773 C>T maps to NM_012304.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:56177955 C>T maps to NM_005921.1 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:56177955 C>T maps to NM_005921.1 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:161119110 C>T maps to NM_000811.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr5:161119110 C>T maps to NM_000811.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:32095972 C>G maps to NM_004381.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:32095972 C>G maps to NM_004381.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:32947662 G>T maps to ENST00000395289 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:32947662 G>T maps to ENST00000395289 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:170594689 G>A maps to NM_005618.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr6:170594689 G>A maps to NM_005618.3 Q277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:7278180 G>A maps to NM_020156.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:7278180 G>A maps to NM_020156.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:37901703 T>C maps to NM_016616.4 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:37901703 T>C maps to NM_016616.4 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:66479464 C>T maps to NM_018264.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:66479464 C>T maps to NM_018264.2 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:72865288 G>A maps to NM_032408.3 I1156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:72865288 G>A maps to NM_032408.3 I1156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:150696093 C>T maps to NM_000603.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr7:150696093 C>T maps to NM_000603.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr8:23429028 C>T maps to NM_016612.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr8:23429028 C>T maps to NM_016612.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr8:101078405 G>T maps to NM_015668.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr8:101078405 G>T maps to NM_015668.3 S238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:73002700 G>A maps to NM_001206.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:73002700 G>A maps to NM_001206.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:116812344 G>A maps to ENST00000374126 G921G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:116812344 G>A maps to ENST00000374126 G921G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:129854111 G>A maps to NM_012098.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:129854111 G>A maps to NM_012098.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:136402525 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr9:136402525 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:38121958 G>A maps to NM_021045.1 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:38121958 G>A maps to NM_021045.1 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:95157002 C>T maps to ENST00000371489 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:95157002 C>T maps to ENST00000371489 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:115609944 C>A maps to NM_014881.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr10:115609944 C>A maps to NM_014881.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:4626602 C>T maps to NM_018073.5 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:4626602 C>T maps to NM_018073.5 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:5443928 C>T maps to NM_001004757.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:5443928 C>T maps to NM_001004757.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:6661248 C>A maps to NM_003737.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:6661248 C>A maps to NM_003737.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:34182491 G>A maps to NM_145804.2 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:34182491 G>A maps to NM_145804.2 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:57982647 T>C maps to NM_001004458.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:57982647 T>C maps to NM_001004458.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:59132284 C>T maps to NM_001004729.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:59132284 C>T maps to NM_001004729.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:128857988 G>A maps to NM_001142685.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr11:128857988 G>A maps to NM_001142685.1 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:9259152 G>A maps to NM_000014.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:9259152 G>A maps to NM_000014.4 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:11506382 C>T maps to NM_005039.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:11506382 C>T maps to NM_005039.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:55820918 G>A maps to NM_001005183.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:55820918 G>A maps to NM_001005183.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:56355230 G>A maps to NM_006928.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:56355230 G>A maps to NM_006928.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:57603646 C>T maps to NM_002332.2 P4145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:57603646 C>T maps to NM_002332.2 P4145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:104698236 C>T maps to NM_001008394.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:104698236 C>T maps to NM_001008394.1 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:117610322 G>C maps to NM_033624.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:117610322 G>C maps to NM_033624.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:132490705 C>G maps to ENST00000333577 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr12:132490705 C>G maps to ENST00000333577 L1031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:29236559 C>T maps to NM_005249.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:29236559 C>T maps to NM_005249.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:42361124 C>T maps to NM_152447.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:42361124 C>T maps to NM_152447.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:94155066 C>G maps to ENST00000393153 L2383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr14:94155066 C>G maps to ENST00000393153 L2383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:735980 C>A maps to ENST00000248142 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:735980 C>A maps to ENST00000248142 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:2012181 G>A maps to NM_002952.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:2012181 G>A maps to NM_002952.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:3142560 G>A maps to NM_032805.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:3142560 G>A maps to NM_032805.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:24990326 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:24990326 C>T did not map to a codon.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:30734384 C>A maps to NM_006662.2 R1332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:30734384 C>A maps to NM_006662.2 R1332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:84118641 G>C maps to NM_003791.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr16:84118641 G>C maps to NM_003791.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:10600713 C>G maps to NM_004589.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:10600713 C>G maps to NM_004589.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:27233883 C>T maps to NM_001033561.1 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:27233883 C>T maps to NM_001033561.1 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:36482905 G>A maps to ENST00000398597 V2183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:36482905 G>A maps to ENST00000398597 V2183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:56395742 G>A maps to NM_004758.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:56395742 G>A maps to NM_004758.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:71391323 G>A maps to NM_001144952.1 Q1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr17:71391323 G>A maps to NM_001144952.1 Q1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr18:13621233 G>A maps to NM_181481.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr18:13621233 G>A maps to NM_181481.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:9025598 G>A maps to NM_024690.2 T12285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:9025598 G>A maps to NM_024690.2 T12285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:44611291 C>T maps to NM_013398.2 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:44611291 C>T maps to NM_013398.2 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:58574892 C>T maps to NM_007134.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr19:58574892 C>T maps to NM_007134.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr22:19868213 C>A maps to NM_006440.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr22:19868213 C>A maps to NM_006440.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr22:31011459 G>A maps to NM_000355.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chr22:31011459 G>A maps to NM_000355.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:29973757 C>T maps to NM_014271.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:29973757 C>T maps to NM_014271.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:44929218 A>G maps to NM_021140.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:44929218 A>G maps to NM_021140.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:73962088 G>C maps to NM_001008537.2 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:73962088 G>C maps to NM_001008537.2 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:129149013 C>T maps to ENST00000303743 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:129149013 C>T maps to ENST00000303743 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:148037677 C>T maps to NM_002025.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:148037677 C>T maps to NM_002025.3 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:149809882 C>T maps to NM_000252.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:149809882 C>T maps to NM_000252.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:153496063 G>A maps to NM_000513.2 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0EZ-01A-21D-A10S-08 chrX:153496063 G>A maps to NM_000513.2 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:3672129 C>T maps to NM_152492.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:3672129 C>T maps to NM_152492.2 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:11596719 C>T maps to NM_020780.1 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:11596719 C>T maps to NM_020780.1 L1386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:36859514 G>C maps to NM_032881.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:36859514 G>C maps to NM_032881.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:175067711 C>T maps to NM_022093.1 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr1:175067711 C>T maps to NM_022093.1 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr2:74043845 G>T maps to NM_001080474.1 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr2:74043845 G>T maps to NM_001080474.1 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr2:227953428 G>T maps to ENST00000396625 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr2:227953428 G>T maps to ENST00000396625 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:13669332 C>T maps to NM_001165035.1 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:13669332 C>T maps to NM_001165035.1 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:48453975 G>A maps to NM_001130082.1 Y1636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:48453975 G>A maps to NM_001130082.1 Y1636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:48605195 C>A maps to NM_000094.3 G2644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:48605195 C>A maps to NM_000094.3 G2644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:100364942 T>C maps to NM_032787.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:100364942 T>C maps to NM_032787.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:132050576 G>A maps to NM_001134194.1 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr3:132050576 G>A maps to NM_001134194.1 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr4:153253769 C>T maps to NM_033632.2 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr4:153253769 C>T maps to NM_033632.2 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr5:45303772 G>A maps to NM_021072.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr5:45303772 G>A maps to NM_021072.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr5:71494956 C>G maps to NM_005909.3 T1925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr5:71494956 C>G maps to NM_005909.3 T1925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr7:100189392 C>T maps to NM_012172.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr7:100189392 C>T maps to NM_012172.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr7:100491628 G>T maps to NM_000665.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr7:100491628 G>T maps to NM_000665.3 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr9:37746198 C>T maps to NM_014907.2 T1390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr9:37746198 C>T maps to NM_014907.2 T1390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr9:88272366 G>A maps to ENST00000395847 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr9:88272366 G>A maps to ENST00000395847 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr12:7656274 G>A maps to NM_004244.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr12:7656274 G>A maps to NM_004244.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr12:21997777 A>G maps to NM_005691.2 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr12:21997777 A>G maps to NM_005691.2 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr13:48947628 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr13:48947628 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr13:76427231 G>T maps to ENST00000357063 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr13:76427231 G>T maps to ENST00000357063 E1387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr14:77275516 T>C maps to NM_015305.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr14:77275516 T>C maps to NM_015305.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:19547560 C>G maps to NM_014711.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:19547560 C>G maps to NM_014711.4 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:53967949 G>A maps to NM_001080432.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:53967949 G>A maps to NM_001080432.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:70917862 G>A maps to NM_032821.2 A3312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr16:70917862 G>A maps to NM_032821.2 A3312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr18:28576943 G>C maps to NM_001941.3 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr18:28576943 G>C maps to NM_001941.3 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr18:50450131 C>A maps to NM_005215.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr18:50450131 C>A maps to NM_005215.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr19:21300900 G>A maps to NM_182515.3 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr19:21300900 G>A maps to NM_182515.3 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr19:38893807 G>A maps to NM_174905.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr19:38893807 G>A maps to NM_174905.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr20:3147629 C>T maps to NM_014731.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr20:3147629 C>T maps to NM_014731.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr22:16279259 T>C maps to NM_001136213.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr22:16279259 T>C maps to NM_001136213.1 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr22:32647855 G>A maps to NM_014227.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chr22:32647855 G>A maps to NM_014227.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chrX:34657460 G>T maps to NM_031442.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chrX:34657460 G>T maps to NM_031442.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chrX:39933137 T>C maps to NM_001123385.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chrX:39933137 T>C maps to NM_001123385.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chrX:152994805 C>T maps to NM_000033.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F0-01A-12D-A10S-08 chrX:152994805 C>T maps to NM_000033.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:17330837 G>A maps to NM_022089.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:17330837 G>A maps to NM_022089.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:32043027 C>T maps to NM_022164.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:32043027 C>T maps to NM_022164.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:32264126 G>T maps to NM_144569.4 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:32264126 G>T maps to NM_144569.4 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:101194672 T>C maps to NM_001078.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:101194672 T>C maps to NM_001078.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:145608195 C>T maps to NM_006468.6 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:145608195 C>T maps to NM_006468.6 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:201056979 G>A maps to NM_000069.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:201056979 G>A maps to NM_000069.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:207314559 C>T maps to NM_000715.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr1:207314559 C>T maps to NM_000715.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr2:158980393 C>G maps to NM_001135098.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr2:158980393 C>G maps to NM_001135098.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr2:235962411 G>A maps to NM_014521.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr2:235962411 G>A maps to NM_014521.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:48698816 C>T maps to NM_001407.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:48698816 C>T maps to NM_001407.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:142231261 T>G maps to NM_001184.3 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr3:142231261 T>G maps to NM_001184.3 I1564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr4:15569098 C>T maps to NM_001080522.2 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr4:15569098 C>T maps to NM_001080522.2 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr4:55961104 G>A maps to NM_002253.2 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr4:55961104 G>A maps to NM_002253.2 F945F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr5:176025547 C>A maps to NM_052899.2 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr5:176025547 C>A maps to NM_052899.2 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:31838640 G>A maps to NM_025257.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:31838640 G>A maps to NM_025257.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:119226947 G>A maps to NM_014034.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:119226947 G>A maps to NM_014034.2 E119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:167755004 G>A maps to NM_031949.4 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr6:167755004 G>A maps to NM_031949.4 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:18975510 C>G maps to NM_178425.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:18975510 C>G maps to NM_178425.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:21945944 C>A maps to NM_018719.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:21945944 C>A maps to NM_018719.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:100151097 C>G maps to NM_006076.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:100151097 C>G maps to NM_006076.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:124404703 G>T maps to NM_005302.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:124404703 G>T maps to NM_005302.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:151855997 C>A maps to ENST00000355193 E3874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:151855997 C>A maps to ENST00000355193 E3874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:76465275 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:76465275 G>A did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:100403870 G>A maps to NM_017890.3 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:100403870 G>A maps to NM_017890.3 K1007K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:146033635 C>T maps to NM_213605.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr8:146033635 C>T maps to NM_213605.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:20720512 C>T maps to NM_017794.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:20720512 C>T maps to NM_017794.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:35752110 C>T maps to ENST00000456972 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:35752110 C>T maps to ENST00000456972 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:35752708 C>G maps to ENST00000456972 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:35752708 C>G maps to ENST00000456972 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:123620305 C>T maps to NM_015651.1 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:123620305 C>T maps to NM_015651.1 E553E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:139273743 G>C maps to NM_003086.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr9:139273743 G>C maps to NM_003086.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:61729848 C>G maps to NM_001139443.1 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:61729848 C>G maps to NM_001139443.1 S348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:70281228 C>T maps to NM_005231.3 Y538Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:70281228 C>T maps to NM_005231.3 Y538Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:118376453 C>T maps to NM_001197104.1 R3283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:118376453 C>T maps to NM_001197104.1 R3283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:123848194 G>C maps to NM_001004474.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:123848194 G>C maps to NM_001004474.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:125891383 G>C maps to ENST00000392693 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr11:125891383 G>C maps to ENST00000392693 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:4722726 G>A maps to NM_003845.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:4722726 G>A maps to NM_003845.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:49424158 G>A maps to NM_003482.3 Q4635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:49424158 G>A maps to NM_003482.3 Q4635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:49722835 C>T maps to NM_005480.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:49722835 C>T maps to NM_005480.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:119942995 G>T maps to NM_178499.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr12:119942995 G>T maps to NM_178499.3 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:28897020 C>T maps to NM_002019.4 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:28897020 C>T maps to NM_002019.4 K953K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:35619478 C>T maps to ENST00000400445 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:35619478 C>T maps to ENST00000400445 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:43935580 G>A maps to NM_001127615.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr13:43935580 G>A maps to NM_001127615.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:91681827 G>A maps to NM_001102368.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:91681827 G>A maps to NM_001102368.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:91700959 G>A maps to ENST00000238699 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:91700959 G>A maps to ENST00000238699 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:105397200 G>A maps to NM_138790.2 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr14:105397200 G>A maps to NM_138790.2 Q280Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr15:41657736 G>C maps to NM_016359.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr15:41657736 G>C maps to NM_016359.3 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr15:58861006 C>G maps to NM_000236.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr15:58861006 C>G maps to NM_000236.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:601634 C>T maps to NM_005632.2 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:601634 C>T maps to NM_005632.2 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:2155924 G>A maps to NM_001009944.2 Q2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:2155924 G>A maps to NM_001009944.2 Q2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:2813978 G>A maps to NM_016333.3 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr16:2813978 G>A maps to NM_016333.3 S1150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:2265471 C>T maps to NM_014853.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:2265471 C>T maps to NM_014853.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:7214696 C>A maps to NM_001143760.1 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:7214696 C>A maps to NM_001143760.1 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:7701999 G>A maps to NM_020877.2 E2841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:7701999 G>A maps to NM_020877.2 E2841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:10442617 C>T maps to NM_017534.5 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:10442617 C>T maps to NM_017534.5 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:51901323 G>A maps to NM_032559.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:51901323 G>A maps to NM_032559.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:56233156 C>T maps to NM_012374.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:56233156 C>T maps to NM_012374.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:76167699 C>T maps to NM_004710.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr17:76167699 C>T maps to NM_004710.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr18:34387819 C>T maps to NM_015476.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr18:34387819 C>T maps to NM_015476.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:6760800 C>T maps to NM_005490.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:6760800 C>T maps to NM_005490.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:9057195 G>A maps to NM_024690.2 L10084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:9057195 G>A maps to NM_024690.2 L10084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:47349396 G>A maps to NM_004069.3 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:47349396 G>A maps to NM_004069.3 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:51022594 G>A maps to NM_001080457.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr19:51022594 G>A maps to NM_001080457.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:19955571 G>T maps to ENST00000255006 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:19955571 G>T maps to ENST00000255006 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:31699225 T>C maps to NM_182519.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:31699225 T>C maps to NM_182519.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:34242689 G>T maps to NM_001198838.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:34242689 G>T maps to NM_001198838.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:43255221 G>A maps to NM_000022.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr20:43255221 G>A maps to NM_000022.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr21:43413916 C>T maps to NM_020727.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr21:43413916 C>T maps to NM_020727.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:27008145 G>T maps to NM_001887.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:27008145 G>T maps to NM_001887.3 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:38327930 C>T maps to NM_033386.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:38327930 C>T maps to NM_033386.2 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:38328838 C>T maps to NM_033386.2 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr22:38328838 C>T maps to NM_033386.2 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:47041368 C>G maps to NM_005676.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:47041368 C>G maps to NM_005676.3 T571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:47045532 A>T maps to NM_005676.3 K834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:47045532 A>T maps to NM_005676.3 K834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:63413138 G>A maps to NM_152424.3 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:63413138 G>A maps to NM_152424.3 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:70470409 C>T maps to ENST00000373988 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chrX:70470409 C>T maps to ENST00000373988 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:43895746 C>T maps to NM_015284.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:43895746 C>T maps to NM_015284.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:74671226 C>A maps to NM_003838.3 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:74671226 C>A maps to NM_003838.3 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:100459151 C>G maps to ENST00000370153 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:100459151 C>G maps to ENST00000370153 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:158516977 G>A maps to NM_001005189.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:158516977 G>A maps to NM_001005189.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:197390533 C>T maps to NM_201253.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:197390533 C>T maps to NM_201253.2 R526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:202777327 C>A maps to ENST00000367264 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr1:202777327 C>A maps to ENST00000367264 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:1241710 C>T maps to NM_018968.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:1241710 C>T maps to NM_018968.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:27505676 C>T maps to NM_032546.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:27505676 C>T maps to NM_032546.3 C26C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:54159083 G>A maps to NM_014614.2 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:54159083 G>A maps to NM_014614.2 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:141598562 G>A maps to NM_018557.2 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr2:141598562 G>A maps to NM_018557.2 L1680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr3:38039652 G>A maps to NM_015873.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr3:38039652 G>A maps to NM_015873.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr3:160942824 C>A maps to ENST00000472947 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr3:160942824 C>A maps to ENST00000472947 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:1843343 C>T maps to NM_012318.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:1843343 C>T maps to NM_012318.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:57250455 G>A maps to NM_181806.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:57250455 G>A maps to NM_181806.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:74285274 G>A maps to NM_000477.5 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:74285274 G>A maps to NM_000477.5 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:104103930 A>C maps to NM_001813.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:104103930 A>C maps to NM_001813.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:154625549 C>G maps to NM_003264.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:154625549 C>G maps to NM_003264.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:6378551 G>A maps to NM_032286.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:6378551 G>A maps to NM_032286.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:140263523 C>T maps to NM_018904.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:140263523 C>T maps to NM_018904.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:150657199 G>T maps to NM_001145017.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr5:150657199 G>T maps to NM_001145017.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr6:52268631 C>T maps to ENST00000361841 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr6:52268631 C>T maps to ENST00000361841 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr7:44796035 C>T maps to NM_031449.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr7:44796035 C>T maps to NM_031449.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr8:133906094 G>A maps to NM_003235.4 P974P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr8:133906094 G>A maps to NM_003235.4 P974P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:98690413 C>G maps to NM_001010895.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:98690413 C>G maps to NM_001010895.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:100888881 C>G maps to NM_052820.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:100888881 C>G maps to NM_052820.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:117389257 C>A maps to ENST00000374049 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:117389257 C>A maps to ENST00000374049 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:132658258 C>T maps to NM_015033.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:132658258 C>T maps to NM_015033.2 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:137300843 G>A maps to NM_002957.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:137300843 G>A maps to NM_002957.4 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:139391497 G>C maps to NM_017617.3 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr9:139391497 G>C maps to NM_017617.3 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr10:26581832 T>C maps to NM_001134366.1 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr10:26581832 T>C maps to NM_001134366.1 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:397292 C>T maps to NM_007183.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:397292 C>T maps to NM_007183.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:9608063 T>C maps to NM_003390.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:9608063 T>C maps to NM_003390.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:56258183 G>A maps to NM_001005282.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:56258183 G>A maps to NM_001005282.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:66619973 G>C maps to NM_022172.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:66619973 G>C maps to NM_022172.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:67075643 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:67075643 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:71698133 C>T maps to NM_018320.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:71698133 C>T maps to NM_018320.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:86518960 C>T maps to NM_007173.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:86518960 C>T maps to NM_007173.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:103908029 C>G maps to NM_001001711.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr11:103908029 C>G maps to NM_001001711.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:49416551 G>A maps to NM_003482.3 Q5387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:49416551 G>A maps to NM_003482.3 Q5387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:51065078 C>T maps to NM_173602.2 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:51065078 C>T maps to NM_173602.2 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:58021629 C>T maps to NM_001478.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:58021629 C>T maps to NM_001478.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:69109477 C>G maps to NM_020401.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:69109477 C>G maps to NM_020401.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:70932749 G>C maps to NM_001109754.1 L1941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:70932749 G>C maps to NM_001109754.1 L1941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:111655741 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr12:111655741 G>T did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr14:63246454 C>G maps to NM_139318.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr14:63246454 C>G maps to NM_139318.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr14:95033346 C>G maps to NM_006215.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr14:95033346 C>G maps to NM_006215.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:28211932 G>A maps to NM_000275.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:28211932 G>A maps to NM_000275.2 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:30011183 G>A maps to NM_003257.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:30011183 G>A maps to NM_003257.3 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:68504195 G>A maps to NM_017882.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:68504195 G>A maps to NM_017882.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:90622958 C>T maps to NM_198526.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:90622958 C>T maps to NM_198526.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:91421500 C>T maps to NM_002569.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr15:91421500 C>T maps to NM_002569.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:347182 C>A maps to NM_003502.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:347182 C>A maps to NM_003502.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:24988547 G>A maps to NM_001006634.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:24988547 G>A maps to NM_001006634.1 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:28137113 C>G maps to NM_015171.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr16:28137113 C>G maps to NM_015171.2 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:4863784 G>A maps to NM_004890.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:4863784 G>A maps to NM_004890.2 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:9559743 C>T maps to NM_153210.3 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:9559743 C>T maps to NM_153210.3 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:40936119 C>T maps to NM_032387.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:40936119 C>T maps to NM_032387.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:65340840 C>A maps to NM_002816.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:65340840 C>A maps to NM_002816.3 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:66933152 A>G maps to NM_007168.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:66933152 A>G maps to NM_007168.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:71197987 C>T maps to NM_018714.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr17:71197987 C>T maps to NM_018714.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2130434 C>T maps to ENST00000355272 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2130434 C>T maps to ENST00000355272 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2216302 G>A maps to ENST00000221482 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2216302 G>A maps to ENST00000221482 K649K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2216318 G>T maps to ENST00000221482 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:2216318 G>T maps to ENST00000221482 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:12826059 G>A maps to NM_001136196.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:12826059 G>A maps to NM_001136196.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:49971799 C>T maps to NM_153329.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:49971799 C>T maps to NM_153329.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:51582811 G>A maps to NM_022046.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:51582811 G>A maps to NM_022046.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:54656168 C>A maps to NM_014516.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr19:54656168 C>A maps to NM_014516.3 I570I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr20:37353312 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr20:37353312 C>G did not map to a codon.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr21:28214228 G>A maps to NM_006988.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr21:28214228 G>A maps to NM_006988.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr21:43767667 G>A maps to NM_005423.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr21:43767667 G>A maps to NM_005423.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr22:30748977 G>C maps to NM_005877.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr22:30748977 G>C maps to NM_005877.4 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr22:46792542 G>A maps to NM_014246.1 C1934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr22:46792542 G>A maps to NM_014246.1 C1934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:44938511 C>T maps to NM_021140.2 I1020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:44938511 C>T maps to NM_021140.2 I1020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:53603878 T>C maps to ENST00000276009 A1955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:53603878 T>C maps to ENST00000276009 A1955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:114141689 C>T maps to NM_000868.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:114141689 C>T maps to NM_000868.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:140995584 C>T maps to NM_005462.4 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:140995584 C>T maps to NM_005462.4 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:144337273 G>A maps to NM_001009614.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chrX:144337273 G>A maps to NM_001009614.2 A53A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-C4-A0F6-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-C4-A0F6-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr1:200968595 T>C did not map to a codon.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr1:200968595 T>C did not map to a codon.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr1:226340228 C>T maps to NM_022735.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr1:226340228 C>T maps to NM_022735.3 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:1983501 C>T maps to ENST00000399161 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:1983501 C>T maps to ENST00000399161 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:79971688 A>T maps to ENST00000402739 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:79971688 A>T maps to ENST00000402739 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:196865505 G>A maps to NM_018897.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr2:196865505 G>A maps to NM_018897.2 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:53213623 G>A maps to NM_212539.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:53213623 G>A maps to NM_212539.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:63985135 G>A maps to NM_001177387.1 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:63985135 G>A maps to NM_001177387.1 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:195511814 G>A maps to NM_018406.5 T2212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr3:195511814 G>A maps to NM_018406.5 T2212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr4:68964664 A>G maps to NM_207407.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr4:68964664 A>G maps to NM_207407.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr4:100479210 A>G maps to NM_001134666.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr4:100479210 A>G maps to NM_001134666.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr5:6633925 C>T maps to NM_001047.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr5:6633925 C>T maps to NM_001047.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:43472737 T>C maps to NM_001146016.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:43472737 T>C maps to NM_001146016.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:44216417 C>T maps to NM_007355.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:44216417 C>T maps to NM_007355.2 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:109980579 G>A maps to NM_001145128.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr6:109980579 G>A maps to NM_001145128.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:4794200 C>T maps to ENST00000450194 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:4794200 C>T maps to ENST00000450194 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:43484651 G>A maps to NM_015052.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:43484651 G>A maps to NM_015052.3 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:100187840 C>G maps to NM_012172.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr7:100187840 C>G maps to NM_012172.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:73480334 A>G maps to NM_004770.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:73480334 A>G maps to NM_004770.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:77776410 T>C maps to NM_024721.4 V3487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:77776410 T>C maps to NM_024721.4 V3487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:128429169 C>T maps to NM_001159542.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:128429169 C>T maps to NM_001159542.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:139734290 C>T maps to NM_152888.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr8:139734290 C>T maps to NM_152888.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:64035012 G>A maps to NM_000932.2 E1230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:64035012 G>A maps to NM_000932.2 E1230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:64525783 G>A maps to NM_005609.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:64525783 G>A maps to NM_005609.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:94231643 T>C maps to NM_017704.2 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:94231643 T>C maps to NM_017704.2 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:121039496 G>C maps to NM_005422.2 T1954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr11:121039496 G>C maps to NM_005422.2 T1954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr12:9006742 T>A maps to NM_144670.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr12:9006742 T>A maps to NM_144670.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr12:52962080 G>A maps to NM_175053.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr12:52962080 G>A maps to NM_175053.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr14:78184463 G>A maps to NM_012245.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr14:78184463 G>A maps to NM_012245.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr16:53679567 C>T maps to NM_015272.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr16:53679567 C>T maps to NM_015272.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr17:27899298 C>G maps to NM_138349.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr17:27899298 C>G maps to NM_138349.2 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr19:4499522 G>A maps to ENST00000301284 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr19:4499522 G>A maps to ENST00000301284 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr19:11486190 G>A maps to NM_175871.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr19:11486190 G>A maps to NM_175871.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr21:46951333 G>A maps to NM_194255.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr21:46951333 G>A maps to NM_194255.1 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr22:37414344 G>A maps to NM_003312.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chr22:37414344 G>A maps to NM_003312.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chrX:22291956 G>A maps to NM_152577.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F7-01A-11D-A10S-08 chrX:22291956 G>A maps to NM_152577.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:6634782 G>A maps to NM_138697.3 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:6634782 G>A maps to NM_138697.3 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:16111107 C>G maps to NM_017556.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:16111107 C>G maps to NM_017556.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:16111143 G>T maps to NM_017556.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:16111143 G>T maps to NM_017556.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:27101308 G>T maps to NM_006015.4 E1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:27101308 G>T maps to NM_006015.4 E1531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:45115331 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:45115331 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:52704804 C>T maps to NM_004799.2 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:52704804 C>T maps to NM_004799.2 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:52705107 C>T maps to NM_004799.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:52705107 C>T maps to NM_004799.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:149906109 G>A maps to NM_001145862.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:149906109 G>A maps to NM_001145862.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:152082179 G>C maps to NM_007113.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:152082179 G>C maps to NM_007113.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:152285756 C>T maps to NM_002016.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:152285756 C>T maps to NM_002016.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:186088321 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:186088321 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:186319406 G>C maps to NM_003292.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:186319406 G>C maps to NM_003292.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:207039848 C>A maps to NM_018724.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr1:207039848 C>A maps to NM_018724.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:11911646 G>A maps to ENST00000396099 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:11911646 G>A maps to ENST00000396099 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:25990451 T>A maps to NM_018263.4 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:25990451 T>A maps to NM_018263.4 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:27016086 C>G maps to NM_001809.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:27016086 C>G maps to NM_001809.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:27360612 G>A maps to NM_178553.3 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:27360612 G>A maps to NM_178553.3 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:100019386 G>A maps to NM_016316.2 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:100019386 G>A maps to NM_016316.2 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:128066316 G>C maps to NM_006609.3 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:128066316 G>C maps to NM_006609.3 S493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:160035371 C>T maps to NM_033394.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:160035371 C>T maps to NM_033394.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:191818301 G>C maps to NM_014905.3 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr2:191818301 G>C maps to NM_014905.3 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:33194714 G>C maps to NM_015551.1 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:33194714 G>C maps to NM_015551.1 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:47158212 G>A maps to NM_014159.6 R1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:47158212 G>A maps to NM_014159.6 R1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:50379108 C>T maps to NM_015896.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:50379108 C>T maps to NM_015896.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:63938122 C>T maps to NM_001177387.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:63938122 C>T maps to NM_001177387.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:69027582 G>A maps to ENST00000383701 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:69027582 G>A maps to ENST00000383701 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:98188797 A>C maps to NM_001004736.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:98188797 A>C maps to NM_001004736.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:109050828 C>T maps to NM_018189.3 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:109050828 C>T maps to NM_018189.3 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:121413279 C>T maps to ENST00000393667 Q2030Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:121413279 C>T maps to ENST00000393667 Q2030Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:122811200 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:122811200 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:146311796 C>T maps to NM_001085420.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:146311796 C>T maps to NM_001085420.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:172643145 C>G maps to NM_031955.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:172643145 C>G maps to NM_031955.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:179448466 C>G maps to NM_003940.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:179448466 C>G maps to NM_003940.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:39905709 C>T maps to NM_001100399.1 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:39905709 C>T maps to NM_001100399.1 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:83996451 C>T maps to ENST00000503682 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:83996451 C>T maps to ENST00000503682 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:142147921 G>A maps to NM_014487.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:142147921 G>A maps to NM_014487.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:174254743 G>A maps to NM_002129.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:174254743 G>A maps to NM_002129.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:183675803 G>C maps to NM_001080477.1 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:183675803 G>C maps to NM_001080477.1 R1428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:186278862 C>T maps to NM_031953.2 Q711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr4:186278862 C>T maps to NM_031953.2 Q711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:14607517 C>A maps to NM_019018.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:14607517 C>A maps to NM_019018.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:37045559 T>A maps to NM_133433.3 L2120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:37045559 T>A maps to NM_133433.3 L2120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:37703083 C>G maps to NM_018034.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:37703083 C>G maps to NM_018034.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:38484883 G>A maps to NM_002310.5 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:38484883 G>A maps to NM_002310.5 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:43161884 A>G maps to ENST00000509156 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:43161884 A>G maps to ENST00000509156 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:74970316 G>C maps to NM_001099271.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:74970316 G>C maps to NM_001099271.1 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:127609547 G>A maps to NM_001999.3 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:127609547 G>A maps to NM_001999.3 T2608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:145239352 C>T maps to NM_001080516.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr5:145239352 C>T maps to NM_001080516.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:17669712 G>T maps to ENST00000430136 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:17669712 G>T maps to ENST00000430136 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:24503594 C>T maps to NM_170740.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:24503594 C>T maps to NM_170740.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:33391252 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:33391252 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:54025593 C>G maps to ENST00000502396 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:54025593 C>G maps to ENST00000502396 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:108985340 C>T maps to NM_001455.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr6:108985340 C>T maps to NM_001455.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:23810676 G>T maps to NM_031414.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:23810676 G>T maps to NM_031414.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:27135405 G>A maps to NM_005522.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:27135405 G>A maps to NM_005522.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:127341353 C>G maps to NM_014390.2 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:127341353 C>G maps to NM_014390.2 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:146536941 C>G maps to NM_014141.5 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr7:146536941 C>G maps to NM_014141.5 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:442628 C>A maps to NM_175075.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:442628 C>A maps to NM_175075.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:8175846 C>A maps to NM_001080826.1 T1346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:8175846 C>A maps to NM_001080826.1 T1346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:54147421 G>A maps to NM_000912.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:54147421 G>A maps to NM_000912.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:110535086 C>T maps to ENST00000426474 Q4101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:110535086 C>T maps to ENST00000426474 Q4101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:124250181 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr8:124250181 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:90537506 C>A maps to NM_001145124.1 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:90537506 C>A maps to NM_001145124.1 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:95155526 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:95155526 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:96415472 C>T maps to NM_005392.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:96415472 C>T maps to NM_005392.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:125797111 C>T maps to NM_005294.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:125797111 C>T maps to NM_005294.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:135786886 G>A maps to NM_000368.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:135786886 G>A maps to NM_000368.4 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:137676851 C>T maps to NM_000093.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:137676851 C>T maps to NM_000093.3 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:138439762 C>T maps to NM_014582.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr9:138439762 C>T maps to NM_014582.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:12071354 T>C maps to NM_015542.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:12071354 T>C maps to NM_015542.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:45907637 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:45907637 G>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:50857601 C>T maps to NM_020549.4 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:50857601 C>T maps to NM_020549.4 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:68040317 C>T maps to NM_013266.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:68040317 C>T maps to NM_013266.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:74619016 C>G maps to NM_138357.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:74619016 C>G maps to NM_138357.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:121431903 C>T maps to NM_004281.3 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:121431903 C>T maps to NM_004281.3 N215N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:129905873 G>A maps to NM_002417.4 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:129905873 G>A maps to NM_002417.4 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:5372784 A>C maps to NM_001004750.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:5372784 A>C maps to NM_001004750.1 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:12248644 C>G maps to NM_014632.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:12248644 C>G maps to NM_014632.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:14502616 T>C maps to NM_001144061.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:14502616 T>C maps to NM_001144061.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:28232682 C>G maps to NM_001113528.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:28232682 C>G maps to NM_001113528.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:66082773 G>A maps to NM_020404.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:66082773 G>A maps to NM_020404.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:123900607 C>T maps to NM_001004464.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:123900607 C>T maps to NM_001004464.1 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:128781389 G>C maps to NM_000890.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr11:128781389 G>C maps to NM_000890.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:22015984 C>T maps to NM_005691.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:22015984 C>T maps to NM_005691.2 R747R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:43826584 G>T maps to ENST00000389420 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:43826584 G>T maps to ENST00000389420 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:56995426 G>C maps to NM_013449.3 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:56995426 G>C maps to NM_013449.3 S1327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:102572446 C>T maps to NM_017915.3 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:102572446 C>T maps to NM_017915.3 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:106632981 G>A maps to NM_006825.3 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:106632981 G>A maps to NM_006825.3 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:131488788 G>A maps to NM_198827.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr12:131488788 G>A maps to NM_198827.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:30106970 G>C maps to NM_003045.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:30106970 G>C maps to NM_003045.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:31543164 C>T maps to NM_152325.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:31543164 C>T maps to NM_152325.1 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:32914960 C>T maps to NM_000059.3 Q2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:32914960 C>T maps to NM_000059.3 Q2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:41910843 C>T maps to NM_024561.4 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:41910843 C>T maps to NM_024561.4 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:103419690 C>A maps to NM_138779.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr13:103419690 C>A maps to NM_138779.3 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:36230212 C>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:36230212 C>A did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:50583165 G>A maps to NM_024558.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:50583165 G>A maps to NM_024558.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:74360608 C>A maps to NM_021188.1 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr14:74360608 C>A maps to NM_021188.1 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:23889946 G>C maps to NM_019066.4 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:23889946 G>C maps to NM_019066.4 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:34649514 G>A maps to ENST00000438749 K1092K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:34649514 G>A maps to ENST00000438749 K1092K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:43025296 G>A maps to NM_138477.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:43025296 G>A maps to NM_138477.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:74912487 G>A maps to NM_001130028.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:74912487 G>A maps to NM_001130028.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:89873443 C>T maps to NM_002693.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr15:89873443 C>T maps to NM_002693.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:28878107 G>A maps to NM_001145795.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:28878107 G>A maps to NM_001145795.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:49671946 G>A maps to NM_015069.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:49671946 G>A maps to NM_015069.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:57065330 C>T maps to NM_032206.3 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:57065330 C>T maps to NM_032206.3 I811I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:67909845 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:67909845 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:77859261 C>T maps to NM_020927.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:77859261 C>T maps to NM_020927.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:81249934 G>A maps to NM_052892.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr16:81249934 G>A maps to NM_052892.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:1582370 G>A maps to NM_006445.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:1582370 G>A maps to NM_006445.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:10535903 G>C maps to NM_002470.2 L1615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:10535903 G>C maps to NM_002470.2 L1615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17699981 C>G maps to ENST00000395776 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17699981 C>G maps to ENST00000395776 V1240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17700284 C>G maps to ENST00000395776 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17700284 C>G maps to ENST00000395776 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17701367 C>T maps to ENST00000395776 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:17701367 C>T maps to ENST00000395776 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:26820717 C>T maps to NM_001145975.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:26820717 C>T maps to NM_001145975.1 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:27421805 C>T maps to NM_078471.3 Q1524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:27421805 C>T maps to NM_078471.3 Q1524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:35512648 G>A maps to NM_198834.1 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:35512648 G>A maps to NM_198834.1 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:37046754 C>T maps to NM_006148.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:37046754 C>T maps to NM_006148.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:39262230 C>A maps to ENST00000377731 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:39262230 C>A maps to ENST00000377731 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:48445521 G>C maps to NM_016504.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:48445521 G>C maps to NM_016504.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:56349050 G>A maps to ENST00000340482 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:56349050 G>A maps to ENST00000340482 I697I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:74307741 G>A maps to NM_002766.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:74307741 G>A maps to NM_002766.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:78343328 C>T maps to NM_020914.4 F4110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:78343328 C>T maps to NM_020914.4 F4110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:80439026 C>T maps to ENST00000374611 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr17:80439026 C>T maps to ENST00000374611 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:12702510 G>A maps to NM_024899.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:12702510 G>A maps to NM_024899.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:44559493 C>T maps to NM_016427.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:44559493 C>T maps to NM_016427.2 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:44589672 C>T maps to ENST00000356157 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:44589672 C>T maps to ENST00000356157 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:74587571 C>T maps to NM_007345.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr18:74587571 C>T maps to NM_007345.3 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:17305658 C>G maps to NM_004145.3 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:17305658 C>G maps to NM_004145.3 V1141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:17440961 C>T maps to NM_020959.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:17440961 C>T maps to NM_020959.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:20117296 C>T maps to NM_033196.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:20117296 C>T maps to NM_033196.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:39868168 G>A maps to NM_018028.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:39868168 G>A maps to NM_018028.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:43680124 G>A maps to ENST00000270059 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:43680124 G>A maps to ENST00000270059 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:44896513 G>A maps to NM_152354.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:44896513 G>A maps to NM_152354.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:54667457 G>A maps to NM_001145303.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:54667457 G>A maps to NM_001145303.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:55147017 G>A maps to ENST00000427581 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr19:55147017 G>A maps to ENST00000427581 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:44640216 C>G maps to NM_004994.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:44640216 C>G maps to NM_004994.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:47841696 C>T maps to NM_017895.7 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:47841696 C>T maps to NM_017895.7 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:57251298 C>T maps to NM_001001433.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:57251298 C>T maps to NM_001001433.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:61944554 C>T maps to ENST00000326996 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr20:61944554 C>T maps to ENST00000326996 Y728Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr21:40547516 C>G maps to NM_003720.2 *289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr21:40547516 C>G maps to NM_003720.2 *289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:21140346 G>T maps to NM_000185.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:21140346 G>T maps to NM_000185.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:30806615 C>G maps to NM_012429.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:30806615 C>G maps to NM_012429.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:42523514 G>A maps to NM_000106.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr22:42523514 G>A maps to NM_000106.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chrX:48895742 G>A maps to ENST00000336239 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chrX:48895742 G>A maps to ENST00000336239 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chrX:129206252 C>T maps to NM_001127197.1 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chrX:129206252 C>T maps to NM_001127197.1 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:33363894 C>G maps to NM_033504.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:33363894 C>G maps to NM_033504.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:44474197 C>T maps to NM_201649.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:44474197 C>T maps to NM_201649.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:54343991 G>T maps to NM_018982.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:54343991 G>T maps to NM_018982.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:56990202 C>T maps to NM_003713.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:56990202 C>T maps to NM_003713.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:57481003 C>A maps to ENST00000371231 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:57481003 C>A maps to ENST00000371231 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:82432118 G>A maps to ENST00000370717 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:82432118 G>A maps to ENST00000370717 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:93677789 A>G maps to NM_206886.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:93677789 A>G maps to NM_206886.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:103544383 T>C maps to NM_080629.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:103544383 T>C maps to NM_080629.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:112524481 G>C maps to ENST00000315987 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:112524481 G>C maps to ENST00000315987 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:150477197 C>T maps to NM_025150.3 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:150477197 C>T maps to NM_025150.3 C603C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151338295 C>T maps to ENST00000435071 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151338295 C>T maps to ENST00000435071 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151378786 G>A maps to NM_015100.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151378786 G>A maps to NM_015100.3 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151506504 C>A maps to NM_020770.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151506504 C>A maps to NM_020770.2 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151801934 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:151801934 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:152749145 C>G maps to NM_178354.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:152749145 C>G maps to NM_178354.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:153724859 C>T maps to ENST00000428986 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:153724859 C>T maps to ENST00000428986 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:168278088 C>G maps to NM_005149.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:168278088 C>G maps to NM_005149.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:248004358 C>A maps to NM_001001959.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr1:248004358 C>A maps to NM_001001959.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:26950988 C>T maps to NM_002246.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:26950988 C>T maps to NM_002246.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:85097588 G>A maps to ENST00000409520 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:85097588 G>A maps to ENST00000409520 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:85097648 G>A maps to ENST00000409520 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:85097648 G>A maps to ENST00000409520 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:86437694 C>T maps to NM_016622.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:86437694 C>T maps to NM_016622.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:128412050 G>A maps to NM_017980.4 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:128412050 G>A maps to NM_017980.4 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:179629029 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:179629029 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:190636561 G>C maps to NM_016467.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:190636561 G>C maps to NM_016467.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:203420418 C>G maps to NM_001204.6 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:203420418 C>G maps to NM_001204.6 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:203650666 G>C maps to NM_138468.4 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:203650666 G>C maps to NM_138468.4 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:212530178 G>T maps to NM_005235.2 C580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:212530178 G>T maps to NM_005235.2 C580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:241569479 C>G maps to NM_001195381.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr2:241569479 C>G maps to NM_001195381.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:9979320 G>A maps to NM_001077415.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:9979320 G>A maps to NM_001077415.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:69153636 G>A maps to NM_006407.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:69153636 G>A maps to NM_006407.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:124413263 G>A maps to NM_001024660.3 R2497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:124413263 G>A maps to NM_001024660.3 R2497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:141162246 T>G maps to NM_001080412.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:141162246 T>G maps to NM_001080412.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:156232887 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:156232887 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:184429333 C>T maps to NM_022149.4 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:184429333 C>T maps to NM_022149.4 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:193029619 G>A maps to NM_198505.2 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr3:193029619 G>A maps to NM_198505.2 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr4:156136152 C>A maps to NM_000910.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr4:156136152 C>A maps to NM_000910.2 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr4:178281776 C>T maps to NM_018248.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr4:178281776 C>T maps to NM_018248.2 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:462320 G>T maps to ENST00000315013 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:462320 G>T maps to ENST00000315013 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:43547974 G>C maps to NM_006451.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:43547974 G>C maps to NM_006451.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:70786809 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:70786809 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:95743997 C>G maps to NM_000439.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:95743997 C>G maps to NM_000439.4 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:154346441 C>T maps to NM_014180.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:154346441 C>T maps to NM_014180.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:178506305 G>C maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr5:178506305 G>C maps to NM_014594.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:28093490 G>C maps to NM_025231.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:28093490 G>C maps to NM_025231.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:32014186 C>T maps to ENST00000375244 V3457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:32014186 C>T maps to ENST00000375244 V3457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:35773575 C>G maps to NM_182548.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:35773575 C>G maps to NM_182548.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:130413971 C>G maps to NM_032438.2 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:130413971 C>G maps to NM_032438.2 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:130762700 C>G maps to NM_052913.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:130762700 C>G maps to NM_052913.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:152771878 G>A maps to NM_182961.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr6:152771878 G>A maps to NM_182961.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:1024673 G>A maps to NM_017781.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:1024673 G>A maps to NM_017781.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:2472654 G>C maps to NM_018641.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:2472654 G>C maps to NM_018641.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:31793150 C>T maps to NM_001191057.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:31793150 C>T maps to NM_001191057.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:33384190 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:33384190 A>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:41739708 T>C maps to NM_002192.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:41739708 T>C maps to NM_002192.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:43917867 C>G maps to NM_001077663.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:43917867 C>G maps to NM_001077663.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:92732368 C>T maps to NM_017654.3 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:92732368 C>T maps to NM_017654.3 E1014E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:114299625 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:114299625 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:129110494 C>G maps to ENST00000450266 S687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:129110494 C>G maps to ENST00000450266 S687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:143141090 C>T maps to NM_177437.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr7:143141090 C>T maps to NM_177437.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:1728459 G>A maps to NM_018941.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:1728459 G>A maps to NM_018941.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:10555322 G>A maps to NM_001040032.1 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:10555322 G>A maps to NM_001040032.1 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:35541108 C>T maps to ENST00000416672 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:35541108 C>T maps to ENST00000416672 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:39604117 T>A maps to NM_001464.3 K683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:39604117 T>A maps to NM_001464.3 K683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:55534675 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:55534675 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:99961626 C>A maps to ENST00000457907 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:99961626 C>A maps to ENST00000457907 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:145693254 C>G maps to NM_145754.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr8:145693254 C>G maps to NM_145754.2 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:20620761 G>A maps to NM_004529.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:20620761 G>A maps to NM_004529.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:79890499 A>C maps to ENST00000376646 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:79890499 A>C maps to ENST00000376646 R867R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:133927971 G>C maps to ENST00000355048 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:133927971 G>C maps to ENST00000355048 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:135601227 G>C maps to NM_152572.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:135601227 G>C maps to NM_152572.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:135702365 G>C maps to NM_152572.2 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr9:135702365 G>C maps to NM_152572.2 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:11505381 G>A maps to NM_001080491.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:11505381 G>A maps to NM_001080491.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:53458274 G>C maps to NM_015235.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:53458274 G>C maps to NM_015235.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:97775977 C>T maps to NM_001159747.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:97775977 C>T maps to NM_001159747.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:105495507 G>T maps to ENST00000369774 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:105495507 G>T maps to ENST00000369774 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:121156214 T>A maps to NM_005308.2 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:121156214 T>A maps to NM_005308.2 Y90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:121541204 A>G maps to NM_014937.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr10:121541204 A>G maps to NM_014937.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:47364472 G>A maps to ENST00000399249 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:47364472 G>A maps to ENST00000399249 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:57080262 G>A maps to NM_033396.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:57080262 G>A maps to NM_033396.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:64427939 C>T maps to NM_015080.3 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:64427939 C>T maps to NM_015080.3 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:64502636 G>A maps to ENST00000320253 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr11:64502636 G>A maps to ENST00000320253 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:420230 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:420230 C>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:15803940 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:15803940 C>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:32480489 G>A maps to NM_001714.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:32480489 G>A maps to NM_001714.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:51845972 G>T maps to NM_001039960.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:51845972 G>T maps to NM_001039960.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:52882203 C>T maps to NM_005554.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:52882203 C>T maps to NM_005554.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:112666448 A>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr12:112666448 A>G did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:23915125 A>G maps to NM_014363.4 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:23915125 A>G maps to NM_014363.4 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:41705449 G>A maps to NM_152903.4 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:41705449 G>A maps to NM_152903.4 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:73636552 G>A maps to NM_001730.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr13:73636552 G>A maps to NM_001730.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr14:25101099 G>A maps to ENST00000382542 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr14:25101099 G>A maps to ENST00000382542 C222C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr14:77242312 C>T maps to NM_014909.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr14:77242312 C>T maps to NM_014909.4 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr15:43339471 G>A maps to NM_174916.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr15:43339471 G>A maps to NM_174916.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr15:54435218 C>T maps to ENST00000260323 S996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr15:54435218 C>T maps to ENST00000260323 S996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:11855264 A>G maps to NM_014153.3 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:11855264 A>G maps to NM_014153.3 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:66847710 G>C maps to ENST00000359087 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:66847710 G>C maps to ENST00000359087 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:67695397 C>A maps to NM_016948.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:67695397 C>A maps to NM_016948.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:67696108 G>C maps to NM_016948.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:67696108 G>C maps to NM_016948.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:71668135 C>T maps to NM_052858.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:71668135 C>T maps to NM_052858.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:84135447 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr16:84135447 G>C did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:5086348 C>T maps to NM_032530.1 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:5086348 C>T maps to NM_032530.1 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:7577121 C>T maps to NM_001126112.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:7577121 C>T maps to NM_001126112.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:59763272 G>A maps to NM_032043.2 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:59763272 G>A maps to NM_032043.2 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:60023933 G>C maps to NM_005121.2 L2140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr17:60023933 G>C maps to NM_005121.2 L2140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:1800006 C>A maps to NM_138813.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:1800006 C>A maps to NM_138813.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:8808754 G>C maps to NM_178525.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:8808754 G>C maps to NM_178525.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:10671687 C>T maps to NM_023008.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:10671687 C>T maps to NM_023008.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:40030086 C>T maps to NM_153232.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:40030086 C>T maps to NM_153232.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:40886913 C>T maps to NM_144685.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:40886913 C>T maps to NM_144685.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:44778141 G>A maps to NM_181756.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:44778141 G>A maps to NM_181756.1 Q443Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:49657669 G>T maps to NM_002152.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:49657669 G>T maps to NM_002152.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:49692257 C>G maps to NM_017636.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:49692257 C>G maps to NM_017636.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:54823807 G>A maps to NM_021250.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr19:54823807 G>A maps to NM_021250.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr21:16338391 C>A maps to NM_003489.3 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr21:16338391 C>A maps to NM_003489.3 E708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr21:16340219 C>T maps to NM_003489.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr21:16340219 C>T maps to NM_003489.3 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:17449259 C>T maps to NM_001037814.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:17449259 C>T maps to NM_001037814.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:36661302 C>T maps to NM_145343.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:36661302 C>T maps to NM_145343.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:40066080 C>T maps to NM_021096.3 F1411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:40066080 C>T maps to NM_021096.3 F1411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:50869672 C>G maps to ENST00000216061 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chr22:50869672 C>G maps to ENST00000216061 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chrX:12939591 G>A maps to ENST00000311912 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chrX:12939591 G>A maps to ENST00000311912 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chrX:138612919 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chrX:138612919 G>T did not map to a codon.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chrX:153128147 G>A maps to NM_000425.3 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HS-01A-11D-A13W-08 chrX:153128147 G>A maps to NM_000425.3 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:18152500 C>G maps to NM_030812.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:18152500 C>G maps to NM_030812.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:50666657 T>C maps to NM_021952.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:50666657 T>C maps to NM_021952.3 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:99772548 C>A maps to NM_014839.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:99772548 C>A maps to NM_014839.4 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:156212940 C>A maps to NM_199173.4 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:156212940 C>A maps to NM_199173.4 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:158670234 C>A maps to NM_001005279.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:158670234 C>A maps to NM_001005279.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:158670235 C>G maps to NM_001005279.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:158670235 C>G maps to NM_001005279.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:181018368 G>A maps to NM_001531.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:181018368 G>A maps to NM_001531.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:205538364 C>T maps to NM_181644.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr1:205538364 C>T maps to NM_181644.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:3627747 C>T maps to NM_001011.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:3627747 C>T maps to NM_001011.3 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:16085628 G>T maps to NM_005378.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:16085628 G>T maps to NM_005378.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:27551029 C>T maps to NM_001521.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:27551029 C>T maps to NM_001521.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:138414423 T>C maps to ENST00000272643 D1391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:138414423 T>C maps to ENST00000272643 D1391D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:215854126 C>T maps to NM_173076.2 W1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr2:215854126 C>T maps to NM_173076.2 W1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:113145000 G>C maps to NM_001164496.1 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:113145000 G>C maps to NM_001164496.1 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:121345736 C>T maps to NM_016298.3 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:121345736 C>T maps to NM_016298.3 R704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:150916248 G>A maps to NM_013308.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr3:150916248 G>A maps to NM_013308.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr4:104061056 A>G maps to NM_001813.2 L2031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr4:104061056 A>G maps to NM_001813.2 L2031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr4:183696287 C>T maps to NM_001080477.1 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr4:183696287 C>T maps to NM_001080477.1 V1762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:33576734 G>A maps to NM_030955.2 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:33576734 G>A maps to NM_030955.2 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:40843578 A>G maps to NM_032587.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:40843578 A>G maps to NM_032587.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:101631644 G>A maps to NM_180991.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:101631644 G>A maps to NM_180991.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:150934192 G>A maps to NM_001447.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:150934192 G>A maps to NM_001447.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:176314050 T>A maps to NM_002115.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr5:176314050 T>A maps to NM_002115.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:75977362 T>C maps to NM_018247.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:75977362 T>C maps to NM_018247.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:80723065 G>T maps to NM_003318.4 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:80723065 G>T maps to NM_003318.4 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:147704099 C>G maps to NM_001127715.1 S1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr6:147704099 C>G maps to NM_001127715.1 S1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr7:44190671 G>A maps to NM_000162.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr7:44190671 G>A maps to NM_000162.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr8:25234818 A>G did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr8:25234818 A>G did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr9:133911630 C>T maps to ENST00000355048 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr9:133911630 C>T maps to ENST00000355048 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr9:137777142 C>A maps to NM_004108.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr9:137777142 C>A maps to NM_004108.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:15600155 G>A maps to NM_003638.1 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:15600155 G>A maps to NM_003638.1 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:15760852 G>A maps to NM_003638.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:15760852 G>A maps to NM_003638.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:21804177 A>T maps to NM_207371.3 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:21804177 A>T maps to NM_207371.3 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:43662479 C>T maps to NM_018590.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:43662479 C>T maps to NM_018590.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:61829046 T>C maps to NM_020987.2 K3864K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr10:61829046 T>C maps to NM_020987.2 K3864K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:21592404 T>C maps to NM_006157.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:21592404 T>C maps to NM_006157.3 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:32635178 A>G maps to NM_001008391.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:32635178 A>G maps to NM_001008391.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:56230094 G>T maps to NM_001004743.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr11:56230094 G>T maps to NM_001004743.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:8083899 G>T maps to NM_006931.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:8083899 G>T maps to NM_006931.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:91347835 G>A maps to NM_152638.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:91347835 G>A maps to NM_152638.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:121706439 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr12:121706439 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:47469987 T>C maps to NM_000621.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:47469987 T>C maps to NM_000621.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:48947628 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:48947628 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:67799770 G>A maps to NM_203487.2 D934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:67799770 G>A maps to NM_203487.2 D934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr14:20612220 G>T maps to NM_001004724.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr14:20612220 G>T maps to NM_001004724.1 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr14:74756768 T>A maps to NM_005050.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr14:74756768 T>A maps to NM_005050.3 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr15:101436229 C>A maps to NM_000693.2 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr15:101436229 C>A maps to NM_000693.2 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr16:61935121 C>A maps to NM_001796.2 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr16:61935121 C>A maps to NM_001796.2 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr16:86601424 C>T maps to NM_005251.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr16:86601424 C>T maps to NM_005251.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:39659034 G>A maps to NM_153490.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:39659034 G>A maps to NM_153490.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:68171212 C>T maps to NM_000891.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr17:68171212 C>T maps to NM_000891.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2290292 G>A maps to NM_001101391.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2290292 G>A maps to NM_001101391.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2433946 G>A maps to NM_032737.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2433946 G>A maps to NM_032737.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2433964 G>A maps to NM_032737.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:2433964 G>A maps to NM_032737.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:3623700 G>A maps to NM_021231.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:3623700 G>A maps to NM_021231.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:12691721 G>A maps to NM_020714.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr19:12691721 G>A maps to NM_020714.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr20:45022240 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr20:45022240 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr20:61572868 A>G maps to NM_017896.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr20:61572868 A>G maps to NM_017896.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr21:17203739 C>T maps to ENST00000285681 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr21:17203739 C>T maps to ENST00000285681 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr21:46910214 C>T maps to ENST00000359759 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr21:46910214 C>T maps to ENST00000359759 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:7995115 C>A maps to NM_001561.5 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:7995115 C>A maps to NM_001561.5 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:27059259 C>T maps to NM_006015.4 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:27059259 C>T maps to NM_006015.4 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:53370431 C>G maps to ENST00000371522 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:53370431 C>G maps to ENST00000371522 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:155720457 C>A maps to ENST00000368331 E2215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:155720457 C>A maps to ENST00000368331 E2215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr2:169732630 A>G maps to NM_020675.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr2:169732630 A>G maps to NM_020675.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr3:136088079 T>C maps to NM_005862.2 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr3:136088079 T>C maps to NM_005862.2 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr3:170716011 G>A maps to NM_000340.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr3:170716011 G>A maps to NM_000340.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr4:186544866 C>A maps to ENST00000355634 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr4:186544866 C>A maps to ENST00000355634 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:3600732 C>T maps to NM_024337.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:3600732 C>T maps to NM_024337.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:78964812 C>G maps to NM_173797.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:78964812 C>G maps to NM_173797.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:108436172 C>T maps to NM_005246.2 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:108436172 C>T maps to NM_005246.2 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:140710505 C>T maps to NM_018912.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr5:140710505 C>T maps to NM_018912.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:30673686 C>T maps to NM_014641.2 E1091E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:30673686 C>T maps to NM_014641.2 E1091E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:31498939 G>A maps to ENST00000417556 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:31498939 G>A maps to ENST00000417556 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:38649845 G>T maps to NM_006708.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:38649845 G>T maps to NM_006708.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:151116990 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr6:151116990 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr7:122635517 G>A maps to NM_016945.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr7:122635517 G>A maps to NM_016945.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr8:11172555 G>T maps to NM_015458.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr8:11172555 G>T maps to NM_015458.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr10:49667752 G>A maps to ENST00000417912 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr10:49667752 G>A maps to ENST00000417912 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr11:111959636 C>T maps to NM_003002.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr11:111959636 C>T maps to NM_003002.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr11:116692359 G>T maps to NM_000482.3 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr11:116692359 G>T maps to NM_000482.3 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr12:27077407 C>A maps to NM_018164.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr12:27077407 C>A maps to NM_018164.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr13:48985927 A>C maps to NM_005767.5 L211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr13:48985927 A>C maps to NM_005767.5 L211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:41372083 T>A maps to NM_017553.1 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:41372083 T>A maps to NM_017553.1 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:64496767 G>A maps to NM_022048.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:64496767 G>A maps to NM_022048.3 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:87217599 C>T maps to NM_152336.2 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr15:87217599 C>T maps to NM_152336.2 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:20352630 G>A maps to ENST00000424589 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:20352630 G>A maps to ENST00000424589 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:70575581 C>T maps to NM_012426.4 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:70575581 C>T maps to NM_012426.4 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:70884497 G>A maps to NM_032821.2 I4167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr16:70884497 G>A maps to NM_032821.2 I4167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:10448677 G>A maps to NM_017534.5 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:10448677 G>A maps to NM_017534.5 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:17080691 G>A maps to NM_015134.2 E975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:17080691 G>A maps to NM_015134.2 E975E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:17080712 G>A maps to NM_015134.2 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:17080712 G>A maps to NM_015134.2 T982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:78704397 G>A maps to NM_020761.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr17:78704397 G>A maps to NM_020761.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:14307450 C>G maps to NM_198391.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:14307450 C>G maps to NM_198391.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:25405845 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:25405845 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:25666701 C>T maps to NM_015655.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr20:25666701 C>T maps to NM_015655.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr21:45173596 C>T maps to NM_003681.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr21:45173596 C>T maps to NM_003681.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:19839451 C>T maps to NM_024627.5 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:19839451 C>T maps to NM_024627.5 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:38329084 C>G maps to NM_033386.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr22:38329084 C>G maps to NM_033386.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chrX:133512097 G>T maps to ENST00000394292 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chrX:133512097 G>T maps to ENST00000394292 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chrX:152482884 G>A maps to NM_004988.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chrX:152482884 G>A maps to NM_004988.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:1148064 T>C maps to NM_003327.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:1148064 T>C maps to NM_003327.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:19670913 T>C maps to ENST00000375145 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:19670913 T>C maps to ENST00000375145 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:40228855 G>A maps to NM_001720.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:40228855 G>A maps to NM_001720.3 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:169578781 A>G maps to NM_003005.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:169578781 A>G maps to NM_003005.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:180843063 A>G maps to NM_004736.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr1:180843063 A>G maps to NM_004736.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:29258359 G>T maps to NM_199280.2 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:29258359 G>T maps to NM_199280.2 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:55895070 T>C maps to NM_033109.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:55895070 T>C maps to NM_033109.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:159519803 C>T maps to NM_003628.3 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr2:159519803 C>T maps to NM_003628.3 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:4508954 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:4508954 G>C did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr4:37850206 G>A maps to NM_018290.3 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr4:37850206 G>A maps to NM_018290.3 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr4:120107258 T>C maps to NM_016599.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr4:120107258 T>C maps to NM_016599.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr5:37293027 T>C maps to NM_153485.1 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr5:37293027 T>C maps to NM_153485.1 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr5:140024590 C>T maps to ENST00000252100 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr5:140024590 C>T maps to ENST00000252100 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:33284381 G>A maps to NM_001145338.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:33284381 G>A maps to NM_001145338.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:100868686 G>T maps to ENST00000262901 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr6:100868686 G>T maps to ENST00000262901 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr7:22985594 T>C maps to NM_032581.3 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr7:22985594 T>C maps to NM_032581.3 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr8:57026487 C>T maps to NM_005372.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr8:57026487 C>T maps to NM_005372.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:80262685 G>A maps to NM_004297.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:80262685 G>A maps to NM_004297.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:88257813 T>C maps to ENST00000395847 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:88257813 T>C maps to ENST00000395847 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr10:16911659 C>T maps to NM_001081.3 W3143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr10:16911659 C>T maps to NM_001081.3 W3143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr10:135369107 G>T maps to NM_001143764.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr10:135369107 G>T maps to NM_001143764.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:4976304 A>G maps to NM_001004748.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:4976304 A>G maps to NM_001004748.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:15212290 A>G maps to NM_001031853.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:15212290 A>G maps to NM_001031853.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:30033502 C>T maps to NM_002233.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:30033502 C>T maps to NM_002233.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:119170368 C>T maps to NM_005188.2 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr11:119170368 C>T maps to NM_005188.2 Q867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:6554302 C>A maps to NM_001242.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:6554302 C>A maps to NM_001242.4 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:21242856 C>T maps to ENST00000381541 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:21242856 C>T maps to ENST00000381541 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:56720612 A>G maps to NM_001127460.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:56720612 A>G maps to NM_001127460.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:70672039 A>T maps to NM_014515.5 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:70672039 A>T maps to NM_014515.5 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:131487770 C>T maps to NM_198827.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr12:131487770 C>T maps to NM_198827.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr13:38320156 G>A maps to NM_003306.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr13:38320156 G>A maps to NM_003306.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr14:23344693 C>T maps to NM_014045.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr14:23344693 C>T maps to NM_014045.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr16:449377 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr16:449377 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr17:58145063 T>C maps to NM_022070.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr17:58145063 T>C maps to NM_022070.4 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr17:71281970 G>A maps to NM_012121.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr17:71281970 G>A maps to NM_012121.4 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:10475634 G>A maps to NM_003331.4 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:10475634 G>A maps to NM_003331.4 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:41248526 G>A maps to NM_198476.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:41248526 G>A maps to NM_198476.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:42260766 G>A maps to NM_002483.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:42260766 G>A maps to NM_002483.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:46172840 G>A maps to NM_000164.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:46172840 G>A maps to NM_000164.2 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:49797168 G>A maps to NM_014037.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr19:49797168 G>A maps to NM_014037.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr20:30803205 T>C maps to NM_015352.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr20:30803205 T>C maps to NM_015352.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:6173058 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:6173058 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:7907828 G>C maps to NM_006786.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:7907828 G>C maps to NM_006786.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:19595154 C>A maps to NM_201252.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:19595154 C>A maps to NM_201252.3 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:22924701 G>C maps to NM_020526.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:22924701 G>C maps to NM_020526.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:24661178 G>A maps to NM_021180.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:24661178 G>A maps to NM_021180.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:27695778 G>C maps to NM_003665.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:27695778 G>C maps to NM_003665.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:33138429 C>T maps to NM_005610.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:33138429 C>T maps to NM_005610.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:36181307 G>A maps to NM_152374.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:36181307 G>A maps to NM_152374.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:37947424 C>T maps to NM_025079.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:37947424 C>T maps to NM_025079.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:38197173 G>A maps to NM_001099439.1 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:38197173 G>A maps to NM_001099439.1 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:39876600 C>T maps to NM_015038.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:39876600 C>T maps to NM_015038.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:45269323 C>T maps to NM_004073.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:45269323 C>T maps to NM_004073.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:46034628 C>T maps to NM_153326.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:46034628 C>T maps to NM_153326.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:59142622 C>T maps to NM_001085487.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:59142622 C>T maps to NM_001085487.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:67411831 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:67411831 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:84867739 A>G maps to NM_021233.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:84867739 A>G maps to NM_021233.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:99387499 G>A maps to NM_001037317.1 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:99387499 G>A maps to NM_001037317.1 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:110466436 G>A maps to NM_000757.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:110466436 G>A maps to NM_000757.4 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:113234325 G>T maps to NM_020963.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:113234325 G>T maps to NM_020963.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:114524372 G>A maps to NM_020190.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:114524372 G>A maps to NM_020190.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:154000003 G>A maps to NM_207308.2 Q1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:154000003 G>A maps to NM_207308.2 Q1309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:155177628 G>A maps to NM_007112.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:155177628 G>A maps to NM_007112.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:156918211 C>T maps to NM_198236.1 E668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:156918211 C>T maps to NM_198236.1 E668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:169494147 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:169494147 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:197070598 C>T maps to NM_018136.4 Q2594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:197070598 C>T maps to NM_018136.4 Q2594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:202935921 G>C maps to NM_016243.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:202935921 G>C maps to NM_016243.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:204129687 G>C maps to NM_000537.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:204129687 G>C maps to NM_000537.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:207228121 T>C maps to NM_006212.2 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:207228121 T>C maps to NM_006212.2 N20N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:211966440 C>T maps to NM_014873.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:211966440 C>T maps to NM_014873.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:213032135 C>T maps to NM_014053.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:213032135 C>T maps to NM_014053.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:222743963 G>A maps to NM_005681.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:222743963 G>A maps to NM_005681.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:229771853 C>T maps to NM_014777.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:229771853 C>T maps to NM_014777.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:240341298 C>T maps to ENST00000406993 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:240341298 C>T maps to ENST00000406993 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:11765298 C>T maps to NM_014668.3 D1389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:11765298 C>T maps to NM_014668.3 D1389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:20451399 C>T maps to ENST00000361078 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:20451399 C>T maps to ENST00000361078 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:31572631 G>A maps to NM_000379.3 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:31572631 G>A maps to NM_000379.3 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:32289085 G>C maps to NM_014946.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:32289085 G>C maps to NM_014946.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:38893362 G>A maps to NM_138801.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:38893362 G>A maps to NM_138801.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:39042770 G>A maps to NM_198963.1 F1166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:39042770 G>A maps to NM_198963.1 F1166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:43458298 G>A maps to ENST00000330266 Q1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:43458298 G>A maps to ENST00000330266 Q1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:71298937 C>T maps to NM_017567.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:71298937 C>T maps to NM_017567.4 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:74708005 G>A maps to ENST00000393965 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:74708005 G>A maps to ENST00000393965 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:80529639 G>A maps to NM_178839.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:80529639 G>A maps to NM_178839.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:96992596 G>A maps to ENST00000420728 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:96992596 G>A maps to ENST00000420728 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:98263593 G>A maps to NM_001862.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:98263593 G>A maps to NM_001862.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:103236426 G>A maps to NM_003048.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:103236426 G>A maps to NM_003048.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:112733014 G>A maps to NM_006343.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:112733014 G>A maps to NM_006343.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:152127233 T>C maps to NM_004688.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:152127233 T>C maps to NM_004688.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:168106304 C>T maps to NM_152381.5 P2801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:168106304 C>T maps to NM_152381.5 P2801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:198380839 G>A maps to NM_015387.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:198380839 G>A maps to NM_015387.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:208795687 G>A maps to NM_001080475.2 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:208795687 G>A maps to NM_001080475.2 F616F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:219498428 C>T maps to ENST00000432688 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:219498428 C>T maps to ENST00000432688 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:230341867 G>A maps to NM_139072.3 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:230341867 G>A maps to NM_139072.3 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:8809174 G>A maps to NM_000916.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:8809174 G>A maps to NM_000916.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:39139936 C>T maps to NM_031899.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:39139936 C>T maps to NM_031899.2 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:42777312 C>T maps to NM_144719.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:42777312 C>T maps to NM_144719.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:47044730 G>A maps to NM_015175.1 V1884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:47044730 G>A maps to NM_015175.1 V1884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:53159983 G>A maps to NM_052859.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:53159983 G>A maps to NM_052859.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:58109121 C>T maps to NM_001164317.1 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:58109121 C>T maps to NM_001164317.1 L1143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:100354654 A>G maps to NM_032787.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:100354654 A>G maps to NM_032787.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121414424 G>A maps to ENST00000393667 Q1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121414424 G>A maps to ENST00000393667 Q1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121416387 C>T maps to ENST00000393667 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121416387 C>T maps to ENST00000393667 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:124165698 G>A maps to NM_001024660.3 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:124165698 G>A maps to NM_001024660.3 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:129288722 G>A maps to NM_015103.2 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:129288722 G>A maps to NM_015103.2 I1276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:132185189 G>A maps to NM_015268.3 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:132185189 G>A maps to NM_015268.3 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:134967279 G>A maps to NM_004441.4 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:134967279 G>A maps to NM_004441.4 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:155571324 G>A maps to NM_004733.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:155571324 G>A maps to NM_004733.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:159995412 G>A maps to ENST00000483754 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:159995412 G>A maps to ENST00000483754 R799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:195615315 C>T maps to NM_001010938.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:195615315 C>T maps to NM_001010938.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:36212231 G>A maps to NM_015230.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:36212231 G>A maps to NM_015230.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:68934363 G>A maps to NM_207407.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:68934363 G>A maps to NM_207407.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:79238533 C>G maps to NM_025074.6 S611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:79238533 C>G maps to NM_025074.6 S611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:87691108 A>G maps to NM_080685.2 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:87691108 A>G maps to NM_080685.2 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:107249296 G>A maps to NM_001142416.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:107249296 G>A maps to NM_001142416.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:115858491 G>A maps to NM_022569.1 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr4:115858491 G>A maps to NM_022569.1 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:32233925 C>A maps to NM_001040446.1 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:32233925 C>A maps to NM_001040446.1 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:45462007 G>A maps to NM_021072.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:45462007 G>A maps to NM_021072.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:77406124 G>C maps to NM_003664.3 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:77406124 G>C maps to NM_003664.3 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:102442446 T>C maps to NM_017676.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:102442446 T>C maps to NM_017676.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:125968327 C>T maps to NM_207408.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:125968327 C>T maps to NM_207408.1 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:134332198 C>T maps to NM_178019.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:134332198 C>T maps to NM_178019.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:140559207 G>C maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:140559207 G>C maps to NM_019120.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:156932735 A>G maps to ENST00000430702 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:156932735 A>G maps to ENST00000430702 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:160761888 G>T maps to NM_021911.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:160761888 G>T maps to NM_021911.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:167993163 A>G maps to NM_024594.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr5:167993163 A>G maps to NM_024594.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:7581075 G>A maps to NM_004415.2 V1551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:7581075 G>A maps to NM_004415.2 V1551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:18122785 C>A maps to NM_198586.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:18122785 C>A maps to NM_198586.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:26459742 C>T maps to NM_007049.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:26459742 C>T maps to NM_007049.3 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:26501555 C>T maps to NM_001732.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:26501555 C>T maps to NM_001732.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:27107326 G>A maps to NM_003495.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:27107326 G>A maps to NM_003495.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:27833491 G>A maps to NM_003511.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:27833491 G>A maps to NM_003511.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:30681763 C>T maps to NM_014641.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:30681763 C>T maps to NM_014641.2 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:32134564 C>T maps to NM_030652.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:32134564 C>T maps to NM_030652.2 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33283234 G>A maps to NM_001145338.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33283234 G>A maps to NM_001145338.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33284429 G>C maps to NM_001145338.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33284429 G>C maps to NM_001145338.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33385310 G>A maps to NM_001014433.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:33385310 G>A maps to NM_001014433.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:46658619 G>T maps to NM_001010870.2 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:46658619 G>T maps to NM_001010870.2 E919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:51908450 G>A maps to NM_138694.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:51908450 G>A maps to NM_138694.3 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:94068096 G>A maps to NM_004440.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:94068096 G>A maps to NM_004440.3 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:100841696 G>A maps to ENST00000262901 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr6:100841696 G>A maps to ENST00000262901 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:2565140 C>T maps to NM_001040167.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:2565140 C>T maps to NM_001040167.1 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:27797747 C>T maps to ENST00000409980 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:27797747 C>T maps to ENST00000409980 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:44579101 G>A maps to NM_013389.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:44579101 G>A maps to NM_013389.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:107342405 C>G maps to NM_000441.1 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:107342405 C>G maps to NM_000441.1 V646V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:117400555 C>T maps to NM_033427.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:117400555 C>T maps to NM_033427.2 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:150164397 C>T maps to NM_175571.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr7:150164397 C>T maps to NM_175571.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:12947970 C>T maps to NM_182643.2 E1288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:12947970 C>T maps to NM_182643.2 E1288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:19316070 G>T maps to NM_018371.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:19316070 G>T maps to NM_018371.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:21997684 C>T maps to NM_025232.2 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:21997684 C>T maps to NM_025232.2 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:30472222 G>A maps to NM_002095.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:30472222 G>A maps to NM_002095.4 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:61748693 C>T maps to NM_017780.2 Q1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:61748693 C>T maps to NM_017780.2 Q1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:95653663 C>T maps to NM_017697.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:95653663 C>T maps to NM_017697.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:109797207 G>C maps to NM_153015.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:109797207 G>C maps to NM_153015.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:124693584 C>T maps to NM_001003954.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:124693584 C>T maps to NM_001003954.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:139629180 G>A maps to NM_152888.1 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:139629180 G>A maps to NM_152888.1 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:146279412 C>G maps to ENST00000444534 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr8:146279412 C>G maps to ENST00000444534 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:422090 G>A maps to NM_203447.3 K1399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:422090 G>A maps to NM_203447.3 K1399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:429847 C>T maps to NM_203447.3 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:429847 C>T maps to NM_203447.3 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:97082699 G>C maps to NM_017561.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:97082699 G>C maps to NM_017561.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:115598510 G>A maps to NM_001012994.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:115598510 G>A maps to NM_001012994.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:129157917 C>T maps to NM_033446.1 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:129157917 C>T maps to NM_033446.1 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:134454940 C>G maps to NM_198679.1 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:134454940 C>G maps to NM_198679.1 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:135781418 G>A maps to NM_000368.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:135781418 G>A maps to NM_000368.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:137777708 G>A maps to NM_004108.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:137777708 G>A maps to NM_004108.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:137804335 G>C maps to NM_002003.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr9:137804335 G>C maps to NM_002003.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:35317793 G>A maps to NM_001198778.1 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:35317793 G>A maps to NM_001198778.1 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:97376260 G>A maps to NM_002860.3 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:97376260 G>A maps to NM_002860.3 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:101445632 G>A maps to NM_020354.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:101445632 G>A maps to NM_020354.3 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:103900463 G>A maps to NM_015062.3 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:103900463 G>A maps to NM_015062.3 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:103901411 G>A maps to NM_015062.3 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:103901411 G>A maps to NM_015062.3 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:112839121 C>T maps to NM_000681.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:112839121 C>T maps to NM_000681.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:123844345 G>A maps to NM_206862.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:123844345 G>A maps to NM_206862.2 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:135213088 C>T maps to NM_138384.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr10:135213088 C>T maps to NM_138384.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:1025892 G>C maps to NM_005961.2 S904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:1025892 G>C maps to NM_005961.2 S904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:4928820 C>T maps to NM_001004749.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:4928820 C>T maps to NM_001004749.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:5444185 C>G maps to NM_001004757.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:5444185 C>G maps to NM_001004757.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:58978820 G>C maps to NM_001039396.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:58978820 G>C maps to NM_001039396.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:59349007 G>A maps to NM_002556.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:59349007 G>A maps to NM_002556.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:66410997 C>A maps to NM_001198845.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:66410997 C>A maps to NM_001198845.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:116640939 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:116640939 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:118344510 G>A maps to NM_001197104.1 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:118344510 G>A maps to NM_001197104.1 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:120008355 G>C maps to NM_012101.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:120008355 G>C maps to NM_012101.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:124757736 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:124757736 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:124949112 C>T maps to NM_198277.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:124949112 C>T maps to NM_198277.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:129246022 C>G maps to NM_003658.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:129246022 C>G maps to NM_003658.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:130785627 G>A maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr11:130785627 G>A maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:12630831 G>C maps to NM_030640.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:12630831 G>C maps to NM_030640.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:12630909 G>A maps to NM_030640.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:12630909 G>A maps to NM_030640.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:27933976 C>T maps to NM_020782.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:27933976 C>T maps to NM_020782.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:29757223 C>T maps to NM_001193451.1 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:29757223 C>T maps to NM_001193451.1 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:31613258 G>A maps to NM_144973.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:31613258 G>A maps to NM_144973.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:41967406 C>T maps to NM_001164595.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:41967406 C>T maps to NM_001164595.1 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:42854113 C>A maps to NM_153026.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:42854113 C>A maps to NM_153026.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:49890686 C>T maps to NM_023071.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:49890686 C>T maps to NM_023071.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:53647276 C>T maps to NM_001170790.1 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:53647276 C>T maps to NM_001170790.1 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:54423559 C>T maps to NM_004503.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:54423559 C>T maps to NM_004503.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:56334171 C>T maps to NM_201554.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:56334171 C>T maps to NM_201554.1 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:56536447 C>T maps to NM_001184796.1 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:56536447 C>T maps to NM_001184796.1 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:57436894 G>C maps to NM_005379.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:57436894 G>C maps to NM_005379.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:58114291 C>T maps to NM_006812.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:58114291 C>T maps to NM_006812.3 F623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:85547823 T>C maps to NM_001079910.1 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:85547823 T>C maps to NM_001079910.1 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:90005095 G>C maps to ENST00000428670 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:90005095 G>C maps to ENST00000428670 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:94965381 G>A maps to NM_020698.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:94965381 G>A maps to NM_020698.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:102559616 C>T maps to NM_017915.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:102559616 C>T maps to NM_017915.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:105282829 G>A maps to NM_032148.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:105282829 G>A maps to NM_032148.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:112477110 G>T maps to NM_024953.3 Y857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:112477110 G>T maps to NM_024953.3 Y857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:112608963 G>A maps to NM_001109662.2 P3791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:112608963 G>A maps to NM_001109662.2 P3791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:120221777 C>T maps to ENST00000392521 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:120221777 C>T maps to ENST00000392521 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:133428209 G>A maps to NM_001161344.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr12:133428209 G>A maps to NM_001161344.1 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:23904866 G>C maps to NM_014363.4 S4383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:23904866 G>C maps to NM_014363.4 S4383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:37011848 C>T maps to NM_003914.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:37011848 C>T maps to NM_003914.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:111973257 G>A maps to NM_152324.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr13:111973257 G>A maps to NM_152324.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:21780122 G>T maps to NM_020366.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:21780122 G>T maps to NM_020366.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:45542645 C>G maps to ENST00000361462 S1735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:45542645 C>G maps to ENST00000361462 S1735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:51707162 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:51707162 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:75231007 G>A maps to NM_019589.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:75231007 G>A maps to NM_019589.2 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:102514869 C>T maps to NM_001376.4 F4412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:102514869 C>T maps to NM_001376.4 F4412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:104121149 G>A maps to ENST00000445352 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr14:104121149 G>A maps to ENST00000445352 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:42193071 G>C maps to NM_139265.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:42193071 G>C maps to NM_139265.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:52553306 C>T maps to NM_018728.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:52553306 C>T maps to NM_018728.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:68582397 C>T maps to NM_015322.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:68582397 C>T maps to NM_015322.3 V234V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1A3-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DK-A1A3-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:93558042 C>T maps to NM_001271.3 Q1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr15:93558042 C>T maps to NM_001271.3 Q1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:1797073 C>T maps to NM_015133.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:1797073 C>T maps to NM_015133.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:3807964 G>A maps to NM_004380.2 Q1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:3807964 G>A maps to NM_004380.2 Q1152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:30735079 C>T maps to NM_006662.2 T1445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:30735079 C>T maps to NM_006662.2 T1445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:48177900 C>T maps to NM_033226.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:48177900 C>T maps to NM_033226.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50339494 G>A maps to NM_001114.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50339494 G>A maps to NM_001114.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50339738 G>A maps to NM_001114.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50339738 G>A maps to NM_001114.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50383963 G>A maps to NM_001173984.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:50383963 G>A maps to NM_001173984.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:72094455 G>A maps to NM_005143.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:72094455 G>A maps to NM_005143.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:84473070 C>T maps to ENST00000416219 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr16:84473070 C>T maps to ENST00000416219 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:1576683 G>T maps to NM_006445.3 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:1576683 G>T maps to NM_006445.3 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:4086694 G>A maps to NM_016376.3 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:4086694 G>A maps to NM_016376.3 V650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:5462821 G>A maps to NM_033004.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:5462821 G>A maps to NM_033004.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:6930282 G>C maps to NM_181844.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:6930282 G>C maps to NM_181844.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7160257 C>T maps to NM_203414.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7160257 C>T maps to NM_203414.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7217446 G>A maps to NM_004489.4 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7217446 G>A maps to NM_004489.4 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7250444 C>T maps to NM_014716.3 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7250444 C>T maps to NM_014716.3 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:8791858 G>A maps to NM_001142633.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:8791858 G>A maps to NM_001142633.1 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:26856165 C>T maps to NM_003593.2 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:26856165 C>T maps to NM_003593.2 Q252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:39538573 C>T maps to NM_021013.3 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:39538573 C>T maps to NM_021013.3 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:40070072 G>A maps to ENST00000401700 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:40070072 G>A maps to ENST00000401700 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:43196284 C>T maps to NM_133373.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:43196284 C>T maps to NM_133373.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:48434546 G>A maps to NM_022167.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:48434546 G>A maps to NM_022167.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:48460408 G>A maps to NM_018509.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:48460408 G>A maps to NM_018509.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:65141897 T>C maps to NM_014877.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:65141897 T>C maps to NM_014877.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:72929507 C>T maps to NM_178160.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:72929507 C>T maps to NM_178160.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:73017051 G>A maps to NM_001545.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:73017051 G>A maps to NM_001545.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:73839335 G>C maps to ENST00000412096 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:73839335 G>C maps to ENST00000412096 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:74387281 G>A maps to NM_022066.3 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:74387281 G>A maps to NM_022066.3 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr18:47428978 C>A maps to NM_001080467.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr18:47428978 C>A maps to NM_001080467.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr18:51731412 C>T maps to NM_003927.3 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr18:51731412 C>T maps to NM_003927.3 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:2853250 T>A maps to NM_152791.4 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:2853250 T>A maps to NM_152791.4 Y396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:2987902 G>A maps to NM_001143986.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:2987902 G>A maps to NM_001143986.1 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:3984132 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:3984132 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:6177389 C>T maps to NM_030924.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:6177389 C>T maps to NM_030924.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:7083112 C>T maps to NM_024341.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:7083112 C>T maps to NM_024341.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:8136969 G>T maps to NM_032447.3 R2684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:8136969 G>T maps to NM_032447.3 R2684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:9077703 G>A maps to NM_024690.2 Q3248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:9077703 G>A maps to NM_024690.2 Q3248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:12060203 C>T maps to NM_144566.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:12060203 C>T maps to NM_144566.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:16633880 C>T maps to NM_006387.5 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:16633880 C>T maps to NM_006387.5 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17213294 C>G maps to NM_004145.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17213294 C>G maps to NM_004145.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17405303 G>A maps to NM_024527.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17405303 G>A maps to NM_024527.4 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17440785 G>A maps to NM_020959.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:17440785 G>A maps to NM_020959.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:18321949 G>C maps to NM_000923.3 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:18321949 G>C maps to NM_000923.3 S643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:18963839 G>A maps to ENST00000418384 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:18963839 G>A maps to ENST00000418384 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:19612020 G>A maps to ENST00000404158 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:19612020 G>A maps to ENST00000404158 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:34818938 G>A maps to NM_014686.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:34818938 G>A maps to NM_014686.3 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:35758033 C>G maps to NM_205834.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:35758033 C>G maps to NM_205834.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:37382766 G>C maps to NM_001171979.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:37382766 G>C maps to NM_001171979.1 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:40408602 G>C maps to NM_003890.2 A1412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:40408602 G>C maps to NM_003890.2 A1412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:40480724 T>C maps to NM_006503.2 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:40480724 T>C maps to NM_006503.2 H221H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:41884360 C>T maps to NM_001098821.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:41884360 C>T maps to NM_001098821.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:53383881 G>A maps to NM_207333.2 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr19:53383881 G>A maps to NM_207333.2 C499C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:2636003 G>A maps to NM_006392.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:2636003 G>A maps to NM_006392.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:37621004 C>T maps to NM_021931.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:37621004 C>T maps to NM_021931.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:40065974 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:40065974 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:43243232 C>T maps to NM_181805.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:43243232 C>T maps to NM_181805.1 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:47704591 C>T maps to NM_001316.2 Y590Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:47704591 C>T maps to NM_001316.2 Y590Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:48503323 C>T maps to ENST00000417961 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:48503323 C>T maps to ENST00000417961 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:51871959 G>T maps to NM_173485.5 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:51871959 G>T maps to NM_173485.5 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:62195446 C>T maps to NM_001037335.2 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:62195446 C>T maps to NM_001037335.2 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:62838959 C>G maps to NM_004535.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr20:62838959 C>G maps to NM_004535.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:22161969 G>A maps to NM_138957.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:22161969 G>A maps to NM_138957.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:36681273 G>A maps to NM_002473.4 V1792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:36681273 G>A maps to NM_002473.4 V1792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:46932098 C>T maps to NM_014246.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:46932098 C>T maps to NM_014246.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:50928200 C>T maps to NM_017584.5 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr22:50928200 C>T maps to NM_017584.5 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chrX:1475112 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chrX:1475112 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chrX:27840055 C>T maps to NM_182506.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chrX:27840055 C>T maps to NM_182506.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chrX:153697281 C>T maps to NM_017514.3 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chrX:153697281 C>T maps to NM_017514.3 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:6697332 C>A maps to NM_018198.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:6697332 C>A maps to NM_018198.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:22828865 C>T maps to NM_014870.3 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:22828865 C>T maps to NM_014870.3 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:34329949 C>G maps to NM_145205.4 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:34329949 C>G maps to NM_145205.4 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:50610765 C>T maps to NM_021952.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:50610765 C>T maps to NM_021952.3 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:52863535 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:52863535 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:54060248 C>T maps to NM_147193.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:54060248 C>T maps to NM_147193.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:55523841 C>G maps to NM_174936.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:55523841 C>G maps to NM_174936.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:94476480 C>T maps to NM_000350.2 E1863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:94476480 C>T maps to NM_000350.2 E1863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:94674862 G>A maps to NM_004815.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:94674862 G>A maps to NM_004815.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:145586853 G>A maps to NM_001012758.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:145586853 G>A maps to NM_001012758.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:149885326 G>T maps to NM_014849.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:149885326 G>T maps to NM_014849.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:155020371 C>G maps to NM_152494.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:155020371 C>G maps to NM_152494.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:202571538 C>T maps to NM_177402.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:202571538 C>T maps to NM_177402.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:238048518 G>A maps to NM_021186.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:238048518 G>A maps to NM_021186.3 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:247200918 C>A maps to NM_033213.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:247200918 C>A maps to NM_033213.3 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:248685405 C>T maps to NM_001013355.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr1:248685405 C>T maps to NM_001013355.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:11773123 G>A maps to NM_014668.3 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:11773123 G>A maps to NM_014668.3 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:97216889 C>T maps to NM_212481.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:97216889 C>T maps to NM_212481.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:219679422 C>G maps to NM_000784.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:219679422 C>G maps to NM_000784.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:220439959 C>T maps to NM_002191.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:220439959 C>T maps to NM_002191.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:220466158 C>G maps to NM_052902.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr2:220466158 C>G maps to NM_052902.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:9965626 G>T maps to NM_153461.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:9965626 G>T maps to NM_153461.2 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:17053636 G>A maps to NM_001144382.1 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:17053636 G>A maps to NM_001144382.1 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:36872832 G>C maps to NM_014831.2 V2703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:36872832 G>C maps to NM_014831.2 V2703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:37376608 G>A maps to NM_001172713.1 K2108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:37376608 G>A maps to NM_001172713.1 K2108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:40457434 G>A maps to NM_001248.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:40457434 G>A maps to NM_001248.2 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:154139249 G>A maps to NM_001038705.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:154139249 G>A maps to NM_001038705.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:160156350 G>A maps to ENST00000483754 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr3:160156350 G>A maps to ENST00000483754 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:7985050 G>C maps to NM_001130083.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:7985050 G>C maps to NM_001130083.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:22449099 G>A maps to NM_145290.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:22449099 G>A maps to NM_145290.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:73013406 C>T maps to NM_004885.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:73013406 C>T maps to NM_004885.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:126337751 C>A maps to NM_024582.4 V2331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr4:126337751 C>A maps to NM_024582.4 V2331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:34043212 G>T maps to NM_181435.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:34043212 G>T maps to NM_181435.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:150666827 C>T maps to NM_001145017.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:150666827 C>T maps to NM_001145017.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:151179851 C>T maps to NM_198395.1 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr5:151179851 C>T maps to NM_198395.1 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:7231958 C>T maps to NM_001003699.3 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:7231958 C>T maps to NM_001003699.3 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:38810630 T>C maps to ENST00000327475 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:38810630 T>C maps to ENST00000327475 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:46214587 G>C maps to ENST00000405162 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:46214587 G>C maps to ENST00000405162 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:117746801 A>G maps to NM_002944.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr6:117746801 A>G maps to NM_002944.2 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:72721625 C>T maps to NM_148956.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:72721625 C>T maps to NM_148956.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:75048153 G>C maps to ENST00000257665 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:75048153 G>C maps to ENST00000257665 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:81388060 G>C maps to NM_000601.4 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:81388060 G>C maps to NM_000601.4 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:96747139 G>A maps to NM_020186.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:96747139 G>A maps to NM_020186.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:99710523 C>T maps to ENST00000472509 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:99710523 C>T maps to ENST00000472509 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:135261758 G>C maps to NM_015135.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:135261758 G>C maps to NM_015135.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:135263631 G>A maps to NM_015135.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:135263631 G>A maps to NM_015135.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:148769074 C>T maps to NM_152411.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:148769074 C>T maps to NM_152411.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:150390121 C>T maps to NM_015660.2 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr7:150390121 C>T maps to NM_015660.2 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:22442666 C>T maps to NM_021630.5 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:22442666 C>T maps to NM_021630.5 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:125568499 C>T maps to NM_014751.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:125568499 C>T maps to NM_014751.4 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:145806414 C>T maps to NM_025251.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr8:145806414 C>T maps to NM_025251.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:74764525 C>T maps to ENST00000238018 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:74764525 C>T maps to ENST00000238018 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:136804248 G>T maps to NM_001134398.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:136804248 G>T maps to NM_001134398.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:140707936 C>T maps to NM_024757.4 C1045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr9:140707936 C>T maps to NM_024757.4 C1045C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:5988887 G>C maps to NM_001146033.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:5988887 G>C maps to NM_001146033.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:48511050 C>G maps to NM_001005512.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:48511050 C>G maps to NM_001005512.2 S236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:49176029 G>A maps to NM_004476.1 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:49176029 G>A maps to NM_004476.1 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:57193531 C>T maps to ENST00000428603 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:57193531 C>T maps to ENST00000428603 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:59224918 G>A maps to NM_001004708.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:59224918 G>A maps to NM_001004708.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:64708118 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:64708118 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:89424063 C>T maps to NM_153696.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:89424063 C>T maps to NM_153696.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:7556185 A>G maps to ENST00000416109 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:7556185 A>G maps to ENST00000416109 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:26875356 G>A maps to NM_002223.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:26875356 G>A maps to NM_002223.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:55688665 G>A maps to NM_001005493.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:55688665 G>A maps to NM_001005493.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:71833916 G>A maps to NM_003667.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:71833916 G>A maps to NM_003667.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:108011967 G>A maps to NM_001018072.1 E755E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:108011967 G>A maps to NM_001018072.1 E755E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:120263154 C>T maps to ENST00000392521 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr12:120263154 C>T maps to ENST00000392521 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr13:28589745 C>T maps to NM_004119.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr13:28589745 C>T maps to NM_004119.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:31614066 G>C maps to NM_015382.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:31614066 G>C maps to NM_015382.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:58949407 C>G maps to ENST00000354386 S1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:58949407 C>G maps to ENST00000354386 S1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:63269242 C>G maps to NM_139318.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:63269242 C>G maps to NM_139318.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:64586260 G>A maps to NM_182914.2 L4319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:64586260 G>A maps to NM_182914.2 L4319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:68043122 C>G maps to NM_020715.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr14:68043122 C>G maps to NM_020715.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr15:59502739 G>A maps to NM_004998.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr15:59502739 G>A maps to NM_004998.2 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr15:85401088 C>T maps to NM_020778.4 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr15:85401088 C>T maps to NM_020778.4 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:20410610 G>A maps to NM_174924.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:20410610 G>A maps to NM_174924.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:20430711 C>G maps to NM_017888.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:20430711 C>G maps to NM_017888.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:66584021 G>C maps to ENST00000299697 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:66584021 G>C maps to ENST00000299697 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:72923774 G>C maps to NM_006885.3 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr16:72923774 G>C maps to NM_006885.3 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:16285787 C>T maps to NM_018955.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:16285787 C>T maps to NM_018955.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:18498090 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:18498090 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:61611503 C>T maps to NM_030779.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:61611503 C>T maps to NM_030779.2 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:67178945 G>C maps to NM_080282.3 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:67178945 G>C maps to NM_080282.3 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:79164796 C>G maps to ENST00000269392 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:79164796 C>G maps to ENST00000269392 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:79165120 C>T maps to ENST00000269392 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr17:79165120 C>T maps to ENST00000269392 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr18:33722263 C>G maps to ENST00000442325 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr18:33722263 C>G maps to ENST00000442325 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:1811503 C>A maps to NM_138813.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:1811503 C>A maps to NM_138813.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:9067795 C>T maps to NM_024690.2 V6550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:9067795 C>T maps to NM_024690.2 V6550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:11123725 C>T maps to NM_001128849.1 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:11123725 C>T maps to NM_001128849.1 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:16001183 G>A maps to NM_001082.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:16001183 G>A maps to NM_001082.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:39421109 G>A maps to NM_017827.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:39421109 G>A maps to NM_017827.3 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:49558232 G>A maps to ENST00000377280 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:49558232 G>A maps to ENST00000377280 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:53303273 C>T maps to NM_006969.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr19:53303273 C>T maps to NM_006969.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:31805356 C>T maps to NM_178466.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:31805356 C>T maps to NM_178466.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:35521385 G>A maps to NM_015474.3 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:35521385 G>A maps to NM_015474.3 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:50049279 C>T maps to NM_012340.3 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:50049279 C>T maps to NM_012340.3 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:55027047 C>G maps to NM_020356.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:55027047 C>G maps to NM_020356.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:62324318 C>G maps to ENST00000482936 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr20:62324318 C>G maps to ENST00000482936 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr21:36079651 C>T maps to ENST00000360731 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr21:36079651 C>T maps to ENST00000360731 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:24236666 G>A maps to NM_002415.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:24236666 G>A maps to NM_002415.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:32480978 C>T maps to NM_000343.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:32480978 C>T maps to NM_000343.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:32924938 C>T maps to NM_003490.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:32924938 C>T maps to NM_003490.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:36624295 C>G maps to ENST00000451256 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr22:36624295 C>G maps to ENST00000451256 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chrX:19947929 G>A maps to ENST00000379682 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chrX:19947929 G>A maps to ENST00000379682 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chrX:54841755 G>T maps to NM_201222.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chrX:54841755 G>T maps to NM_201222.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chrX:99663457 C>T maps to NM_001184880.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chrX:99663457 C>T maps to NM_001184880.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:19449356 G>C maps to ENST00000375267 S3262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:19449356 G>C maps to ENST00000375267 S3262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:27277224 C>T maps to NM_152365.2 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:27277224 C>T maps to NM_152365.2 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:36941191 C>T maps to NM_156039.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:36941191 C>T maps to NM_156039.3 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:94650458 G>T maps to NM_004815.3 S693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:94650458 G>T maps to NM_004815.3 S693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:159842831 C>G maps to NM_012337.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:159842831 C>G maps to NM_012337.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:169677939 G>A maps to NM_000655.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:169677939 G>A maps to NM_000655.4 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:203667471 A>G maps to NM_001001396.1 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr1:203667471 A>G maps to NM_001001396.1 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:8919857 G>A maps to NM_020738.2 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:8919857 G>A maps to NM_020738.2 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:11367378 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:11367378 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:171700563 T>A maps to NM_000817.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:171700563 T>A maps to NM_000817.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:179566961 C>T maps to NM_133378.4 S8904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr2:179566961 C>T maps to NM_133378.4 S8904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:47125298 C>A maps to NM_014159.6 E1991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:47125298 C>A maps to NM_014159.6 E1991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:49051673 C>T maps to NM_018031.3 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:49051673 C>T maps to NM_018031.3 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:121994735 G>C maps to NM_001178065.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:121994735 G>C maps to NM_001178065.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:123046524 G>A maps to NM_183357.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:123046524 G>A maps to NM_183357.2 N629N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:136287646 C>T maps to NM_005862.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:136287646 C>T maps to NM_005862.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:141671501 G>C maps to NM_001178139.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:141671501 G>C maps to NM_001178139.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:151046555 A>G maps to NM_176894.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr3:151046555 A>G maps to NM_176894.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:9784900 C>T maps to NM_000798.4 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:9784900 C>T maps to NM_000798.4 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:56471507 A>C maps to NM_006681.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:56471507 A>C maps to NM_006681.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:134071561 C>A maps to NM_032961.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:134071561 C>A maps to NM_032961.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:144127184 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:144127184 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:169167597 C>A maps to NM_017631.5 G1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr4:169167597 C>A maps to NM_017631.5 G1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:115833064 A>T maps to ENST00000257414 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:115833064 A>T maps to ENST00000257414 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:138654643 T>C maps to ENST00000394800 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:138654643 T>C maps to ENST00000394800 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:177637273 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr5:177637273 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:31919362 G>A maps to ENST00000437789 K1209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:31919362 G>A maps to ENST00000437789 K1209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:32808758 G>A maps to NM_148919.3 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:32808758 G>A maps to NM_148919.3 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:32945995 C>A maps to ENST00000395289 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:32945995 C>A maps to ENST00000395289 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:33245679 G>T maps to NM_003782.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:33245679 G>T maps to NM_003782.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:41621153 G>C maps to NM_005586.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:41621153 G>C maps to NM_005586.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:87970339 C>G maps to NM_015021.1 P2331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:87970339 C>G maps to NM_015021.1 P2331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:137325793 A>G maps to NM_014432.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:137325793 A>G maps to NM_014432.2 Y276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:160483634 C>G maps to NM_000876.2 P1218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr6:160483634 C>G maps to NM_000876.2 P1218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:4171954 A>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:4171954 A>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:6210830 A>C did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:6210830 A>C did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:121650515 G>A maps to NM_002851.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:121650515 G>A maps to NM_002851.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:133884159 G>A maps to NM_144648.1 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:133884159 G>A maps to NM_144648.1 E578E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:144320257 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr7:144320257 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:19818561 G>A maps to NM_000237.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:19818561 G>A maps to NM_000237.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:67089286 G>A maps to NM_000756.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr8:67089286 G>A maps to NM_000756.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr9:131329129 T>C maps to NM_001130438.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr9:131329129 T>C maps to NM_001130438.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:15058949 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:15058949 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:75406721 C>T maps to NM_001114133.1 Q896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:75406721 C>T maps to NM_001114133.1 Q896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:120817658 G>A maps to NM_003750.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:120817658 G>A maps to NM_003750.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:134018388 C>T maps to NM_006426.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:134018388 C>T maps to NM_006426.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:135011910 C>T maps to ENST00000368572 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr10:135011910 C>T maps to ENST00000368572 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr11:6129403 C>T maps to NM_001005181.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr11:6129403 C>T maps to NM_001005181.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr11:102495963 G>C maps to NM_004771.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr11:102495963 G>C maps to NM_004771.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:55863094 A>G maps to NM_001005499.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:55863094 A>G maps to NM_001005499.1 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:72680476 C>T maps to NM_013381.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:72680476 C>T maps to NM_013381.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:111758092 G>T maps to NM_015267.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr12:111758092 G>T maps to NM_015267.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:25043946 C>T maps to NM_001911.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:25043946 C>T maps to NM_001911.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:65197534 G>T maps to ENST00000394691 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:65197534 G>T maps to ENST00000394691 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:91356956 C>T maps to NM_004755.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr14:91356956 C>T maps to NM_004755.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:28467359 G>A maps to NM_004667.4 G1822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:28467359 G>A maps to NM_004667.4 G1822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:48752455 G>C maps to NM_000138.4 T1761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:48752455 G>C maps to NM_000138.4 T1761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:76994115 G>A maps to ENST00000324767 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr15:76994115 G>A maps to ENST00000324767 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr16:23700963 C>T maps to NM_005030.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr16:23700963 C>T maps to NM_005030.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr16:74685991 G>A maps to NM_018124.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr16:74685991 G>A maps to NM_018124.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr17:17394773 A>T maps to NM_018019.2 K136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr17:17394773 A>T maps to NM_018019.2 K136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr17:56774140 T>C maps to NM_058216.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr17:56774140 T>C maps to NM_058216.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr18:22806432 G>A maps to NM_015461.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr18:22806432 G>A maps to NM_015461.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr18:31318936 A>G maps to NM_030632.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr18:31318936 A>G maps to NM_030632.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:4236931 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:4236931 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:33663288 T>C maps to NM_173479.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:33663288 T>C maps to NM_173479.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:56733065 C>A maps to NM_024303.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr19:56733065 C>A maps to NM_024303.1 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr20:47888255 A>G maps to NM_021035.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr20:47888255 A>G maps to NM_021035.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr20:60883122 C>T maps to NM_175573.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr20:60883122 C>T maps to NM_175573.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr21:34994368 C>T maps to ENST00000416217 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr21:34994368 C>T maps to ENST00000416217 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:36697581 G>A maps to NM_002473.4 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:36697581 G>A maps to NM_002473.4 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:41928096 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:41928096 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:41980551 G>A maps to NM_002676.2 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:41980551 G>A maps to NM_002676.2 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:50563823 C>T maps to NM_018995.2 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chr22:50563823 C>T maps to NM_018995.2 L525L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-A1A7-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-DK-A1A7-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chrX:65242173 G>A maps to NM_007268.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chrX:65242173 G>A maps to NM_007268.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chrX:135428140 T>G maps to NM_153834.3 L759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A7-01A-11D-A13W-08 chrX:135428140 T>G maps to NM_153834.3 L759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:68512368 G>A maps to NM_004675.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:68512368 G>A maps to NM_004675.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:100732129 C>T maps to NM_001130841.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:100732129 C>T maps to NM_001130841.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:151491774 C>T maps to NM_020770.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:151491774 C>T maps to NM_020770.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:155629591 C>T maps to ENST00000368339 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:155629591 C>T maps to ENST00000368339 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:168014276 G>A maps to ENST00000367840 Q690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:168014276 G>A maps to ENST00000367840 Q690Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773837 C>T maps to NM_014777.2 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773837 C>T maps to NM_014777.2 Q1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773863 C>T maps to NM_014777.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773863 C>T maps to NM_014777.2 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:242048725 G>A maps to NM_006027.4 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:242048725 G>A maps to NM_006027.4 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:8931354 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:8931354 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:11798718 G>A maps to NM_012344.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:11798718 G>A maps to NM_012344.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:49244634 G>A maps to NM_000145.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:49244634 G>A maps to NM_000145.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:54874296 G>A maps to NM_003128.2 K1632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:54874296 G>A maps to NM_003128.2 K1632K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:74779554 G>A maps to NM_032603.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:74779554 G>A maps to NM_032603.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:102460599 C>A maps to NM_145686.2 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:102460599 C>A maps to NM_145686.2 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:118582551 C>T maps to NM_006773.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:118582551 C>T maps to NM_006773.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:120194517 C>T maps to NM_183240.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:120194517 C>T maps to NM_183240.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:179481948 C>A maps to NM_133378.4 E13357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:179481948 C>A maps to NM_133378.4 E13357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:196636428 C>T maps to NM_018897.2 L3796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr2:196636428 C>T maps to NM_018897.2 L3796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:47142946 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:47142946 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:62261594 G>A maps to NM_002841.3 Q1171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:62261594 G>A maps to NM_002841.3 Q1171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:73114034 C>G maps to NM_174907.2 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:73114034 C>G maps to NM_174907.2 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:73114240 C>A maps to NM_174907.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:73114240 C>A maps to NM_174907.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:127295477 C>T maps to NM_001136053.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:127295477 C>T maps to NM_001136053.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:134920359 C>G maps to NM_004441.4 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:134920359 C>G maps to NM_004441.4 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:136045669 G>C maps to NM_001178014.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr3:136045669 G>C maps to NM_001178014.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:6087326 C>G maps to NM_001099433.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:6087326 C>G maps to NM_001099433.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:10083019 G>A maps to NM_017491.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:10083019 G>A maps to NM_017491.3 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:47593106 G>C maps to NM_020453.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:47593106 G>C maps to NM_020453.3 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:68619663 G>A maps to NM_000406.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:68619663 G>A maps to NM_000406.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:109004528 G>A maps to NM_016269.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr4:109004528 G>A maps to NM_016269.4 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr5:7817055 C>T maps to NM_020546.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr5:7817055 C>T maps to NM_020546.2 I987I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr5:179318450 G>A maps to NM_198868.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr5:179318450 G>A maps to NM_198868.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:27839871 C>T maps to NM_003533.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:27839871 C>T maps to NM_003533.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:31616999 G>A maps to ENST00000404765 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:31616999 G>A maps to ENST00000404765 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:32017874 G>A maps to ENST00000375244 V3113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr6:32017874 G>A maps to ENST00000375244 V3113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr7:14733764 G>A maps to NM_004080.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr7:14733764 G>A maps to NM_004080.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr7:17378910 G>T maps to NM_001621.4 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr7:17378910 G>T maps to NM_001621.4 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:35406936 G>A maps to ENST00000416672 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:35406936 G>A maps to ENST00000416672 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:59494244 G>C maps to NM_005625.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:59494244 G>C maps to NM_005625.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:77764239 C>T maps to NM_024721.4 Q1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:77764239 C>T maps to NM_024721.4 Q1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:100904265 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:100904265 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:107763045 G>A maps to NM_001198533.1 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:107763045 G>A maps to NM_001198533.1 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:113348980 G>A maps to NM_198123.1 Q2307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr8:113348980 G>A maps to NM_198123.1 Q2307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr9:104309796 G>A maps to NM_019592.5 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr9:104309796 G>A maps to NM_019592.5 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr9:133780648 G>C maps to NM_001145106.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr9:133780648 G>C maps to NM_001145106.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:3197792 G>T maps to ENST00000380989 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:3197792 G>T maps to ENST00000380989 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:27459816 G>A maps to NM_001172303.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:27459816 G>A maps to NM_001172303.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:44112075 G>A maps to NM_145312.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:44112075 G>A maps to NM_145312.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:92617281 C>G maps to NM_019859.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:92617281 C>G maps to NM_019859.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:106209908 C>G maps to NM_001008723.1 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr10:106209908 C>G maps to NM_001008723.1 L819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:18451305 C>A maps to NM_017448.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:18451305 C>A maps to NM_017448.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:19955346 G>A maps to ENST00000396087 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:19955346 G>A maps to ENST00000396087 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:59245788 C>G maps to NM_001004705.1 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:59245788 C>G maps to NM_001004705.1 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:61254052 C>T maps to NM_145017.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:61254052 C>T maps to NM_145017.2 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:70507824 C>T maps to NM_133266.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:70507824 C>T maps to NM_133266.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:72145374 C>G maps to NM_030813.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr11:72145374 C>G maps to NM_030813.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:27067368 G>T maps to NM_018164.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:27067368 G>T maps to NM_018164.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:27573405 G>T maps to NM_020183.3 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:27573405 G>T maps to NM_020183.3 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:30833507 G>A maps to NM_006390.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:30833507 G>A maps to NM_006390.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:49230567 G>A maps to NM_004818.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:49230567 G>A maps to NM_004818.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:51759232 G>A maps to NM_007210.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:51759232 G>A maps to NM_007210.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:52163722 G>T maps to NM_014191.2 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:52163722 G>T maps to NM_014191.2 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:109654664 G>T maps to NM_001093.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:109654664 G>T maps to NM_001093.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:120652696 G>T maps to NM_001080855.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr12:120652696 G>T maps to NM_001080855.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr13:113532598 G>C maps to NM_015205.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr13:113532598 G>C maps to NM_015205.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:39627490 G>A maps to NM_001079537.1 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:39627490 G>A maps to NM_001079537.1 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:39783994 C>T maps to ENST00000396158 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:39783994 C>T maps to ENST00000396158 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:50074212 G>A maps to NM_152329.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:50074212 G>A maps to NM_152329.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:50472343 G>C maps to NM_001012706.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:50472343 G>C maps to NM_001012706.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:64727308 G>A maps to NM_001437.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:64727308 G>A maps to NM_001437.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:102442047 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr14:102442047 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:22933810 C>T maps to NM_014608.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:22933810 C>T maps to NM_014608.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:29393869 G>A maps to NM_005503.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:29393869 G>A maps to NM_005503.3 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:43932620 C>T maps to NM_172095.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr15:43932620 C>T maps to NM_172095.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:19085284 G>T maps to NM_016138.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:19085284 G>T maps to NM_016138.4 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:57508775 G>A maps to NM_018110.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:57508775 G>A maps to NM_018110.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:72992823 G>A maps to NM_006885.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:72992823 G>A maps to NM_006885.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:3494636 G>A maps to ENST00000399756 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:3494636 G>A maps to ENST00000399756 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:7080604 G>A maps to NM_001671.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:7080604 G>A maps to NM_001671.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:38991463 C>T maps to NM_001195386.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:38991463 C>T maps to NM_001195386.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:62020201 G>A maps to NM_000334.4 V1424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:62020201 G>A maps to NM_000334.4 V1424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:78188481 G>C maps to NM_000199.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr17:78188481 G>C maps to NM_000199.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:14516630 C>T maps to NM_078481.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:14516630 C>T maps to NM_078481.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:39001343 C>G maps to NM_000540.2 L3015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:39001343 C>G maps to NM_000540.2 L3015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:42848851 C>G maps to ENST00000251268 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:42848851 C>G maps to ENST00000251268 S655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:43026091 G>A maps to NM_001712.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:43026091 G>A maps to NM_001712.4 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:45285643 C>G maps to NM_012116.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:45285643 C>G maps to NM_012116.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:50387618 C>T maps to NM_024682.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:50387618 C>T maps to NM_024682.2 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:51361377 C>G maps to NM_001648.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr19:51361377 C>G maps to NM_001648.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr20:43030113 G>A maps to ENST00000338692 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr20:43030113 G>A maps to ENST00000338692 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr20:56728656 G>A maps to NM_178456.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr20:56728656 G>A maps to NM_178456.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chrX:44969326 G>T maps to NM_021140.2 E1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chrX:44969326 G>T maps to NM_021140.2 E1337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chrX:109696040 C>A maps to NM_020769.2 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chrX:109696040 C>A maps to NM_020769.2 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chrX:139865961 G>A maps to NM_004065.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chrX:139865961 G>A maps to NM_004065.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr10:17813343 A>G maps to NM_001098844.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr10:17813343 A>G maps to NM_001098844.1 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:54306930 C>T maps to ENST00000260323 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A0C8-01A-11D-A10S-08 chr15:54306930 C>T maps to ENST00000260323 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:115079343 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr1:115079343 C>T did not map to a codon.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:45655521 G>A maps to NM_198478.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A0YX-01A-11D-A10S-08 chr19:45655521 G>A maps to NM_198478.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:70308613 C>T maps to NM_004536.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20T-01A-11D-A14W-08 chr5:70308613 C>T maps to NM_004536.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr21:10998298 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr21:10998298 G>C did not map to a codon.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:151860061 G>A maps to ENST00000355193 Q3534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F1-01A-11D-A10S-08 chr7:151860061 G>A maps to ENST00000355193 Q3534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:24801247 C>T maps to NM_003102.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C4-A0F6-01A-11D-A10S-08 chr4:24801247 C>T maps to NM_003102.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:18112245 C>G maps to NM_002438.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr10:18112245 C>G maps to NM_002438.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:49027247 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YN-01A-21D-A10S-08 chr13:49027247 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:13001217 G>C maps to ENST00000415464 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YO-01A-11D-A10S-08 chr1:13001217 G>C maps to ENST00000415464 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:201185732 G>A maps to NM_001164586.1 L3149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr1:201185732 G>A maps to NM_001164586.1 L3149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:43801741 G>A maps to ENST00000330266 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr2:43801741 G>A maps to ENST00000330266 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121416257 C>A maps to ENST00000393667 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr3:121416257 C>A maps to ENST00000393667 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7217706 C>A maps to NM_004489.4 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A3-01A-11D-A13W-08 chr17:7217706 C>A maps to NM_004489.4 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:63129870 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1A5-01A-11D-A13W-08 chr11:63129870 C>A did not map to a codon.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773885 C>T maps to NM_014777.2 Q1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr1:229773885 C>T maps to NM_014777.2 Q1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:30910756 C>G maps to NM_001330.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AB-01A-11D-A13W-08 chr16:30910756 C>G maps to NM_001330.3 S16*. Only missense variants will be evaluated by CHASM.
