6105 NP_705833 Q322K not found in SNVbox database
9003 NP_705833 M529I not found in SNVbox database
9696 NP_001070868 E536K not found in SNVbox database
1280 NP_001070868 L111F not found in SNVbox database
1691 NP_705833 L179V not found in SNVbox database
1855 NP_001070868 D124H not found in SNVbox database
3213 NP_705833 G857V not found in SNVbox database
4042 NP_001070868 F327S not found in SNVbox database
4201 NP_705833 I892M not found in SNVbox database
4284 NP_001070868 Y203H not found in SNVbox database
4489 NP_001070868 Q348K not found in SNVbox database
4947 NP_705833 P422T 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 chr1:145534099 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 chr1:156281972 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 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 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 chr13:23929790 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 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 chr14:74194192 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 chr15:54306222 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 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 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 chr17:40837382 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 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 chr2:200137184 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 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 chr20:62724216 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 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 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 chr3:50231194 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 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 chr4:164534482 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 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 chr5:121786335 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 chr5:134041066 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 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 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 chr7:120740099 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 chr8:95674783 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 chr9:136211044 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 chr9:140109623 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 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 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 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 chr12:124416628 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 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 chr16:84684520 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 chr17:42937867 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 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 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 chr19:51958720 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 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 chr2:219884301 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 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 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 chr5:101592817 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 chr6:43305864 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 chr6:157517417 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 chr7:25264764 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 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 chr1:211276925 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 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 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 chr11:62289474 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 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 chr12:124109398 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 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 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 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 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 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 chr19:44891095 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 chr19:55493696 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 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 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 chr20:36758656 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 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 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 chr3:57827024 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 chr4:83776176 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 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 chr5:140167230 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 chr6:166571979 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 chr7:133812299 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 chr8:36793050 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-A3JM-01A-12D-A21A-08 chr1:1325720 C>A maps to NM_030937.4 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:23768755 G>C maps to NM_017707.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:27105792 G>T maps to NM_006015.4 E1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:33490111 C>T maps to NM_001625.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:43232528 G>C maps to NM_022356.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:117529498 C>T maps to NM_020440.2 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:166973534 C>T maps to NM_032858.1 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:179989147 C>T maps to NM_014810.4 Q747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:180063621 G>A maps to NM_014810.4 K2794K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BL-A3JM-01A-12D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr1:228400371 C>G maps to ENST00000337335 *159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr10:21804749 C>A maps to NM_207371.3 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr10:102045869 C>T maps to NM_173809.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:17409116 G>T maps to NM_000525.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:36595000 G>A maps to NM_000448.2 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:55587568 C>A maps to ENST00000395203 S157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:58893254 G>A maps to NM_198947.3 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:60777200 G>A maps to NM_006725.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:68174202 C>T maps to NM_002335.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:70028636 C>T maps to NM_018043.5 F811F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:117866302 G>T did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr11:128844062 G>C maps to NM_001142685.1 S996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:22059096 A>G maps to NM_005691.2 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:50189000 G>C maps to NM_001037806.3 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:51707618 G>A maps to NM_016293.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:53215787 C>G maps to NM_175834.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:57861868 C>T maps to NM_005269.2 D390D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:85450508 A>G maps to NM_001079910.1 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr12:124345627 C>T maps to NM_207437.3 I2155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:37563686 A>G maps to NM_013338.4 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:72440380 G>C maps to ENST00000359684 S176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr13:103445989 C>T maps to NM_024089.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr14:102461423 G>A maps to NM_001376.4 Q1145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr16:31144120 G>A maps to NM_002773.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:5257703 A>G maps to NM_004703.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:7906988 G>A maps to NM_000180.3 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:10364371 C>G did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:10409365 A>G maps to NM_005963.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr17:66913592 C>T did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr18:65180300 C>T maps to NM_032160.2 W525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:6731900 C>T did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:7833780 G>A maps to NM_014257.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:9213856 C>T maps to NM_001005193.1 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:17892530 G>A maps to NM_015122.2 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:31039639 A>G maps to NM_014717.1 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:40909667 G>A maps to NM_181882.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:46997597 G>A maps to NM_020709.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:47124611 G>A maps to NM_000960.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr19:59069643 C>T maps to NM_003969.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr2:44101117 C>T maps to NM_022437.2 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr2:88425823 C>A maps to NM_001443.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr2:233245161 C>G maps to NM_001632.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr20:43727082 G>A maps to NM_002251.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr20:60712443 G>A maps to NM_002792.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr22:32275582 G>A maps to NM_001136029.1 W1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:11851123 C>T maps to ENST00000444133 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:52256621 G>A maps to ENST00000494383 F723F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:58062848 C>T maps to NM_001164317.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:97806240 T>G maps to NM_054106.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:185766490 G>A maps to NM_004454.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr3:194147856 A>C maps to NM_024524.3 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:23815313 T>G maps to NM_013261.3 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:40440103 G>A maps to NM_001098634.1 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:55564534 A>T maps to NM_000222.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr4:88534105 C>T maps to NM_014208.3 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr5:54410096 C>T maps to NM_001170402.1 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr5:150406999 C>T maps to NM_002084.3 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:32944129 C>T maps to ENST00000395289 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:39047366 C>A maps to NM_002062.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:41708251 G>C maps to NM_002630.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:42016404 C>T did not map to a codon.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:43400683 C>T maps to NM_033450.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:52698950 A>C maps to NM_153699.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:146720832 C>T maps to NM_000838.3 A886A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:160225084 C>T maps to NM_173516.1 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr6:167550263 T>G maps to NM_004367.5 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr7:83636799 C>A maps to NM_006080.2 G337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr7:147600708 C>T maps to NM_014141.5 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr8:1841802 G>A maps to ENST00000398564 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr8:96166421 C>G maps to NM_024613.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr8:113318248 G>T maps to NM_198123.1 T2686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:32986022 G>A maps to NM_001195248.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:130210619 G>C maps to NM_000976.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:131388154 C>T maps to NM_001130438.2 I2059I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:137717707 C>T maps to NM_000093.3 A1675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chr9:139565432 G>A maps to NM_201446.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BL-A3JM-01A-12D-A21A-08 chrX:53672364 G>A maps to ENST00000276009 V134V. 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 chr1:89637585 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 chr1:243668580 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 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 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 chr16:16297361 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 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 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 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 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 chr8:113678639 T>A maps to NM_198123.1 P894P. 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 chr1:17395643 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 chr1:43893962 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 chr1:60336746 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 chr1:93649604 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 chr1:151498240 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 chr1:155172608 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 chr1:171621259 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 chr1:183194781 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 chr1:203453265 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 chr1:235357526 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 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 chr10:33200925 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 chr10:73122190 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 chr10:105903396 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 chr10:124358520 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 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 chr11:56757050 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 chr11:61644426 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 chr11:65341110 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 chr11:67172955 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 chr11:102100668 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 chr11:124310897 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 chr11:126139116 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 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 chr12:21680079 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 chr12:48369178 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 chr12:53911119 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 chr12:56868839 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 chr12:78225382 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 chr12:121882021 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 chr12:131498797 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 chr13:41515450 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 chr13:92560197 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 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 chr14:31574847 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 chr14:51204914 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 chr14:76249832 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 chr14:96807894 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 chr14:104026369 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 chr14:105177450 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 chr15:42568596 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 chr15:53908308 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 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 chr16:3273996 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 chr16:4412078 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 chr16:31195650 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 chr16:67662355 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 chr16:81934315 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 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 chr17:4904540 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 chr17:4925874 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 chr17:27945891 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 chr17:35872726 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 chr17:38711548 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 chr17:41477528 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 chr17:66270074 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 chr17:78353430 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 chr18:3508615 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 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 chr19:7591754 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 chr19:8999055 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 chr19:10692041 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 chr19:39008107 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 chr19:44537160 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 chr19:45655521 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 chr19:54746130 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 chr19:55689629 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 chr19:58982926 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 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 chr2:96952860 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 chr2:103119998 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 chr2:170083084 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 chr2:223389718 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 chr2:227663124 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 chr2:240061421 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 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 chr20:36488326 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 chr20:48130896 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 chr21:45518305 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 chr22:24086953 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 chr22:29752416 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 chr22:37770272 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 chr22:46693368 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 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 chr3:33458291 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 chr3:48423543 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 chr3:50391173 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 chr3:53326413 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 chr3:101390112 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 chr3:129282029 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 chr3:160156856 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 chr3:184009971 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 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 chr4:110442740 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 chr4:128938604 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 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 chr5:10403538 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 chr5:71491836 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 chr5:110818484 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 chr5:140763129 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 chr5:172386932 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 chr6:31609348 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 chr6:33660623 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 chr6:43114420 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 chr6:51929768 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 chr6:134210741 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 chr7:99170384 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 chr7:100695123 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 chr7:132754903 G>C maps to ENST00000448878 S56*. 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 chr8:43211962 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 chr8:99440458 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 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.
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 chr9:101825365 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 chr9:116131968 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 chr9:131517772 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 chr9:138395831 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 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: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: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: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: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: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: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 chr1:17413061 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 chr1:27087920 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 chr1:151861805 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 chr1:155319162 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 chr1:173839956 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 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 chr10:81701776 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 chr10:115947865 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 chr11:16812670 G>A maps to ENST00000448080 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20J-01A-11D-A14W-08 chr11:68703930 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 chr11:72945971 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 chr11:93778979 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 chr11:113210176 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 chr11:123893844 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 chr11:134244147 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 chr12:10959333 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 chr12:54448005 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 chr12:112609067 C>T did not map to a codon.
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 chr13:43643081 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 chr13:46656652 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 chr13:60348371 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 chr14:57270956 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 chr14:94929549 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 chr16:21063187 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 chr16:27640095 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 chr16:67514905 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 chr16:87744969 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 chr16:89940209 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 chr17:3195372 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 chr17:16466490 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 chr17:38140721 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 chr17:48745048 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 chr17:68128890 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 chr17:73554289 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 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 chr19:2210631 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 chr19:2213855 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 chr19:4048049 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 chr19:36218435 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 chr19:37211047 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 chr19:39521862 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 chr19:44235748 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 chr19:48892914 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 chr19:49464128 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 chr19:55263167 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 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 chr2:30976030 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 chr2:37283641 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 chr2:88874948 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 chr2:112740455 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 chr2:112740536 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 chr2:145161506 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 chr2:170506886 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 chr2:198498568 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 chr2:203420556 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 chr2:241468764 G>T maps to ENST00000401804 I214I. 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 chr20:32379154 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 chr20:36982713 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 chr20:42164892 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 chr21:32519264 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 chr21:47359996 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 chr22:29835055 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 chr22:31266641 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 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 chr3:42573762 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 chr3:52264888 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 chr3:112546397 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 chr3:121206873 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 chr3:133494391 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 chr3:158384152 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 chr3:183860564 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 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 chr4:86893234 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 chr4:110882117 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 chr4:183664473 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 chr5:5476187 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 chr5:79950602 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 chr5:140167236 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 chr5:140712086 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 chr6:4049305 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 chr6:30457337 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 chr6:41011325 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 chr6:52268301 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 chr6:136977456 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 chr6:151742432 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 chr7:114304339 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 chr7:138863035 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 chr8:21926965 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 chr8:66619458 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 chr8:128750660 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 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 chr9:94809521 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 chr9:115805728 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 chr9:138903718 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 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:47069374 C>T maps to NM_153280.2 P684P. 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 chr1:12820736 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 chr1:16372137 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 chr1:35370069 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 chr1:51929377 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 chr1:68620904 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 chr1:152777744 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 chr1:154130138 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 chr1:155207266 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 chr1:159273847 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 chr1:182823163 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 chr1:221879667 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 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 chr10:127737959 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 chr11:6244845 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 chr11:68370850 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 chr11:128844493 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 chr12:14976351 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 chr12:49444318 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 chr12:51138368 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 chr12:112174761 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 chr12:120942705 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 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 chr14:93944051 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 chr14:100792528 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 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 chr15:75305072 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 chr16:2011250 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 chr16:19020680 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 chr16:85691123 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 chr17:19845218 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 chr17:34071980 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.
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 chr19:51274694 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 chr19:57286538 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 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 chr2:148705640 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 chr2:168108452 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 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 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 chr21:43161780 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 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 chr22:41752422 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 chr22:42606217 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 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 chr3:155212181 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 chr3:168845828 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 chr4:104510982 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 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 chr5:140517288 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 chr6:28228102 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 chr6:30128417 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 chr6:62887181 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 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 chr7:48280472 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 chr8:133941429 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 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 chr9:138379115 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 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-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 chr1:32673402 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 chr1:114201795 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 chr1:227227862 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 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 chr11:17474773 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 chr11:75439096 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 chr11:92087449 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 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 chr12:51890799 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 chr12:71977787 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 chr12:120159202 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 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 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 chr16:3817749 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 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 chr17:80529634 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 chr19:42793046 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 chr19:49967903 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 chr19:55776710 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 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 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 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 chr3:156234065 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 chr4:69692211 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 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 chr5:127484462 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 chr5:176468220 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 chr6:36168657 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 chr6:56401660 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 chr7:116166724 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 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 chr9:100249559 C>T maps to NM_014290.2 L1008L. 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 chr1:45101241 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 chr1:173454532 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 chr1:220162080 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 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 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 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 chr12:56088079 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 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 chr16:89869699 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 chr17:18082088 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 chr17:47284178 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 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 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 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 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 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 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 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 chr9:133499064 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 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-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 chr1:100920980 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 chr1:144619398 G>A maps to NM_001037675.2 V181V. 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 chr1:201060840 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 chr1:227071518 G>A maps to ENST00000391872 A118A. 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 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 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 chr16:72110370 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 chr17:44109506 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 chr18:74091603 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 chr19:19737748 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 chr19:49713573 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 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 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 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 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 chr3:93761857 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 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 chr4:166414358 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 chr5:140209469 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 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 chr7:139636072 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 chrX:153049815 C>T maps to NM_014370.3 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:10186931 C>G maps to NM_001105562.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:26387812 C>T maps to NM_032588.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:27056159 C>T maps to NM_006015.4 Q386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:31437554 G>A maps to ENST00000373741 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:40701822 A>G maps to NM_012421.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:89290037 G>A maps to NM_006256.2 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:151774211 C>T maps to NM_001004432.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:153723690 C>T maps to ENST00000428986 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:159684366 G>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:161697034 A>T did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:197411331 G>T maps to NM_201253.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:198711036 C>T maps to ENST00000271610 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:201437830 C>T maps to NM_012396.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:205632624 C>T maps to NM_033102.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:207242831 C>T maps to NM_006212.2 R351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:214814563 C>T maps to NM_016343.3 I961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr1:247464048 C>T maps to NM_032752.1 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr10:22616525 C>G maps to NM_005180.6 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr10:74879773 A>C did not map to a codon.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr10:135098626 G>A maps to NM_006659.2 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:1491479 G>A maps to NM_001172223.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:4790532 G>A maps to ENST00000380383 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:6816129 G>C maps to NM_003696.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:22647303 G>C maps to NM_022725.3 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:65063046 C>G maps to NM_002689.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr11:71946358 C>G maps to NM_001567.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:27844716 G>A maps to NM_003622.3 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:56531824 C>A maps to NM_001184796.1 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:70970177 G>A maps to NM_001109754.1 F942F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr12:102455052 G>A maps to NM_016053.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr13:48881461 C>T maps to NM_000321.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr13:79219060 A>G maps to NM_024546.3 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr13:103450975 A>C maps to NM_024089.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:23299419 C>T maps to NM_178336.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:68273294 C>G maps to NM_015346.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:69257105 G>C maps to NM_004926.2 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr14:90442141 G>A maps to NM_018319.3 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:33358804 G>C maps to NM_001103184.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:52074979 G>A maps to NM_014548.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:74912355 C>T maps to NM_001130028.1 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr15:74927825 G>C maps to NM_025083.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:15045812 C>G maps to NM_006985.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:28997738 G>A maps to NM_014387.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:30199707 C>A maps to NM_007074.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:56385393 C>G maps to NM_020988.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr16:71701148 G>C maps to NM_015020.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:2605235 C>G maps to NM_015229.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:5365686 C>T maps to ENST00000457531 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:26879508 G>A maps to NM_005148.3 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:30807592 C>T maps to NM_002815.2 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:41907105 G>A maps to ENST00000398393 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:42232691 C>A maps to NM_024032.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:57917166 C>T maps to NM_030938.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:61995218 G>A maps to NM_000515.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:66872822 C>T maps to NM_007168.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:72846000 G>A maps to NM_000835.3 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr17:79864645 G>A maps to NM_001184917.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr18:9396404 C>T maps to NM_020648.5 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:9526414 G>T maps to NM_006631.2 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:10670040 G>A maps to NM_023008.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:16268237 C>T maps to NM_032855.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:21719682 G>A maps to NM_001001415.2 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:23938260 C>G maps to NM_138286.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:31768940 C>T maps to NM_020856.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:36727470 T>G maps to NM_007145.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:37619282 C>T maps to NM_144689.3 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:38610500 G>A maps to NM_015073.1 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:44417604 G>C maps to NM_003425.3 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:44418217 G>C maps to NM_003425.3 S457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:44571039 C>T maps to NM_013361.4 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr19:58371384 C>T maps to NM_032828.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:74043854 C>T maps to NM_001080474.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:103128723 G>C maps to NM_001011552.3 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:152470789 A>G maps to NM_001164507.1 D3867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:169939947 C>T maps to NM_001142271.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:198508943 C>A maps to NM_144629.2 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:207310118 C>T maps to NM_003812.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:220437227 C>T maps to NM_002191.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:231683404 C>T maps to NM_001130850.1 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:237103688 C>T maps to NM_212556.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr2:241706750 G>C maps to ENST00000373308 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr20:37357239 C>G maps to NM_080552.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr21:45817727 G>A maps to ENST00000397932 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr22:24759249 C>A maps to NM_015330.2 S922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr22:46929663 G>C maps to NM_014246.1 S1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:47447451 C>T maps to NM_015466.2 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:121208085 G>C maps to ENST00000393672 S1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:124066027 C>A maps to NM_001024660.3 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:180693956 C>T maps to NM_005087.3 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr3:185191525 C>T maps to NM_004721.3 R803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:6335372 G>A maps to NM_181876.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:38022295 C>T maps to NM_015173.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:39448976 G>C maps to NM_175737.3 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:44680683 C>T maps to NM_021927.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr4:156634389 G>A maps to NM_001130684.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:23521273 C>G maps to NM_020227.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:80369169 C>T maps to NM_006909.1 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:112363127 C>T maps to NM_001085377.1 L977L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr5:149758895 G>A maps to ENST00000451292 Q861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:13182824 C>T maps to NM_030948.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:20126921 G>A maps to NM_001080480.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:26407947 G>T maps to NM_007048.5 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:31079482 C>T maps to NM_014070.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:34802628 C>G maps to NM_017754.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:42146055 C>A maps to NM_000409.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:46977847 G>A maps to ENST00000283297 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr6:64421840 C>T maps to NM_015153.2 Q1453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:2269701 G>A maps to NM_003550.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:47876632 G>A maps to NM_138295.3 Y1943Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:122635436 G>A maps to NM_016945.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr7:129394930 G>A maps to ENST00000393231 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr8:92972520 C>T maps to NM_175634.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr8:144377991 C>A maps to NM_030895.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr9:21202053 G>C maps to NM_021057.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chr9:139741082 C>T maps to NM_001080482.2 I739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chrX:22056608 C>T maps to NM_000444.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20R-01A-12D-A16O-08 chrX:70321315 C>A maps to NM_005938.3 V412V. 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 chr1:65145287 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 chr1:78045313 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 chr1:150443791 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 chr1:247464252 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 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 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 chr11:57958522 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.
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 chr11:71719866 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 chr11:118529681 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 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 chr12:95918478 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 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 chr13:115008756 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 chr14:21556226 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 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 chr16:3820791 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 chr16:4862197 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 chr16:47347637 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 chr16:71805128 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 chr17:62865277 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 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 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 chr19:36728008 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 chr19:44514436 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 chr19:46973830 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 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 chr2:43458381 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 chr2:101580598 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 chr2:198498721 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 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 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 chr22:39708980 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 chr22:43520162 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 chr22:46725394 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 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 chr3:49043564 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 chr3:57827094 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 chr3:124738227 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 chr3:129023616 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 chr3:197408131 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 chr4:26959235 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 chr4:189026056 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 chr5:140476447 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 chr5:140567182 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 chr5:147715196 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 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 chr6:28327554 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 chr6:43194089 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 chr6:150387241 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 chr7:124475364 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 chr7:154561136 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 chr8:33346597 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 chr8:69046487 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 chr8:109228655 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 chr9:95274342 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 chr9:139945963 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 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 chr1:3703762 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 chr1:82451024 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 chr1:245809540 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 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 chr10:63170340 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 chr11:76175123 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 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 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 chr16:89788954 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 chr17:78936368 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 chr20:62657329 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 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 chr3:119451309 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 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 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 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 chrX:73962898 G>C maps to NM_001008537.2 S498*. 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 chr1:161276711 C>A 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 chr11:7642182 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 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 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 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 chr17:40642596 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 chr19:39086327 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 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 chr2:235405158 G>A maps to ENST00000339728 A24A. 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 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 chr5:180057287 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 chr6:163984653 C>T maps to ENST00000361752 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A20W-01A-21D-A14W-08 chr7:129908840 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 chr8:135615034 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 chr9:104314696 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 chrX:115573894 A>G maps to NM_007231.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:1451458 C>G maps to NM_018188.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:4832501 C>T maps to NM_018836.3 C360C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:6189099 C>T maps to NM_015557.2 Q1139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:16265920 G>A maps to NM_015001.2 *3665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:21212780 A>G maps to NM_001198801.1 D759D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:24383901 G>A maps to ENST00000330966 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:36752824 C>T maps to NM_005119.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:39876749 C>T maps to NM_015038.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:45268644 G>A maps to NM_004073.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:55523772 G>A maps to NM_174936.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:55566514 C>T maps to NM_015306.2 W1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:86591601 A>C maps to NM_152890.5 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:89449392 C>T maps to NM_019610.5 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:93646362 C>T maps to NM_206886.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:108742613 C>T maps to NM_013386.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:111989759 C>T maps to NM_024102.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:113638960 T>C maps to NM_014813.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:117629134 C>G maps to NM_003594.3 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:154493837 A>G maps to NM_001098475.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:154962649 T>A maps to NM_025207.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:161696643 G>A maps to NM_001002901.2 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:172357751 A>G maps to ENST00000359070 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:185056734 G>A maps to NM_007212.3 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:196342325 A>G maps to NM_198503.2 C449C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:200014629 C>T maps to NM_205860.1 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:204379891 G>A maps to NM_032833.3 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:208390235 C>T maps to NM_025179.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:216591899 G>A maps to ENST00000366943 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:223986193 C>T maps to NM_001031685.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:229625721 G>A maps to NM_018230.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr1:232551309 C>T maps to NM_020808.3 L1564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:486826 G>A maps to NM_014974.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:13782238 G>A maps to NM_018027.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:27793339 C>T maps to NM_021252.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:70940253 G>A maps to NM_003171.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:123258015 T>C maps to ENST00000351936 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:123845110 G>A maps to NM_206862.2 K1032K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr10:126370703 G>A maps to NM_014661.3 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:703011 C>T maps to ENST00000449452 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:763391 C>T maps to NM_006755.1 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:9161319 G>A maps to NM_015213.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:14666331 C>T maps to NM_000922.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:14913752 G>C did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:27389569 G>A maps to NM_018490.2 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:32410604 C>G maps to NM_024426.4 *518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:57467490 G>A maps to NM_015457.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:58384282 A>G maps to NM_053023.4 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:60184147 G>A maps to NM_032597.3 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:64023081 C>T maps to NM_000932.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:64669496 G>A maps to ENST00000421419 G1354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:67161231 G>A maps to NM_004584.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:73849869 G>A maps to ENST00000334126 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:94554951 C>T maps to NM_130847.2 Q460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr11:130773220 T>C maps to NM_014758.2 E834E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:2795356 A>G maps to NM_199460.2 E1985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:6442924 G>A maps to NM_001065.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:40499283 G>A maps to NM_052885.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:41327359 A>T maps to NM_001843.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:46287314 C>T maps to NM_152641.2 R1754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:48723370 G>A maps to NM_181788.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:52627000 A>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:53186527 A>G maps to ENST00000309505 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:54115351 C>T maps to NM_020898.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:55714719 C>T maps to NM_001005182.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:55846107 A>G maps to NM_054105.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:56396034 C>T maps to NM_001032387.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:63195922 G>A maps to NM_020700.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:79689916 C>G maps to NM_005639.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:82147868 A>G maps to NM_003625.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:91449641 T>C maps to NM_007035.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:104336507 G>A maps to NM_003299.1 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr12:124311274 G>A maps to NM_207437.3 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:20220722 G>A maps to ENST00000414242 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:33327663 A>G maps to ENST00000400481 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:39621937 C>T maps to NM_001012754.2 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:42763215 G>A maps to NM_178009.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:53035695 A>G maps to NM_001098525.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:77669734 G>A maps to NM_015057.4 V3319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:77852998 T>C maps to NM_015057.4 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:98086807 C>T maps to NM_021033.6 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:99083316 G>A maps to NM_005766.2 W642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr13:113893834 G>T maps to NM_001008895.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:30046444 C>T maps to NM_002742.2 *913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:37739686 C>T maps to NM_001195296.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:45414369 C>T maps to ENST00000355081 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:60945039 G>A maps to NM_174978.2 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:70634194 C>T maps to NM_183002.1 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr14:92466416 T>A maps to NM_004239.3 A1531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:24922846 G>A maps to NM_018958.2 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:29561648 C>T maps to NM_138704.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:40241432 G>A maps to NM_001013703.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:69327744 C>T maps to NM_024505.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:74640359 G>A maps to NM_000781.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:81636365 G>A maps to ENST00000454937 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr15:90976973 T>C maps to NM_003870.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:28603635 G>A maps to NM_001054.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:31341892 G>A maps to NM_001145808.1 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:50332876 C>T maps to NM_001114.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:84778353 A>G maps to NM_005153.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr16:88877970 G>A maps to NM_000485.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:6941693 C>T maps to NM_201566.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:7329871 G>T maps to NM_175734.4 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:10628431 A>G maps to NM_001004313.1 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:29679407 C>T maps to NM_001042492.2 Q2531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:33325293 G>A maps to NM_013975.3 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:42427116 C>G maps to NM_002087.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:44954077 G>A maps to NM_003396.1 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:46690569 C>T maps to NM_024016.3 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:47013601 G>A maps to NM_007241.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:47486812 T>C maps to NM_002634.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:48450604 G>A did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:55950042 G>A maps to NM_017949.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:61615787 C>T maps to NM_030779.2 P573P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A2LB-01A-11D-A18F-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:72848654 G>A maps to NM_000835.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:73813468 C>T maps to NM_001080419.1 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:76134244 C>T maps to NM_152468.4 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:79220204 C>T maps to NM_001037984.1 Q837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:79257210 G>A maps to NM_001037984.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr17:80899326 C>T maps to NM_005993.4 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:21084404 C>G maps to NM_013326.3 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:21148962 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:22805189 C>A maps to NM_015461.2 E898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr18:44595907 C>T maps to ENST00000356157 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:2276227 G>A maps to NM_198532.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:7992107 C>T maps to NM_006351.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:41096302 C>T maps to NM_138392.3 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr19:55493758 A>G maps to NM_017852.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:3730542 C>T maps to ENST00000403787 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:16082290 C>T maps to NM_005378.4 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:26703758 C>G maps to NM_194248.2 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:26739467 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:38956809 G>A maps to NM_138801.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:39664038 G>A maps to NM_003618.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:47378468 C>T maps to NM_001163561.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:48848386 C>T maps to NM_172311.2 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:50850595 A>G maps to ENST00000404971 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:66664921 G>A maps to ENST00000407092 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:67630884 G>A maps to NM_019002.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:70315789 C>T maps to NM_006196.3 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:77745830 G>T maps to NM_001134745.1 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:110373334 C>T maps to NM_023016.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:113532666 G>A maps to NM_000575.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:127834282 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:135922245 C>T maps to NM_001172435.1 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:139308577 C>T maps to NM_001001664.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:160257123 G>A maps to NM_013450.2 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:168725896 C>T maps to NM_020981.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:179422795 A>G maps to NM_133378.4 I26527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:206921330 C>T maps to NM_017759.4 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:224849560 C>T maps to NM_001136530.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:231035335 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:231936986 C>T maps to NM_002807.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr2:233651881 T>G maps to ENST00000373566 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:139535 C>T maps to NM_139074.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:6025247 G>C maps to NM_152611.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:20020279 G>A maps to NM_016652.4 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:23375802 A>G maps to ENST00000431864 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:25657488 C>T maps to NM_015655.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:30193213 C>T maps to NM_002165.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:34459578 G>A maps to NM_016436.4 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:44803690 G>A maps to NM_021248.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:46292923 G>C maps to NM_001161841.1 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:50400860 G>C maps to NM_020436.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr20:61588227 G>A maps to NM_022082.3 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:10934120 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:26978899 G>C maps to NM_080794.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:30959909 C>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:34003937 T>C maps to NM_003895.3 Q1402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:37571420 C>T maps to NM_005128.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:45522806 C>T maps to NM_003274.4 F1165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr21:46685468 C>T maps to NM_133635.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:21380551 C>T maps to NM_005446.3 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:21988322 A>T maps to NM_152612.2 K29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:22322013 C>T maps to NM_003935.3 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:38541623 C>T maps to NM_003560.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:41513288 C>T maps to NM_001429.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr22:50609336 C>T maps to NM_052839.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:4818946 G>A did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:10420032 G>A maps to NM_001001331.2 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:12195843 G>A maps to NM_003256.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:50685458 G>A maps to NM_004635.3 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:52812033 G>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:65346991 C>T maps to NM_001033057.1 E1172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:96706688 T>C maps to NM_001080448.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:111785290 C>T maps to ENST00000443106 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:124952080 G>A maps to NM_021964.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:126724991 C>T maps to NM_032242.3 F656F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:130405055 A>G maps to NM_014602.2 I1158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:152880937 G>A maps to NM_002886.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:172365739 G>C maps to NM_001146276.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:179119063 T>C maps to NM_021629.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:180630520 C>T maps to NM_005087.3 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr3:183209962 G>A maps to NM_130446.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:6107460 G>A maps to NM_001099433.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:69962753 C>T maps to NM_001074.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:79430000 C>T maps to NM_025074.6 P3207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:79430150 C>T maps to NM_025074.6 V3257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:90034835 C>T maps to NM_145715.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:100047779 G>A maps to ENST00000505590 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:140299922 G>A maps to NM_057175.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:148605048 C>T maps to NM_138364.2 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:155305518 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr4:167921548 G>A maps to NM_016950.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:54922435 G>A maps to NM_173514.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:94891053 G>A maps to NM_198150.2 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:112154980 G>T maps to NM_001127510.2 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:134074447 G>A maps to NM_001745.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:139938223 G>C maps to ENST00000354402 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:141244800 G>A maps to NM_032420.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:148743623 G>C maps to NM_024028.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:151784386 G>T maps to NM_020167.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:157171171 G>A maps to NM_173491.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:162894720 G>A maps to NM_001142556.1 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:172386962 C>T maps to NM_016093.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:176831014 C>T maps to NM_000505.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr5:180660708 C>T maps to NM_033549.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:13206113 A>G maps to NM_030948.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:32815406 G>A maps to NM_000593.5 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:32908578 G>A maps to NM_002118.4 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:36287384 G>A maps to NM_001010903.4 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:117631383 C>A maps to NM_002944.2 V2098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr6:131216208 G>C maps to NM_001431.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:28996567 G>A maps to NM_014817.3 C365C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:44739759 C>T maps to ENST00000444676 F832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:84649546 A>G did not map to a codon.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:107594020 G>A maps to NM_002291.2 F1011F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:121738841 T>C maps to NM_005763.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:127251628 C>T maps to NM_006193.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:134894411 G>A maps to NM_014149.3 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr7:151945667 T>C maps to ENST00000355193 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:6378703 G>C maps to NM_001147.2 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:41355113 C>T maps to NM_001002296.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:53853102 C>T maps to NM_005285.3 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:57228774 G>A maps to NM_138969.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:61655514 T>C maps to NM_017780.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:66517677 G>A maps to NM_018120.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:69104736 C>T maps to NM_024870.2 I1527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:72977733 A>T maps to NM_007332.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:87241990 G>A maps to NM_138817.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:87442958 G>T maps to NM_007013.3 G456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:101083754 A>G maps to NM_015668.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:113308173 T>C maps to NM_198123.1 G2834G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:124975539 A>C maps to NM_001039112.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:127569331 C>T maps to NM_174911.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:145580112 G>A maps to NM_012162.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr8:145659459 G>A maps to NM_013432.4 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:3828334 G>A maps to NM_001042413.1 F910F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:5304390 G>A maps to NM_134441.1 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:90501166 C>T maps to NM_178828.4 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:97844945 G>A maps to NM_001193329.1 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:100388270 G>T maps to NM_139246.4 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:125391655 C>T maps to NM_001004450.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:130027209 G>A maps to NM_032293.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chr9:140093629 G>A maps to NM_001128228.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:2945384 T>C maps to NM_001011719.1 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:10535149 C>T maps to NM_001193277.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:31947823 G>C maps to ENST00000357033 L2267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:46434112 C>T maps to NM_019886.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:55028738 G>A maps to NM_014481.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:73963125 C>T maps to NM_001008537.2 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:75003929 G>A maps to NM_138703.4 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:99854575 C>T maps to NM_022144.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LB-01A-11D-A18F-08 chrX:117960325 G>A maps to NM_173798.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:6585955 C>T maps to NM_024654.4 E689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:171484972 A>G maps to ENST00000392078 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:210856623 C>T maps to NM_172362.2 *990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr1:212798486 C>T maps to NM_153606.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr11:100211903 A>G maps to NM_014361.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr11:119547810 C>T did not map to a codon.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr12:7970477 G>A maps to NM_153449.2 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr12:94648978 G>A maps to NM_005761.1 E998E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr12:130185154 C>T maps to NM_133448.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr14:36004657 C>A maps to NM_032594.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr15:41247689 T>C maps to NM_024111.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr15:65625613 C>T maps to NM_004884.3 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:30718976 C>T maps to NM_006662.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:30720938 C>T maps to NM_006662.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:66592157 C>T maps to NM_016951.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr16:69385671 C>A did not map to a codon.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr17:38347662 C>T maps to ENST00000456989 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr17:39274426 G>A maps to NM_033059.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr18:32418762 C>T maps to NM_001390.4 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr18:67365703 G>A maps to NM_152721.5 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr2:219514051 G>A maps to NM_001105537.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr21:22696784 C>A maps to NM_004540.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr3:46415256 G>A maps to NM_001100168.1 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr3:101212806 T>C maps to NM_020654.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr4:6473932 C>T maps to NM_020416.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr4:125591959 T>C maps to NM_020337.2 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr5:74069826 C>T maps to NM_014886.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr5:133914400 C>T maps to ENST00000448712 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr6:32154670 G>A maps to NM_002586.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr6:111688579 T>C maps to NM_002912.3 K2137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:15652117 G>C maps to NM_005924.4 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:30704744 G>A maps to ENST00000348438 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:66459243 G>A maps to NM_016038.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr7:94917927 T>C maps to NM_001166160.1 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr8:42260957 G>A maps to ENST00000417062 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr8:104394803 C>T maps to NM_138455.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr9:104124823 C>T maps to NM_001701.3 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chr9:116840417 C>T maps to NM_001633.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A2LD-01A-12D-A20D-08 chrX:15605981 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:1572547 C>G maps to ENST00000401097 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:1635766 C>G maps to NM_024011.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:10342590 G>A maps to ENST00000377086 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:11708843 G>A maps to NM_012168.4 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:12337496 C>G maps to NM_015378.2 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:22141308 C>T maps to NM_001013693.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:27106491 G>T maps to NM_006015.4 E2035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:27189726 G>A maps to NM_006142.3 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:31347174 C>T maps to NM_014654.3 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:33363912 C>G maps to NM_033504.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:35485179 G>A maps to NM_007167.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:46751934 G>C maps to ENST00000254454 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:60297858 C>T maps to NM_015888.4 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:87379770 C>G maps to NM_004261.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:90179370 G>A maps to NM_032270.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:110592107 G>A maps to NM_033088.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:143912362 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:145075663 C>A maps to NM_022359.5 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:150532596 C>T maps to ENST00000369039 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:151316208 G>A maps to NM_000449.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:156100506 C>G maps to NM_170707.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:157665208 G>A maps to NM_052939.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:159169586 C>T maps to NM_021189.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:160262954 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:160681498 G>A maps to NM_001778.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:167408586 G>C maps to NM_198053.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:168056840 C>A maps to NM_153832.1 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:183920229 G>C maps to NM_015101.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:203467965 G>C maps to NM_014359.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr1:206649606 G>T maps to NM_014002.3 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:50819247 G>A maps to NM_003055.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:91066853 C>T maps to NM_001547.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:115607067 G>A maps to NM_014881.3 Q718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr10:127824154 G>A maps to NM_003474.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:5142103 C>T maps to NM_001005222.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:33763507 C>G maps to NM_012175.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:62414896 G>A maps to NM_030628.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:65961018 C>G maps to NM_018026.2 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr11:134183856 C>T maps to NM_001080407.2 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:10999682 G>A maps to NM_007244.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:50029642 C>T maps to NM_001031698.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:53412670 C>A maps to ENST00000438209 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:56996517 C>A maps to NM_013449.3 E1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:96354208 C>T maps to NM_152435.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:112530904 G>A maps to NM_024953.3 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:124398989 C>T maps to NM_207437.3 D3371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr12:130926566 C>A maps to NM_015347.4 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr13:37269506 C>T maps to NM_203451.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr13:77642918 G>C maps to NM_015057.4 V3984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:20876253 G>A maps to NM_007110.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:64522741 C>T maps to NM_182914.2 L3275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr14:72176164 C>G maps to NM_015556.1 S1352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr15:63008573 G>C maps to NM_015059.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr15:75641327 G>T maps to NM_024608.2 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr15:99467846 C>T maps to NM_000875.3 Q906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:1412125 G>A maps to NM_032520.4 Q135Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A3PH-01A-11D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:2580758 G>A maps to NM_001048212.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:4556894 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:21136610 G>C maps to NM_017539.1 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:21172531 C>G maps to ENST00000451578 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:28948443 C>T maps to NM_001178098.1 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:30777494 G>A maps to NM_014771.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:56857668 G>A maps to NM_014669.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:56899425 C>G maps to NM_000339.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:67195735 C>T maps to NM_018378.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:67575860 C>G maps to NM_001193523.1 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:68721628 C>T maps to NM_001793.4 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:88677719 C>G maps to ENST00000452588 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr16:88870298 C>T maps to NM_030928.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:1378123 G>T maps to NM_001080779.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:29554249 C>T maps to NM_001042492.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:36485623 C>T maps to ENST00000398597 S1277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:36486595 C>T maps to ENST00000398597 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:36487081 C>T maps to ENST00000398597 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:39279804 G>A maps to NM_031854.2 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:73949632 G>C maps to NM_004035.6 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr17:74900407 C>T maps to NM_198955.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr18:6961982 G>C maps to NM_005559.2 L2471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr18:21120456 C>G maps to NM_000271.4 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:5745939 C>G maps to NM_152784.3 S225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:8386221 G>A maps to NM_005001.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:11034008 G>A maps to NM_024029.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:17953846 C>T maps to NM_000215.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:18968268 G>C maps to ENST00000418384 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:47181773 C>T maps to ENST00000449438 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:49000752 G>A maps to NM_001080434.1 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:49965029 G>A maps to NM_153329.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:52618745 G>A maps to NM_178523.3 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:55645271 G>A maps to NM_003283.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:56466731 C>T maps to NM_176811.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:56895394 G>C maps to NM_144690.1 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr19:59073564 C>T maps to NM_198055.1 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:11802147 C>T maps to NM_012344.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:26624902 G>T maps to NM_145038.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:27360540 C>T maps to NM_178553.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:27600418 G>T maps to NM_144631.4 S540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:40656480 C>A maps to NM_021097.2 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:61175206 G>A maps to NM_144709.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:74689844 C>T maps to NM_006302.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:74907020 C>T maps to NM_004263.3 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:86707393 C>T maps to NM_001146688.1 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:98206121 G>A maps to NM_025190.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:116485504 A>G maps to NM_020868.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:125555700 G>A maps to NM_130773.2 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:130911410 G>C maps to NM_017951.4 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr2:135655918 C>T maps to NM_138326.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:30956841 C>G maps to ENST00000375687 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:33703304 G>A maps to NM_018217.2 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:35243656 G>C maps to NM_032214.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:44571880 C>T maps to NM_022104.3 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr20:62659060 C>T maps to NM_012469.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:19459218 G>C maps to ENST00000399525 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:24179996 G>A maps to NM_001135751.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:42609616 C>T maps to NM_005650.1 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:50682165 G>C maps to NM_020461.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr22:50682725 G>A maps to NM_020461.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:52561906 C>G maps to NM_001134231.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:107798973 G>A maps to NM_001777.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:118906731 G>A maps to NM_006952.3 W60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:121822488 G>C maps to NM_175862.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:123019118 G>A maps to NM_183357.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:130287161 G>C maps to NM_001102608.1 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr3:160253310 G>A maps to NM_002268.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:517588 G>A maps to NM_001127178.1 W652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:3208580 C>G maps to NM_002111.6 L1982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:9987350 G>A maps to NM_020041.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:71634326 G>C maps to NM_001037442.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:91230190 C>G maps to NM_001145065.1 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:95583675 C>T maps to NM_006457.3 C563C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:108824403 C>T maps to NM_152621.5 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr4:169204636 G>C maps to NM_017631.5 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:16668555 G>A maps to NM_012334.2 Q1969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:38884064 G>A maps to NM_003999.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:80422971 G>C maps to NM_006909.1 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:118965402 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:140202694 C>A maps to NM_018908.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:150934192 G>A maps to NM_001447.2 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:154267889 G>T maps to NM_015465.3 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:172660108 C>T maps to NM_004387.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr5:179143167 C>T maps to ENST00000415618 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:12123623 C>G maps to NM_002114.2 S1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:12123633 C>T maps to NM_002114.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:30514512 G>A maps to NM_005275.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:32046816 G>A maps to ENST00000375244 G1456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:32977304 G>C maps to NM_002119.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:34985274 G>C maps to NM_015245.2 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:36020526 C>T maps to NM_139012.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:36823786 G>A maps to NM_016059.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:40399706 G>C maps to NM_020737.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:150210658 G>C maps to NM_139165.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr6:157256699 C>G maps to ENST00000367148 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:18767219 G>A maps to NM_178425.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:45115442 G>A maps to NM_001029835.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:73790515 G>A maps to NM_003388.4 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:92838028 G>A maps to ENST00000453812 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:98634776 G>A maps to NM_020429.2 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:105111174 G>C maps to NM_019042.3 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:148288195 T>A maps to NM_145304.2 L60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr7:149419540 G>A maps to NM_032534.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:73848264 A>G maps to NM_004770.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:103323974 G>A maps to NM_015902.4 F802F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:120977540 C>T maps to NM_022783.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:134239871 C>T maps to NM_003882.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:142229061 C>T maps to NM_001080431.1 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr8:144946755 G>A maps to NM_031308.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:3257089 C>T maps to NM_134428.1 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:14824957 G>A maps to ENST00000380880 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:80912184 C>G maps to ENST00000421149 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:107289385 G>A maps to NM_001001919.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:123550365 G>C maps to NM_012164.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:127691528 C>T maps to NM_002077.3 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:131767775 C>T maps to NM_015354.1 F1568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:139303519 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:140115103 G>C maps to NM_031297.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chr9:140115580 G>T maps to NM_031297.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chrX:37664366 C>T maps to NM_000397.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chrX:44941857 C>G maps to NM_021140.2 S1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PH-01A-11D-A21Z-08 chrX:71350505 G>T maps to NM_001024455.3 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:8390857 G>A maps to ENST00000377479 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:8399580 C>T maps to ENST00000377479 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:11708768 G>A maps to NM_012168.4 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:17552409 G>A maps to NM_013358.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:27057834 C>T maps to NM_006015.4 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:36301441 G>A maps to NM_017629.2 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:64643838 G>A maps to NM_005012.2 V705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:92433809 C>A maps to ENST00000347608 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:109793957 C>G maps to NM_001408.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:109795715 C>T maps to NM_001408.2 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:145109580 G>A maps to NM_004892.4 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:156105708 G>A maps to NM_170707.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:156594200 G>A maps to NM_021817.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:160328024 C>T maps to NM_015331.2 F698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:162337158 G>T maps to NM_014697.2 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:182368981 C>T maps to NM_172000.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:201030502 G>A maps to NM_000069.2 I1049I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:224477269 C>T maps to NM_002533.2 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr1:227071518 G>A maps to ENST00000391872 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:28897266 C>T maps to NM_016628.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:45430143 G>C maps to NM_001123376.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:55826640 G>C maps to NM_001142763.1 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:63852164 G>C maps to NM_032199.2 V981V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:72300934 C>A maps to NM_014431.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:113928631 G>C maps to NM_020918.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:113928679 G>A maps to NM_020918.4 F275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:116734975 A>T maps to NM_139169.4 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr10:123844549 C>G maps to NM_206862.2 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:2432684 C>G maps to ENST00000452833 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:8947367 G>C maps to NM_020643.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:14665989 C>T maps to NM_000922.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:19256465 C>T maps to NM_024680.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:60070048 A>G maps to NM_148975.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:61570833 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:61580783 C>T maps to NM_013402.4 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:62376049 G>A maps to ENST00000278845 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:64030226 C>T maps to NM_000932.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:64972253 C>G maps to NM_005186.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:65363054 C>A maps to NM_033347.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:71949114 C>T maps to NM_001567.3 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:73066681 C>G maps to NM_014786.3 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:94134383 G>T maps to NM_016540.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:94759440 G>C maps to NM_001161630.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:117089802 G>C maps to NM_004716.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:119181613 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:119182860 C>T maps to NM_006500.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr11:119183624 C>G maps to NM_006500.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:284198 G>C maps to NM_001170738.1 *1183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:7175802 G>A maps to NM_001734.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:31632936 C>A maps to NM_144973.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:49494207 G>A maps to NM_018113.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:50616214 C>T maps to NM_001113546.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:51207890 C>T maps to NM_005171.4 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:54920518 C>T maps to NM_005337.4 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:56749505 G>A maps to NM_005419.3 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:57638145 T>A maps to NM_145064.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:119583319 C>T maps to NM_194286.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:121615183 C>T maps to NM_002562.5 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr12:133384935 G>C maps to NM_005895.3 S240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:37394042 G>A maps to NM_000538.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:39621832 T>C maps to NM_001012754.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:102029157 C>T maps to NM_052867.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr13:103279420 C>A maps to ENST00000376052 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:23588120 C>T maps to NM_001805.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:31535512 G>A maps to NM_007077.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:55852661 C>A maps to NM_014924.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:68086726 C>T maps to NM_001172.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr14:74179619 C>T maps to NM_006029.4 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:33916208 C>T maps to NM_001036.3 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:40512773 T>C maps to ENST00000412359 D1003D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:42202031 C>T maps to NM_139265.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:54003546 A>G maps to NM_182758.2 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:63948073 G>A maps to ENST00000261887 L3317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:64010868 T>C maps to ENST00000261887 S1294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:64067651 G>C maps to ENST00000261887 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:64455080 C>T maps to NM_000942.4 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:65871970 A>C maps to ENST00000420799 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:69561006 G>C maps to NM_015554.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:80767364 C>G maps to NM_014862.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr15:85407672 G>A maps to NM_020778.4 E1702E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:67314064 C>T maps to NM_001129729.1 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:67877393 G>T maps to NM_020457.2 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:70531254 C>T maps to NM_015386.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr16:76592576 C>T maps to NM_033401.3 F1307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:9153948 C>T maps to NM_004853.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:15942888 G>A maps to ENST00000395857 L2286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:18565288 G>A maps to NM_001145045.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:27010764 C>T maps to NM_003170.3 F720F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:27051728 G>C maps to NM_138463.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:33259397 G>C maps to NM_006584.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:33482389 C>T maps to NM_173167.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:38445696 C>T maps to NM_001254.3 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:38910243 G>A maps to NM_181534.3 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:40716812 G>A maps to NM_001042532.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:43195689 G>A maps to NM_133373.3 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:46628331 C>T maps to NM_002146.4 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:48614132 G>A maps to NM_017957.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:53844766 C>T maps to NM_021213.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:62523290 T>C maps to NM_138363.1 T405T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A3PJ-01A-21D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:72353374 C>T maps to ENST00000440684 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:73316529 G>C maps to NM_002086.4 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:76503683 G>A maps to ENST00000389840 S1476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr17:78073332 C>G maps to NM_017950.2 S1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr18:3499317 C>T maps to NM_004746.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:3290310 C>T maps to NM_021938.3 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:5719792 G>A maps to NM_004793.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:7734743 G>A maps to NM_020415.3 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:10897349 C>T maps to NM_001005361.2 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:11287303 G>A maps to NM_015493.6 H578H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:15355562 C>T maps to NM_058243.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:31040308 G>A maps to NM_014717.1 P1261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:35940870 G>A maps to NM_005306.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:36393521 C>T maps to NM_014266.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:42558024 G>A maps to NM_002088.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:47933516 G>A maps to NM_015063.2 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:48229177 C>T maps to NM_014601.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:49238512 G>A maps to NM_017805.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:49658060 G>C maps to NM_002152.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:51499315 C>T maps to NM_144505.1 *306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr19:55087421 G>T maps to NM_001130917.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:24538093 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:32832644 C>T maps to NM_016252.3 R4732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:33813493 G>A maps to ENST00000395190 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:54848570 A>T maps to NM_003128.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:79385577 C>T maps to NM_138937.2 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:86305368 C>T maps to NM_015425.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:108608586 C>T maps to NM_021815.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:109398639 A>G maps to NM_006267.4 K2939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:116066831 C>T maps to NM_020868.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:130878028 G>C maps to NM_001099771.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:131098586 A>C maps to NM_032357.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:131810475 T>C maps to NM_001009993.2 *196W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:175263090 C>G maps to NM_024583.4 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:209108166 G>A maps to NM_005896.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:211513261 G>A maps to NM_001122633.1 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:225751217 T>A maps to NM_014689.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:228157989 A>T maps to NM_000091.4 G1098G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr2:239353165 C>T maps to NM_001040445.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:25297682 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:30584821 C>T maps to NM_001011718.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:30897793 C>T maps to NM_004798.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:44453013 C>T maps to NM_003279.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr20:52199146 G>A maps to NM_006526.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:39671487 C>G maps to NM_170736.1 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:42840424 G>A maps to NM_001135099.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:47746352 G>A maps to NM_006031.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr21:47858171 G>A maps to NM_006031.5 E3065E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr22:40711470 A>T maps to ENST00000454349 S1635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:10138050 C>G maps to NM_033084.3 L1360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:14941940 C>G maps to NM_152536.3 A1062A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:21466995 C>G maps to NM_024697.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:51458410 G>A maps to ENST00000273612 F671F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:64084987 C>T maps to NM_198859.3 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:66449392 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:97618082 C>T maps to ENST00000182096 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:111794168 C>G maps to ENST00000443106 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:132211336 C>T maps to NM_015268.3 Q1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:140675470 G>A maps to NM_001104647.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:160474177 C>T maps to NM_139245.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:167277881 A>G maps to NM_178824.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:170198741 G>A maps to NM_020949.2 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:183432929 A>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr3:194790761 G>A maps to NM_152531.4 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:875738 G>A maps to NM_005255.2 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:1377692 C>T maps to NM_020894.2 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:2935297 G>A maps to NM_001146069.1 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:83740265 G>C maps to ENST00000505472 L1239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:109790267 G>A maps to ENST00000333642 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:153831238 G>T maps to NM_001025595.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr4:154506048 C>T maps to NM_001131007.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:195401 T>G maps to NM_001080478.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:5464729 C>T maps to NM_015325.1 A1761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:33459810 G>A maps to ENST00000455217 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:45353207 C>G maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:78915519 C>T maps to NM_173797.3 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:79279589 G>A maps to ENST00000512528 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:127622541 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr5:141033812 G>A maps to NM_022481.5 Q1447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:1612340 G>A maps to NM_001453.2 *554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:10697684 G>A maps to NM_017906.2 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:33400505 G>A maps to NM_006772.2 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:35478695 C>G maps to NM_003322.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:36887409 C>T maps to NM_152734.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:39846246 G>A maps to ENST00000398904 K476K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:41057403 C>T maps to NM_002505.4 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:46766859 G>A maps to NM_005588.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:52344528 C>T maps to NM_018100.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:53883759 C>G did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:99823965 G>A maps to NM_017421.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:137018500 G>C maps to NM_005923.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr6:152640036 C>T maps to NM_182961.2 A5450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:2311493 G>A maps to NM_013321.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:31682388 C>T maps to NM_194300.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:107746972 A>C maps to NM_007356.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr7:143079494 G>A maps to NM_001010972.1 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:27737164 C>T maps to NM_173833.5 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:71510490 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:95547203 C>T maps to NM_015496.3 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr8:117864826 C>A maps to NM_006265.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:35059693 G>A maps to NM_007126.3 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:71395442 C>T maps to NM_138333.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:91150577 C>T maps to NM_001161625.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:96212867 C>A maps to NM_198841.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:112225591 C>T maps to NM_002829.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:117568271 C>T maps to NM_005118.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:134026094 G>A maps to ENST00000451030 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chr9:138376898 C>T maps to NM_014811.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chrX:37312441 A>T maps to NM_000950.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chrX:99661762 G>A maps to NM_001184880.1 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chrX:112033994 G>A maps to NM_001113490.1 Q648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PJ-01A-21D-A21Z-08 chrX:150911820 C>T maps to NM_005140.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:1337498 A>G maps to NM_017971.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:12405436 C>T maps to NM_015378.2 T2964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:17395637 G>A maps to NM_007365.2 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:22816494 C>T maps to NM_014870.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:23233201 G>C did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:26189907 C>T maps to NM_178422.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:39801742 A>G maps to ENST00000289893 Q1601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:55457706 T>C maps to NM_182532.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:152060607 G>C maps to NM_001008536.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:154141836 C>T maps to ENST00000328159 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:156230277 A>G maps to NM_015327.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:171310692 A>G maps to NM_002022.1 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr1:207300064 C>T maps to NM_000715.3 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:27703134 C>T maps to NM_001034842.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:45430458 C>T maps to NM_001123376.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:64573653 G>C maps to NM_001136178.1 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:64575747 G>A maps to NM_001136178.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr10:65369971 T>G maps to NM_001001330.2 L148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:12901331 T>A maps to NM_021961.5 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:55872741 C>G maps to NM_001005200.1 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr11:103270432 C>T maps to NM_001080463.1 R4074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:431653 C>T maps to NM_001042603.1 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:49433003 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:51318850 G>C maps to NM_014033.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:51865154 T>C maps to NM_001039960.1 D581D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:85459087 C>T maps to NM_001079910.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:96370218 G>A maps to NM_002108.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:99076994 C>T maps to NM_181861.1 F707F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr12:123087590 G>A maps to NM_014708.4 L1634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr13:39446911 C>T maps to NM_207361.4 R2673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr13:76397777 A>G maps to ENST00000357063 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr13:100425083 G>A maps to NM_206808.2 A23A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A3PK-01A-21D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:21870181 C>T maps to NM_001170629.1 Q1332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:55529992 C>T maps to NM_144578.3 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:68040538 C>T maps to NM_020715.2 Q621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:81743986 T>C maps to NM_033104.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:102904528 A>G maps to NM_014844.3 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr14:103390132 C>A maps to NM_030943.3 C43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:35275415 G>A maps to NM_014106.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:40917630 C>T maps to NM_170589.3 I1749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:42171660 G>C maps to ENST00000320955 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:51514602 G>A maps to NM_031226.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:62167120 T>C maps to NM_020821.2 A3456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:66172007 G>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:82575105 T>C maps to NM_001008226.1 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:84651604 G>A maps to NM_207517.2 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:88679229 C>G maps to NM_001012338.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr15:91169175 G>A maps to NM_022769.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:20975224 A>G maps to NM_017539.1 N3327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:28919982 G>A maps to NM_024816.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:30365607 C>T maps to NM_006110.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:55360336 C>G maps to NM_024335.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr16:67576932 G>T maps to NM_001193523.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:2221249 A>C maps to NM_021947.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:15952253 G>C maps to ENST00000395857 Y2162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:19284404 C>A maps to NM_139034.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr17:38346911 C>T maps to ENST00000456989 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:3187532 C>A maps to NM_003803.3 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:7044768 G>A maps to NM_005559.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:19321720 C>T maps to NM_020774.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:28581658 C>G maps to NM_001941.3 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:29049226 T>G maps to NM_001944.2 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:55319835 G>C maps to NM_005603.4 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr18:77664068 G>A maps to NM_025078.4 D241D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:1881472 C>T maps to NM_031213.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:38896258 G>A maps to NM_174905.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr19:49657933 C>G maps to NM_002152.2 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:25180825 G>A maps to NM_016544.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:95847682 T>C maps to ENST00000453539 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:113590326 G>C maps to NM_000576.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:152536297 A>G maps to NM_001164507.1 Y1064Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:177161615 A>G maps to NM_006554.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:219746933 C>T maps to NM_025216.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:228172495 G>A maps to NM_000091.4 W1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr2:233321092 G>A maps to NM_001631.3 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:2463827 G>A maps to NM_024325.4 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:31624293 G>C maps to NM_174897.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:34457363 G>T maps to NM_016436.4 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr20:60904246 C>T maps to NM_005560.3 L1394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr22:23438385 T>C maps to NM_002073.2 Y168Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr22:43459893 C>T maps to NM_012263.4 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:44612225 C>T maps to NM_018651.2 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:47458630 G>A maps to NM_012235.2 L1013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:48687964 G>T maps to NM_001407.2 P2140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:52473770 G>C maps to NM_020163.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:53217514 T>C maps to NM_212539.1 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:108355536 T>G maps to NM_014648.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:119720940 T>C maps to NM_002093.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:125166628 C>T maps to NM_003794.2 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:137843159 C>T maps to NM_016161.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:142226808 C>T maps to NM_001184.3 K1665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr3:184299391 G>A maps to NM_004443.3 T993T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:1807558 C>T maps to NM_000142.4 D576D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:47427923 C>G maps to NM_000812.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:72622631 C>T did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:89352339 T>A maps to NM_017912.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:123122252 C>T maps to NM_015312.3 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr4:123317467 A>G maps to NM_139243.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:482239 C>T maps to NM_004174.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:66440573 C>A maps to NM_001164664.1 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:79855445 T>C maps to NM_001004441.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:132083139 A>G did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:132552956 G>T maps to NM_015082.1 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:139917004 A>G maps to ENST00000253810 P2370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:140764039 T>A maps to NM_018920.2 L525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:177573137 C>T maps to NM_022762.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr5:177640079 C>G maps to NM_153373.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr6:30680686 G>A maps to NM_014641.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr6:158516771 A>G maps to NM_003898.3 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:48015278 A>G maps to NM_004507.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:55214317 G>A maps to NM_005228.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:75615696 C>A maps to NM_000941.2 Y647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:90894815 C>T maps to NM_003505.1 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:99771456 C>A did not map to a codon.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr7:101882762 G>T maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:79960013 C>G maps to ENST00000376646 L2415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:98691011 G>A maps to NM_001010895.2 V550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:112151538 A>G maps to NM_002829.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:112189305 G>A maps to NM_002829.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chr9:136337169 G>A maps to NM_017585.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chrX:102632753 G>T maps to NM_206915.1 *112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A3PK-01A-21D-A21Z-08 chrX:147743711 C>G maps to NM_002025.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:62740331 G>A maps to NM_181712.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:159898435 G>A maps to NM_001135050.1 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:226044657 G>A maps to NM_014698.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr1:245582981 G>T maps to NM_018012.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr10:49658320 G>C maps to ENST00000417912 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr11:4976490 G>T maps to NM_001004748.1 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr13:53313189 G>A maps to NM_007015.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr13:114202740 C>T maps to NM_017905.4 R632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr14:19563460 T>A maps to NM_001005356.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr14:21829275 T>C maps to NM_007192.3 K630K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr14:23828663 T>G maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BT-A42B-01A-32D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:2304012 C>T maps to ENST00000454671 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:11001757 G>A maps to NM_000246.3 A803A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:24902199 G>A maps to NM_052944.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr16:31425841 C>T maps to ENST00000444228 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:13409699 C>T maps to NM_023035.2 W920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:16860862 G>A maps to ENST00000438489 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:19745887 G>A maps to NM_016573.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:50939407 C>T maps to NM_004533.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr19:56200275 G>A maps to NM_001130071.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr20:62200823 G>A maps to NM_001037335.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr20:62338383 G>A maps to NM_003224.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr3:170099113 C>G maps to NM_005414.3 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr4:187539563 G>A maps to ENST00000260147 R2729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr8:52321369 T>C maps to NM_144651.4 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chr8:124382175 A>G maps to NM_014109.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chrX:70471084 C>A maps to ENST00000373988 E243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chrX:77112889 C>T maps to NM_032121.5 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42B-01A-32D-A23M-08 chrX:110439846 C>T maps to NM_001128168.1 Y498Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:7723701 G>A maps to NM_015215.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:11017750 C>T maps to NM_001170754.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:23763090 G>A maps to NM_017707.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:35365868 C>T maps to NM_001080418.1 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:145534180 T>C maps to NM_003637.3 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:150915382 G>A maps to NM_001145415.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:155018906 C>T maps to NM_152494.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:155912333 C>T maps to NM_181885.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:161954645 A>G maps to ENST00000451379 Y534Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:186114896 G>A maps to NM_031935.2 W4817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:197073064 C>T maps to NM_018136.4 L1772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:206782759 A>C maps to NM_006893.2 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:212617720 G>A maps to NM_013349.4 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr1:235884049 G>A maps to NM_000081.2 F3157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:95169 C>T maps to NM_177987.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:23250839 G>T maps to NM_173081.3 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:90672880 C>G maps to NM_020799.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr10:93726463 C>T maps to NM_003972.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:1651189 C>T maps to NM_001001480.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:31824257 A>T maps to NM_001604.4 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:57243960 C>G maps to NM_178570.1 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:62557491 C>T maps to NM_199337.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:66189920 G>A did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:66359148 T>A maps to NM_018219.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr11:123483471 C>G maps to ENST00000456860 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:56480393 G>C maps to NM_001982.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:57985170 C>T maps to NM_024779.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:123078908 A>C maps to NM_014708.4 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr12:124144457 C>A maps to NM_001516.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr13:25276098 C>A maps to NM_001185085.1 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr13:32936816 C>T maps to NM_000059.3 Q2655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr14:20215774 T>C maps to NM_172194.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr14:51288735 G>C maps to NM_020921.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:44951439 G>A maps to NM_025137.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:64017587 A>C maps to ENST00000261887 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:82443992 G>A maps to NM_024580.5 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr15:84581958 G>T maps to NM_207517.2 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr16:10566011 G>A maps to NM_024997.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr16:21133385 G>A maps to NM_017539.1 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr16:31195260 C>A maps to NM_004960.3 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:1680703 C>G maps to NM_002615.4 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:7222371 G>C maps to NM_032442.2 L1227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:39977231 C>T maps to NM_021939.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:41960381 G>C maps to NM_005374.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:61607728 G>A maps to NM_030779.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:74936491 C>T maps to NM_198955.1 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:78162186 G>C maps to NM_024110.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr17:78195376 G>C maps to NM_173626.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr18:2891873 G>A maps to NM_032048.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:1482189 G>T maps to NM_017573.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:1827791 G>A maps to NM_020695.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:2852509 A>G maps to NM_152791.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:15512113 G>C maps to NM_014371.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:18174752 C>T maps to NM_005535.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:38709683 G>A maps to NM_001135155.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:46216532 G>C maps to NM_001080469.1 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:47440613 A>T maps to NM_004491.4 K1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:50266515 C>T did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:55824328 G>A maps to NM_001085488.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr19:58198131 G>A maps to ENST00000356715 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:15448381 T>A maps to NM_015909.2 R1585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:32340841 G>A maps to NM_014946.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:51254844 G>A maps to ENST00000404971 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:55407748 G>T maps to NM_152385.2 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:69002356 G>T maps to NM_001007231.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:105859328 G>A maps to NM_007227.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:111399042 T>C did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:113089650 G>A maps to NM_198581.2 R1052R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:120385259 G>C maps to NM_001029996.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:121747002 G>C maps to NM_005270.4 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:141130655 A>C maps to NM_018557.2 G3563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:159035485 A>G maps to NM_138803.3 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr2:172945091 G>A maps to NM_199227.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:3305599 C>A maps to NM_001009984.1 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:33719492 T>A maps to NM_018217.2 K266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:44181844 G>A maps to NM_130896.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:45354634 C>A maps to NM_030777.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr20:60882814 C>T maps to NM_175573.1 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr21:30255350 T>C maps to NM_013240.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:44490076 C>T maps to NM_181489.5 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:52398862 C>G maps to ENST00000273600 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:71050167 G>T maps to NM_032682.4 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:124436141 G>A maps to NM_001024660.3 L2775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:126208203 C>T maps to NM_001165974.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:155208657 C>G did not map to a codon.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:183670873 C>T maps to NM_005688.2 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr3:186015940 G>A maps to NM_001346.2 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:25677815 G>A maps to NM_006424.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:41984467 C>G maps to NM_001029955.3 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:47033933 C>T maps to NM_000812.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:83557960 G>A maps to NM_001037582.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:88097922 T>G maps to NM_020803.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:123855675 A>G maps to NM_145207.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr4:141489010 G>A maps to NM_021833.4 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr5:71015206 G>A maps to NM_004291.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr5:78671999 T>C maps to NM_004272.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:25921505 A>T maps to NM_005835.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:27425077 T>A maps to NM_007149.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:30035193 G>T maps to NM_021959.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:31110755 G>C maps to NM_001105564.1 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:31733740 C>G maps to NM_025258.2 V806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:33289242 C>T maps to NM_001350.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:116757644 C>T maps to NM_013352.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr6:144508444 C>G maps to NM_003764.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:2978459 C>T maps to NM_032415.4 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:42005112 C>A maps to NM_000168.5 P1186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:44737335 G>C maps to ENST00000444676 R786R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:100469280 C>T maps to NM_003302.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:138764693 T>C maps to ENST00000464606 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr7:142880648 C>A maps to NM_176881.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr8:12958063 G>A maps to NM_182643.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr8:110489536 C>T maps to ENST00000426474 Q3001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:15187021 C>T maps to NM_152574.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:22451127 C>T maps to NM_022160.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:111970251 A>G maps to NM_019114.3 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:131356498 G>A maps to NM_001130438.2 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:131356541 G>T maps to NM_001130438.2 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chr9:131397155 G>A maps to NM_052844.3 F342F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BT-A42C-01A-11D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chrX:2670372 C>A maps to NM_001141919.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BT-A42C-01A-11D-A23M-08 chrX:48762195 G>A maps to ENST00000452555 L358L. 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 chr1:36859514 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 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 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 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 chr16:53967949 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 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 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 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 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 chr22:32647855 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 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 chr3:100364942 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 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 chr5:71494956 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 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 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: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 chr1:32043027 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 chr1:101194672 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 chr1:201056979 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 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 chr11:118376453 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 chr11:125891383 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 chr12:49424158 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 chr12:119942995 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 chr13:35619478 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 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 chr14:105397200 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 chr15:58861006 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 chr16:2155924 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 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 chr17:7701999 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 chr17:51901323 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 chr17:76167699 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 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 chr19:47349396 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 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 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 chr20:34242689 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 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 chr22:38327930 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 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 chr4:55961104 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 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 chr6:167755004 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 chr7:21945944 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 chr7:124404703 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 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 chr8:146033635 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 chr9:35752110 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 chr9:123620305 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 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: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-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 chr1:100459151 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 chr1:197390533 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 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 chr11:9608063 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 chr11:66619973 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 chr11:71698133 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 chr11:103908029 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 chr12:49416551 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 chr12:58021629 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 chr12:70932749 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 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 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 chr15:68504195 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 chr15:91421500 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 chr16:24988547 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 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 chr17:40936119 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 chr17:66933152 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 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 chr19:2216318 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 chr19:49971799 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 chr19:54656168 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 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 chr2:54159083 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 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 chr21:43767667 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 chr22:46792542 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 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 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 chr4:24801247 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 chr4:57250455 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 chr4:104103930 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 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 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 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 chr9:100888881 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 chr9:132658258 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 chr9:139391497 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 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: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: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.
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 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 chr11:94231643 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 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 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 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 chr19:11486190 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 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 chr2:196865505 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 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 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 chr3:195511814 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 chr4:100479210 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 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 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 chr7:100187840 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 chr8:77776410 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 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 chr1:16111107 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 chr1:45115331 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 chr1:52705107 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 chr1:152285756 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 chr1:186319406 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 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 chr10:50857601 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 chr10:74619016 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 chr10:129905873 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 chr11:12248644 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 chr11:28232682 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 chr11:123900607 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 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 chr12:56995426 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 chr12:106632981 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 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 chr13:32914960 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 chr13:103419690 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 chr14:50583165 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 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 chr15:43025296 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 chr15:89873443 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 chr16:49671946 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 chr16:67909845 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 chr16:81249934 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 chr17:10535903 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 chr17:17700284 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 chr17:26820717 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 chr17:35512648 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 chr17:39262230 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 chr17:56349050 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 chr17:78343328 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 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 chr18:44589672 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 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 chr19:20117296 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 chr19:43680124 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 chr19:54667457 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 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 chr2:27016086 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 chr2:74757144 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 chr2:128066316 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 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 chr20:57251298 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 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 chr22:30806615 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 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 chr3:50379108 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 chr3:69027582 G>A maps to ENST00000383701 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A1HR-01A-11D-A13W-08 chr3:109050828 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 chr3:122811200 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 chr3:172643145 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 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 chr4:142147921 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 chr4:183675803 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 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 chr5:38484883 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 chr5:74970316 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 chr5:145239352 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 chr6:24503594 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 chr6:54025593 C>G maps to ENST00000502396 V832V. 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 chr7:127341353 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 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 chr8:54147421 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 chr8:124250181 C>G 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 chr9:125797111 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 chr9:137676851 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 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-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 chr1:54343991 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 chr1:57481003 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 chr1:93677789 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 chr1:112524481 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 chr1:151338295 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 chr1:151506504 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 chr1:152749145 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 chr1:168278088 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 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 chr10:97775977 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 chr10:121156214 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 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 chr11:57080262 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 chr11:64502636 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 chr12:15803940 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 chr12:51845972 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 chr12:112666448 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 chr13:41705449 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 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 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 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 chr16:67695397 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 chr16:71668135 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 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 chr17:59763272 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 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 chr19:40030086 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 chr19:44778141 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 chr19:49692257 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 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 chr2:85097648 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 chr2:128412050 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 chr2:190636561 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 chr2:203650666 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 chr2:241569479 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 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 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 chr22:40066080 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 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 chr3:141162246 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 chr3:184429333 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 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 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 chr5:70786809 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 chr5:154346441 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 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 chr6:35773575 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 chr6:130762700 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 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 chr7:31793150 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 chr7:41739708 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 chr7:92732368 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 chr7:129110494 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 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 chr8:35541108 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 chr8:99961626 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 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 chr9:133927971 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 chr9:135702365 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 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:153128147 G>A maps to NM_000425.3 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:3669320 C>G maps to NM_152492.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:19549913 G>A maps to NM_015047.1 I784I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:186034487 C>T maps to NM_031935.2 H2544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:237060353 C>G maps to NM_000254.2 S1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:237949318 T>A maps to NM_001035.2 S4437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr1:247607345 C>G maps to NM_004895.4 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr10:23399190 G>T maps to ENST00000277598 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr10:26559630 C>A maps to NM_001134366.1 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr10:32311874 C>T maps to NM_004521.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr11:407865 G>C maps to NM_021805.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr11:125448903 C>T maps to ENST00000278903 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr12:20774240 G>A maps to NM_000921.3 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr12:53454001 G>A maps to NM_170754.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr12:56536836 C>G maps to NM_001184796.1 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr13:52952520 G>A maps to NM_018676.3 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr13:79916955 G>C maps to ENST00000438737 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr14:51259485 C>A maps to NM_020921.3 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr14:76045320 G>A maps to NM_017791.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:22382960 C>T maps to NM_001005241.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:43939558 C>T maps to NM_172095.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr15:63986694 G>A maps to ENST00000261887 Q1766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:3025756 G>A maps to NM_004203.4 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:3026844 G>A maps to NM_004203.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:14749054 C>T maps to NM_016561.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:66603972 G>A maps to NM_052999.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:72821413 C>T maps to NM_006885.3 S3587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:87446452 G>C maps to NM_015144.2 S488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr16:89703950 C>T maps to NM_004413.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:1478942 G>C maps to ENST00000382147 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:4080442 G>C maps to NM_016376.3 S919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:7216946 G>A maps to NM_004489.4 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:7976525 C>T maps to NM_001139.2 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:11572853 G>A maps to NM_001372.3 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:61972838 C>T maps to NM_001317.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:65175037 G>A maps to NM_014877.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr17:73892976 G>A maps to NM_173547.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr18:19345736 C>T maps to NM_020774.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:10668239 G>A maps to NM_023008.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:10668296 G>A maps to NM_023008.3 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:11258786 G>T maps to NM_182513.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:12491854 G>C did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:12739531 C>T maps to NM_153358.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:13059905 G>A maps to NM_005053.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:37129761 T>C maps to NM_153257.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:47423516 C>T maps to NM_004491.4 R529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr19:49090663 C>T maps to NM_177973.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr2:182413567 G>A maps to NM_001030311.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:31017810 C>T maps to ENST00000375687 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:47707528 C>T maps to NM_001316.2 Q779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr20:47707557 G>A maps to NM_001316.2 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr21:38600635 G>A maps to NM_006052.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr22:20073686 C>T maps to NM_022720.6 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr22:32160959 G>A did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr3:1424975 G>C did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr3:77614212 G>A maps to ENST00000332191 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr3:128525357 C>T maps to NM_004637.5 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:3416498 C>T maps to NM_198229.2 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:10100689 G>A maps to NM_017491.3 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:11401131 C>T maps to NM_005114.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:90034852 C>G maps to NM_145715.2 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:100510815 C>G maps to ENST00000511045 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:122831315 G>A maps to NM_001130698.1 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:169196558 C>T maps to NM_017631.5 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr4:187518863 G>A maps to ENST00000260147 Q4117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr5:140604576 C>A maps to NM_018934.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr5:140750326 G>A maps to NM_018924.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr5:171471887 A>C maps to NM_005990.3 *969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:46806750 G>T maps to NM_005588.2 E707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:131971179 G>A maps to NM_005021.3 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:132891942 C>A maps to NM_175067.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr6:149700619 G>C maps to NM_015093.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr7:116849887 G>A maps to ENST00000323984 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr8:56675386 G>C maps to ENST00000434581 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr8:124253502 G>T maps to NM_032847.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr9:14674275 G>A maps to NM_178566.4 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr9:15468841 C>G did not map to a codon.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chr9:71990747 C>T maps to NM_001127608.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chrX:123197010 C>T maps to NM_001042750.1 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A27C-01A-11D-A16O-08 chrX:153205629 G>A maps to NM_002910.5 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr1:148015634 A>C maps to ENST00000310701 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr10:118314750 C>T maps to NM_000936.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr12:133732510 C>T maps to NM_015394.4 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr16:67470803 G>A maps to NM_000196.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr17:63532492 G>A maps to NM_004655.3 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr2:174223510 G>A maps to NM_031942.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr20:61525840 G>A maps to NM_033081.2 V832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr20:62730139 G>A maps to NM_000913.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr4:9452167 T>C maps to NM_001040448.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MF-01A-12D-A21A-08 chr6:36652023 G>A maps to ENST00000448526 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:12463959 C>G maps to NM_015378.2 L3988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:40882741 C>T maps to NM_022733.2 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:78267137 A>G maps to NM_198549.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:152286241 C>A maps to NM_002016.1 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:153309654 A>G did not map to a codon.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:155001802 G>A maps to NM_144622.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:166819003 G>C maps to NM_017542.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr1:245849191 G>A maps to NM_018012.3 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr10:26462804 C>T maps to NM_017433.4 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr10:95072941 G>A maps to NM_013451.3 H1908H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr10:106916943 C>T maps to NM_014978.1 Q511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr11:55904465 C>A maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr11:71950870 G>A maps to NM_005169.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:52200726 C>T maps to NM_014191.2 L1819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:57918190 C>G maps to NM_052897.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:67703817 G>T maps to NM_018448.3 E1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr12:121132929 C>G maps to NM_014730.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr13:41133686 T>C maps to NM_002015.3 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr13:95114289 G>A maps to NM_001129889.1 F339F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr13:113052393 G>A maps to NM_145248.4 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr14:71443816 C>T maps to NM_014982.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr15:26792967 A>T maps to NM_021912.4 L465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr15:83776473 C>T maps to NM_023003.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr15:94913371 T>G maps to NM_018349.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr16:732416 C>T maps to NM_005861.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr16:68071988 G>T maps to NM_017803.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:465900 G>A maps to NM_001128159.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:39580631 G>A maps to NM_003770.4 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:42165951 G>A maps to NM_001015053.1 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr17:48941122 G>A maps to NM_005749.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr19:41631522 C>T maps to NM_000774.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr19:54692144 G>A maps to NM_024298.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:63282823 C>T maps to NM_014562.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:65245357 C>G maps to NM_003038.4 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:69759276 C>T maps to NM_014911.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:73160941 G>A maps to NM_004097.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:105900800 G>A maps to NM_004257.4 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:179596191 G>A maps to NM_133378.4 S4523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:202698638 G>C maps to ENST00000450471 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr2:242373631 C>T maps to NM_014808.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr20:35766313 G>A maps to ENST00000343811 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr20:44578440 G>A maps to NM_022095.3 Q1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr20:45850113 G>A maps to ENST00000471951 Q1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr21:30435689 A>G maps to NM_006585.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr21:45170386 G>A maps to NM_003681.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr21:45170411 G>T maps to NM_003681.4 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:17072819 C>T maps to NM_014406.4 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:17976470 C>T maps to ENST00000400579 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:18918707 G>A maps to NM_016335.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:39626221 G>A maps to NM_002608.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr22:51182531 C>T maps to NM_001097.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr3:31638348 C>T maps to NM_178862.1 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr3:43122016 C>A maps to NM_032806.4 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr3:169099219 G>A maps to NM_004991.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr6:110943359 G>A maps to NM_015076.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr6:152461087 G>C maps to NM_182961.2 L8485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr7:128317839 G>A maps to NM_001012454.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr7:142626152 C>A maps to NM_019841.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr8:22033755 G>A maps to NM_006129.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr8:38021253 C>T maps to NM_014462.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr9:33464904 G>C maps to NM_022917.4 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr9:125681288 G>A maps to NM_020924.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chr9:125898321 G>A maps to NM_018387.4 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chrX:9659695 G>T maps to NM_005647.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MG-01A-11D-A20D-08 chrX:140993969 T>C maps to NM_005462.4 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr1:152552262 G>A maps to NM_032563.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr12:4835914 C>G maps to NM_017417.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr12:40499376 G>A maps to NM_052885.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr12:110391019 C>T maps to NM_057169.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr15:41105569 T>C maps to NM_001077268.1 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr19:20728096 C>T maps to NM_001159293.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr19:23927313 G>A maps to NM_138286.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr2:197672316 C>T maps to NM_213608.1 K68K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr2:234183393 G>T maps to ENST00000392018 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr21:31709533 G>A maps to NM_001077711.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr6:133111327 T>C maps to NM_052831.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chr8:110448689 T>C did not map to a codon.
Sequencing variant TCGA-CF-A3MH-01A-11D-A20D-08 chrX:12905874 C>T maps to NM_016562.3 R750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr1:184787959 C>T did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr1:228462330 C>T maps to NM_001098623.1 G1914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr10:15863725 C>T did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr11:4621769 C>G maps to NM_018073.5 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr12:121882332 C>A maps to ENST00000377071 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr16:30794835 G>A maps to NM_001080417.1 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr16:66621937 A>G maps to NM_144673.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:650820 G>A maps to NM_015721.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:8449972 C>T maps to ENST00000360416 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:17083383 C>T maps to NM_015134.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr17:30815243 C>T maps to NM_003885.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr19:630112 C>T maps to NM_005035.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr19:1789015 C>G maps to NM_138813.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr19:19626254 C>T did not map to a codon.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr20:2413264 C>T maps to NM_198994.2 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr20:56093884 G>A maps to ENST00000423479 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr21:34011220 C>T maps to NM_003895.3 P1343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr22:42610591 G>A maps to NM_005650.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr3:49947847 G>A maps to NM_032355.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr3:73433184 G>A maps to NM_015009.1 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:127796587 G>A maps to NM_001012279.2 D861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:147527159 A>G maps to NM_001127715.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr6:152675919 C>T maps to NM_182961.2 L3600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr7:99917268 T>C maps to NM_001004351.4 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:123921141 C>T maps to NM_007018.4 Q1592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:127637309 T>C maps to NM_030978.1 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:131669701 C>T maps to NM_001127244.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:131670420 C>T maps to NM_001127244.1 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chr9:131671080 C>G maps to NM_001127244.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CF-A3MI-01A-11D-A20D-08 chrX:123217379 C>T maps to NM_001042750.1 R1012*. 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 chr1:99772548 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 chr1:181018368 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 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 chr10:21804177 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 chr10:61829046 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 chr11:32635178 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 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 chr12:121706439 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 chr13:48947628 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 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 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 chr17:68171212 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 chr19:2433946 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 chr19:3623700 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 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 chr2:27551029 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 chr2:215854126 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 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 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 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 chr3:150916248 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 chr4:183696287 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 chr5:40843578 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 chr5:150934192 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 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 chr6:147704099 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 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 chr9:137777142 C>A maps to NM_004108.2 T120T. 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 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 chr11:116692359 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 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 chr15:64496767 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 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 chr16:70884497 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 chr17:17080691 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 chr17:78704397 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 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 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 chr20:25666701 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 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 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 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 chr5:78964812 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 chr5:140710505 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 chr6:31498939 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 chr6:151116990 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 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 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-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 chr1:11097836 A>G maps to NM_006610.2 P307P. 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 chr1:64027422 T>C maps to NM_032437.2 F464F. 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 chr1:211529791 T>A maps to ENST00000427925 V120V. 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 chr11:4967691 A>G maps to NM_001005329.1 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 chr11:30033502 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 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 chr12:70672039 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 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 chr16:449377 G>A did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr16:70834773 G>T maps to NM_018052.3 L10L. 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 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 chr19:42260766 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 chr19:49797168 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 chr19:53994028 T>G maps to NM_001004301.3 S181S. 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 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 chr20:31962019 T>G did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr20:33680619 C>T did not map to a codon.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr22:41865167 A>G maps to ENST00000396512 L6L. 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 chr3:40192631 C>T maps to NM_015460.2 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:42577694 G>T maps to NM_004624.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr3:127294259 G>A maps to NM_001136053.1 I253I. 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 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 chr6:17539633 T>C maps to NM_006366.2 S257S. 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 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 chr7:48284187 G>A maps to NM_152701.3 W426*. 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 chr9:88257813 T>C maps to ENST00000395847 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A0YR-01A-12D-A10S-08 chr9:116856477 T>C maps to ENST00000259410 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:3644230 C>T maps to NM_005427.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:31478698 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:104116526 C>T maps to NM_020978.3 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:155989829 C>T maps to ENST00000368312 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:158059547 G>C maps to ENST00000368173 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:167792258 G>T maps to NM_018417.4 I1385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:201749602 C>G maps to ENST00000367296 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr1:240255998 C>G maps to ENST00000406993 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:6261551 G>A maps to NM_004566.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:21102871 G>C maps to ENST00000430741 S783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:43696156 G>A maps to ENST00000374459 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr10:89504907 C>T maps to NM_001015880.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:6220473 C>G maps to NM_001005178.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:18503373 C>A maps to NM_006292.2 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:43333682 G>A maps to NM_001142930.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr11:89924899 G>A maps to NM_005467.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr12:14633974 C>T maps to NM_018179.3 Q1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr12:96368045 C>T maps to NM_002108.2 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:39438669 G>A maps to NM_207361.4 W2637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:45973210 G>C maps to NM_001010875.2 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr13:78477332 T>C maps to ENST00000377211 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:22134222 G>A maps to NM_001001912.1 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:52781490 G>A maps to NM_000956.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:65260361 G>C maps to ENST00000389723 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:86087956 C>G maps to NM_013231.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:86088061 C>G maps to NM_013231.4 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:90650737 C>T maps to NM_022054.2 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr14:100758859 G>A maps to NM_001039355.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:33928728 C>T maps to NM_001036.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:65360143 C>G maps to NM_016563.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:73007668 C>G maps to NM_033028.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr15:79284124 C>T maps to NM_002891.4 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr16:20999095 C>T maps to NM_017539.1 S2267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr16:67331451 C>T maps to NM_001100915.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr16:67685193 C>T maps to NM_001013838.1 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr17:21207741 G>A maps to NM_145109.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr17:77043905 C>T maps to ENST00000392445 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:10073542 G>A maps to NM_015719.3 S1601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:14076444 G>A maps to NM_002918.4 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:42880155 C>T maps to ENST00000251268 V2589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:48634392 G>A maps to NM_000234.1 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr19:53959830 T>C maps to NM_001008401.3 Y690Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:71187067 G>A did not map to a codon.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:125261951 C>T maps to NM_130773.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:137928488 C>T maps to ENST00000272643 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:150071148 G>A maps to NM_177964.3 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr2:202400896 C>T maps to NM_001168221.1 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr20:42825949 C>T maps to NM_016470.6 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr20:62871219 C>T maps to NM_004535.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr21:17250766 C>T maps to ENST00000285681 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr21:43802183 G>C maps to ENST00000380399 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr21:46363636 C>A maps to NM_058190.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:29106035 G>A maps to NM_001005735.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:38266267 G>A maps to ENST00000262832 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41572403 C>T maps to NM_001429.3 R1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41573078 C>G maps to NM_001429.3 L1788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41573837 C>G maps to NM_001429.3 L2041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr22:41573888 C>G maps to NM_001429.3 L2058L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:4711445 G>A maps to ENST00000356617 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:93802970 C>G maps to NM_022072.3 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:107520008 A>G maps to NM_001142568.1 K873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:128356704 G>A maps to NM_002950.3 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr3:185155307 C>T maps to NM_004721.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:9190394 G>T maps to NM_003966.2 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:79026792 G>A maps to NM_153610.3 E735E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:90078971 A>G maps to NM_032119.3 P4421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:140431441 T>C maps to NM_013340.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:140794088 C>T maps to NM_018913.2 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr5:159831860 C>T maps to NM_006425.4 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr6:35928811 G>C maps to NM_052961.3 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr6:45922938 G>A maps to NM_001114086.1 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr6:73843245 C>T maps to NM_001160133.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:6629997 C>T maps to NM_024067.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:24749945 G>C maps to NM_001127453.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:43916934 G>C maps to NM_001077663.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:48080988 G>A maps to ENST00000430738 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:66418352 G>A maps to NM_017994.4 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:90895016 C>T maps to NM_003505.1 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:99686982 C>G maps to NM_006833.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:100483361 C>G maps to NM_015908.5 S453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:143657917 G>A maps to NM_012369.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:148800825 G>A maps to NM_001001661.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr7:148801777 G>A maps to NM_001001661.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr8:23082520 C>G maps to NM_003844.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr8:110984712 C>T maps to NM_014379.2 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr8:145535420 C>T maps to NM_005526.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr9:131745214 C>T maps to NM_015354.1 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chr9:132889829 G>A maps to NM_001136557.1 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chrX:44949016 G>A maps to NM_021140.2 W1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3KJ-01A-11D-A21A-08 chrX:53620498 G>C maps to ENST00000276009 S1189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:1372364 C>T maps to NM_022834.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:12336627 G>T maps to NM_015378.2 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:12918912 C>T maps to NM_023014.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:35853066 C>T maps to NM_005095.2 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:92789859 G>C maps to NM_024813.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr1:163317647 G>A maps to NM_145697.2 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:11362440 G>A maps to NM_198516.2 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:44089203 C>T maps to NM_032592.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:49227725 T>G did not map to a codon.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr11:120998485 C>T maps to NM_005422.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr12:107372069 A>G maps to NM_025198.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr14:24740141 C>T maps to NM_182836.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr15:93540503 C>G maps to NM_001271.3 V1252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:40169377 G>A maps to NM_003315.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:43345028 C>T maps to ENST00000344686 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:73832316 G>A maps to ENST00000412096 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr17:76993383 G>A maps to NM_138793.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:6372968 G>A maps to NM_032306.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:16688391 G>T maps to NM_004831.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:18327577 C>G maps to NM_000923.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:45868142 G>A maps to NM_000400.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:46823769 C>A maps to NM_152795.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr19:49384273 G>A maps to NM_003323.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:103013261 G>A maps to NM_003855.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:107084738 A>G maps to ENST00000304514 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:216249685 C>T maps to NM_212482.1 P1542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr2:242415380 G>A maps to NM_014808.2 E747E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr20:31021690 A>T maps to ENST00000375687 K564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr20:44979475 G>T maps to NM_173179.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:52813597 G>A maps to NM_002215.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:57850349 G>T maps to ENST00000428312 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:129324822 G>A maps to NM_015103.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr3:183368872 G>C maps to NM_017644.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr4:36130167 C>T maps to NM_015230.2 W1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr4:39233497 C>T maps to NM_025132.3 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr4:46737170 G>A maps to NM_130902.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr5:38370442 G>A maps to ENST00000354891 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr5:113698897 C>T maps to NM_021614.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr6:36651905 C>T maps to ENST00000448526 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr7:117232104 G>A maps to NM_000492.3 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr8:38677715 C>G maps to ENST00000379931 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chr9:21239748 G>T maps to NM_002172.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chrX:1409370 C>T maps to NM_001161530.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3QU-01A-11D-A22Z-08 chrX:73751255 C>T maps to NM_006517.3 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:979600 C>G maps to NM_198576.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:16134161 G>C did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:32687560 C>T maps to NM_019118.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:158747278 G>A maps to NM_001005278.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:161697271 G>A maps to NM_001002901.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr1:248487243 G>A maps to NM_001004691.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr10:61830480 C>T maps to NM_020987.2 G3386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr10:81037043 C>G maps to NM_020338.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:1026379 G>A maps to NM_005961.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:6643189 G>A maps to NM_003737.2 I3239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:19209780 G>A maps to NM_003476.3 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:64575137 C>T maps to NM_130804.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr11:124189262 G>A maps to NM_001002918.1 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:6700749 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:40699616 C>T maps to NM_198578.3 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:112843710 C>T maps to NM_001024662.1 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr12:122199640 C>G maps to NM_001080825.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr13:49796425 G>A maps to NM_001507.1 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr14:61517299 G>A maps to NM_001172702.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr14:88693730 C>T maps to NM_138318.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr15:49148319 C>A maps to NM_203349.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr15:63908119 C>G did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:53524210 G>A maps to NM_005611.3 *1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:67324841 G>A maps to NM_001100915.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:75579303 C>G maps to NM_001077416.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:75663369 C>T maps to NM_001130089.1 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr16:89929915 G>C maps to NM_032451.1 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:3854916 G>A maps to NM_174953.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:15960869 G>C maps to ENST00000395857 S2132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:46862466 C>A maps to NM_001130918.1 E620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:54671874 C>A maps to NM_005450.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr17:74737111 C>T maps to NM_024311.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr18:61647087 C>T maps to NM_198833.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:1255045 C>G maps to NM_177401.4 S281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:16902159 G>C did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:33467383 G>A maps to NM_152266.3 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:39955604 C>G maps to NM_003169.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:45976194 C>T maps to NM_006732.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:51857427 G>A maps to NM_001014763.1 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:53678788 G>A maps to NM_024733.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:58549426 G>T maps to NM_182572.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr19:59057193 C>T maps to NM_005762.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:26739407 G>A maps to NM_194248.2 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:27850501 C>T maps to ENST00000435516 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:36994238 G>T maps to NM_053276.3 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:50724723 C>A maps to ENST00000404971 G916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:68607461 G>C maps to NM_002664.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:130910918 G>A maps to NM_017951.4 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr2:201873709 G>A maps to NM_173822.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr20:3888747 C>T maps to NM_153638.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr22:23406201 G>T maps to NM_014433.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr22:50187865 G>A maps to ENST00000342989 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:7503405 C>G maps to NM_181874.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:32933230 C>T maps to NM_001039111.1 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:33416784 C>T maps to NM_012157.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:49062586 C>T maps to NM_000884.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr3:126708281 C>T maps to NM_032242.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr4:56284048 T>A maps to NM_018475.3 L230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:14358312 G>A maps to NM_007118.2 Q691Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:66460280 C>G maps to NM_001164664.1 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:110407680 C>T maps to NM_033035.4 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr5:161528315 C>T maps to NM_198903.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr6:125578273 G>A maps to NM_003287.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr7:77200496 C>T maps to NM_002835.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr7:97619395 G>A maps to NM_006188.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr7:148802518 G>C maps to NM_001001661.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:17507471 C>T did not map to a codon.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:99468129 C>T maps to ENST00000354930 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:124371476 T>A maps to NM_014109.3 K456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr8:144993272 G>A maps to NM_201380.2 I3709I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr9:102590461 G>A maps to NM_173200.1 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr9:131396646 G>A maps to NM_052844.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chr9:140695357 C>T maps to NM_024757.4 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CU-A3YL-01A-11D-A22Z-08 chrX:3238722 G>C maps to NM_015419.3 S1668*. 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 chr1:7907828 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 chr1:22924701 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 chr1:27695778 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 chr1:36181307 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 chr1:38197173 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 chr1:45269323 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 chr1:59142622 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 chr1:84867739 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 chr1:110466436 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 chr1:114524372 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 chr1:155177628 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 chr1:169494147 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 chr1:202935921 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 chr1:207228121 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 chr1:213032135 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 chr1:229771853 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 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 chr10:97376260 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 chr10:103900463 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 chr10:112839121 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 chr10:135213088 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 chr11:5444185 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 chr11:59349007 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 chr11:116640939 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 chr11:120008355 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 chr11:124949112 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 chr11:130785627 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 chr12:12630909 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 chr12:29757223 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 chr12:41967406 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 chr12:49890686 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 chr12:54423559 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 chr12:56536447 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 chr12:58114291 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 chr12:90005095 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 chr12:102559616 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 chr12:112477110 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 chr12:120221777 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 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 chr13:111973257 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 chr14:45542645 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 chr14:75231007 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 chr14:104121149 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 chr15:52553306 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.
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 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 chr16:30735079 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 chr16:50339494 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 chr16:50383963 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 chr16:84473070 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 chr17:4086694 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 chr17:6930282 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 chr17:7217446 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 chr17:7578274 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 chr17:26856165 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 chr17:40070072 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 chr17:48434546 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 chr17:65141897 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 chr17:73017051 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 chr17:74387281 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 chr18:51731412 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 chr19:2987902 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 chr19:6177389 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 chr19:8136969 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 chr19:12060203 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 chr19:17213294 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 chr19:17440785 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 chr19:18963839 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 chr19:34818938 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 chr19:37382766 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 chr19:40480724 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 chr19:53383881 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 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 chr2:31572631 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 chr2:38893362 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 chr2:43458298 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 chr2:74708005 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 chr2:96992596 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 chr2:103236426 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 chr2:152127233 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 chr2:198380839 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 chr2:219498428 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 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 chr20:40065974 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 chr20:47704591 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 chr20:51871959 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 chr20:62838959 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 chr22:36681273 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 chr22:50928200 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 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 chr3:42777312 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 chr3:53159983 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 chr3:100354654 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 chr3:121416387 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 chr3:129288722 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 chr3:134967279 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 chr3:159995412 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 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 chr4:79238533 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 chr4:107249296 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 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 chr5:45462007 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 chr5:102442446 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 chr5:134332198 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 chr5:156932735 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 chr5:167993163 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 chr6:18122785 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 chr6:26501555 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 chr6:27833491 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 chr6:32134564 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 chr6:33284429 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 chr6:46658619 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 chr6:94068096 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 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 chr7:44579101 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 chr7:117400555 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 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 chr8:21997684 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 chr8:61748693 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 chr8:109797207 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 chr8:139629180 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 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 chr9:97082699 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 chr9:129157917 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 chr9:135781418 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 chr9:137804335 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 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: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 chr1:22828865 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 chr1:50610765 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 chr1:54060248 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 chr1:94476480 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 chr1:145586853 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 chr1:155020371 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 chr1:238048518 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 chr1:248685405 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 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 chr11:49176029 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 chr11:59224918 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 chr11:89424063 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 chr12:26875356 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 chr12:71833916 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 chr12:120263154 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 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 chr14:63269242 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 chr14:68043122 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 chr15:85401088 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 chr16:20430711 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 chr16:72923774 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 chr17:18498090 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 chr17:67178945 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 chr17:79165120 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 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 chr19:16001183 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 chr19:49558232 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 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 chr2:219679422 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 chr2:220466158 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 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 chr20:50049279 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 chr20:62324318 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 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 chr22:32924938 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 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 chr3:36872832 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 chr3:40457434 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 chr3:160156350 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 chr4:22449099 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 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 chr5:150666827 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 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 chr6:46214587 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 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 chr7:81388060 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 chr7:99710523 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 chr7:135263631 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 chr7:150390121 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 chr8:125568499 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 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 chr9:140707936 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 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:99663457 C>T maps to NM_001184880.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:10720281 G>A maps to NM_001079843.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:26772805 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:29438878 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:35656102 G>A maps to NM_005066.2 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:43394662 G>A maps to NM_006516.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:55277825 G>C maps to NM_001110533.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:104160107 C>T maps to NM_000699.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:111966265 G>A maps to ENST00000369728 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:152276030 C>T maps to NM_002016.1 S3777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:153920994 G>A maps to NM_181715.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:159683509 G>A maps to NM_000567.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:169511936 G>C maps to ENST00000367796 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:205042278 C>T maps to NM_005076.3 D976D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr1:220364530 G>A maps to ENST00000358951 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:43088105 G>A maps to NM_006955.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:69925570 G>C maps to NM_032578.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:75279709 C>A maps to NM_152586.3 T841T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:87373286 G>C maps to NM_017551.2 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:98762696 G>A maps to NM_003061.2 N1306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr10:98823296 G>A maps to NM_003061.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:17409305 G>A maps to NM_000525.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:32997930 C>T maps to NM_001076786.1 Q1707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:44089397 G>A maps to NM_032592.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:57106038 C>T maps to NM_002559.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:66407490 G>A maps to NM_002896.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:77907437 C>T maps to NM_020798.2 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr11:94194100 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:51757939 C>T maps to NM_007210.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:97051868 C>T maps to ENST00000342887 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:112182843 C>T maps to NM_001136538.1 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:113705697 C>T maps to NM_001143819.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:125396364 C>T maps to NM_021009.5 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr12:132203997 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr13:29008207 G>C maps to NM_002019.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr13:110435066 C>A maps to NM_003749.2 E1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr14:88938709 G>A maps to NM_007039.3 R917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:22383191 C>T maps to NM_001005241.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:52672021 G>C maps to ENST00000358212 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:84611708 C>T maps to NM_207517.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr15:88678347 G>A maps to NM_001012338.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:19125971 C>A maps to NM_001034841.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:28925597 G>A maps to NM_024816.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:30004528 C>T maps to NM_003609.3 *557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr16:58538304 C>G maps to NM_001130487.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:16526921 C>T maps to NM_020787.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:16527692 C>T maps to NM_020787.3 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:64049895 C>T maps to NM_145036.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:72767985 G>A maps to NM_015654.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr17:72888658 G>A maps to ENST00000310226 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr18:18622099 G>C maps to NM_005406.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:2222098 C>T maps to ENST00000221482 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:17039044 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:17166704 G>A maps to NM_033417.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:18546113 C>A maps to NM_016368.4 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:38860867 C>T maps to NM_021185.4 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:43376147 C>T maps to NM_006905.2 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:46522874 G>A maps to NM_005091.2 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:56244155 C>T maps to NM_176820.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr19:58724433 C>A maps to NM_133502.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:120204400 G>A maps to NM_002980.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:165365356 C>T maps to NM_004490.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:168103463 G>A maps to NM_152381.5 Q1854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:220353542 C>T maps to NM_005876.4 Y2690Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr2:223168710 G>A maps to NM_153038.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:8678318 G>C maps to NM_015192.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:30784257 C>T maps to NM_002657.3 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:45633579 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:61981889 G>C maps to NM_000744.5 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr20:62421702 G>A maps to NM_025224.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr21:47531977 C>G maps to NM_001849.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:17072000 C>T maps to NM_014406.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:19870907 C>T maps to NM_006440.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:20100674 G>A maps to ENST00000439169 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr22:50962177 G>T maps to NM_001169111.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr3:10354377 G>A maps to ENST00000343726 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr3:119209462 C>A maps to NM_152305.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr3:182759418 T>C maps to NM_020166.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:8284260 G>A maps to NM_053044.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:25351118 C>T maps to NM_024936.2 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:42403227 C>T maps to NM_001080505.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:46043249 C>A maps to NM_173536.3 G385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr4:146063357 A>G maps to ENST00000447906 F604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:13913869 G>A maps to NM_001369.2 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:140024594 C>G maps to ENST00000252100 S471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:140725378 G>A maps to NM_018916.3 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:169507183 G>A maps to NM_004946.2 E1728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr5:179666935 C>A maps to NM_002752.4 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:10410426 G>A maps to ENST00000379613 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:28891283 G>A maps to NM_006510.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:29408454 C>A maps to NM_013941.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:33257969 G>A maps to NM_001185181.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr6:153043096 G>C maps to NM_025107.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:4051843 G>T maps to NM_152744.3 G799G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:16745683 G>C did not map to a codon.
Multiple mappings detected for codon TCGA-DK-A1A6-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:63673567 A>G maps to NM_001159524.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:86468799 C>G maps to NM_000840.2 S657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:87913436 G>A maps to NM_024636.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr7:158824560 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:385663 C>G maps to NM_183421.1 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:21840320 G>A maps to ENST00000434536 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:22035398 G>A maps to NM_006129.4 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:68931793 C>G maps to NM_024870.2 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr8:133844493 G>T maps to ENST00000395386 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:8521490 T>A maps to NM_002839.3 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:27169598 C>T maps to NM_000459.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:131346652 C>T maps to NM_001130438.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chr9:131347040 C>T maps to NM_001130438.2 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chrX:34148658 G>A maps to NM_203408.3 Y579Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chrX:40540141 C>A maps to NM_004229.3 S826S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chrX:53578102 C>T maps to ENST00000276009 Q3050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chrX:54957053 C>T maps to NM_001039705.1 F1299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chrX:100086568 C>A maps to ENST00000415585 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1A6-01A-11D-A13W-08 chrX:151092369 C>T maps to ENST00000427663 F106F. 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 chr1:36941191 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 chr1:159842831 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 chr1:203667471 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 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 chr10:120817658 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 chr10:135011910 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 chr11:102495963 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 chr12:72680476 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 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 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 chr15:76994115 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 chr16:74685991 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 chr17:56774140 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 chr18:31318936 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 chr19:33663288 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 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 chr2:171700563 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 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 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 chr22:41928096 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 chr22:50563823 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 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 chr3:121994735 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 chr3:136287646 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 chr3:151046555 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 chr4:56471507 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 chr4:144127184 G>A did not map to a codon.
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 chr5:177637273 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 chr6:32808758 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 chr6:33245679 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 chr6:87970339 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 chr6:160483634 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 chr7:6210830 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 chr7:133884159 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 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 chr9:131329129 T>C maps to NM_001130438.2 R37R. Only missense variants will be evaluated by CHASM.
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: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-A1AA-01A-11D-A13W-08 chr1:118476013 T>G maps to NM_006784.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr1:158064738 C>T maps to ENST00000368173 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr10:105128036 A>G maps to NM_006951.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr11:117253628 C>T maps to NM_014956.4 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr12:57637893 G>A maps to NM_145064.1 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr12:95434301 C>A maps to NM_003297.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr16:2121803 G>T maps to NM_000548.3 E656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr16:28112859 G>A maps to NM_015171.2 F1065F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr19:14070851 C>T maps to NM_138353.2 F499F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr19:44222904 G>A maps to NM_019612.3 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr19:55377273 C>T maps to ENST00000355608 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr2:112944788 C>A maps to NM_153214.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr2:210962865 T>G maps to NM_152519.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr3:38565703 C>T maps to NM_005107.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr4:1656881 G>A maps to NM_001174070.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr4:122740026 G>C maps to NM_001237.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr5:94858954 G>A maps to NM_014639.3 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr6:32024426 C>T maps to ENST00000375244 K2693K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr6:51497480 C>T maps to NM_138694.3 L3849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr6:51497482 A>G maps to NM_138694.3 L3849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr7:42950478 G>A maps to NM_001099858.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr8:26365182 G>A maps to NM_007257.5 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chr8:116599371 C>A maps to NM_014112.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chrX:44913156 G>T maps to NM_021140.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chrX:122753269 G>C maps to NM_001081550.1 L1431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AA-01A-11D-A13W-08 chrY:15591421 C>A maps to NM_007125.3 E42*. 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 chr1:151491774 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 chr1:168014276 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 chr1:229773863 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 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 chr10:92617281 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 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 chr11:61254052 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 chr11:72145374 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 chr12:27573405 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 chr12:49230567 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 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 chr14:39783994 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 chr14:50472343 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 chr14:102442047 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 chr15:29393869 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 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 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 chr17:7578187 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 chr17:62020201 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 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 chr19:42848851 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 chr19:45285643 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 chr19:51361377 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 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 chr2:54874296 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 chr2:118582551 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 chr2:179481948 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 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 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 chr3:73114034 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 chr3:127295477 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 chr3:136045669 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 chr4:10083019 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 chr4:68619663 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 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 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 chr6:32017874 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 chr7:17378910 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 chr8:59494244 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 chr8:100904265 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 chr8:113348980 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 chr9:133780648 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 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:139865961 G>A maps to NM_004065.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:1226988 G>A maps to NM_001130413.2 *705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:1290311 G>A maps to NM_032348.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:1334488 C>T maps to NM_030937.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:2125481 C>T maps to ENST00000359030 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:2268253 G>A maps to NM_024848.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:3547607 G>A maps to NM_017818.3 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:6195342 G>A maps to NM_015557.2 N939N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:6696216 C>T maps to NM_018198.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:9613858 C>T maps to NM_032315.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:10067688 G>A maps to ENST00000377192 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:11882770 G>A maps to ENST00000376496 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:12304592 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:12387711 G>A maps to NM_015378.2 L2666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:15956938 C>T maps to NM_032341.4 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:16259145 G>A maps to NM_015001.2 L2137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:16269162 C>T maps to ENST00000375733 V633V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:19186031 G>C maps to NM_152232.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:22178311 A>T maps to NM_005529.5 T2326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:23696056 G>A maps to ENST00000507744 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:24768669 C>T maps to NM_020448.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:27121286 C>T maps to NM_017837.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:27124266 C>T maps to NM_017837.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:28206494 C>T maps to NM_001105556.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:33245124 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:33252625 C>T maps to NM_003680.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:35476589 C>T maps to NM_007167.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:36181316 G>A maps to NM_152374.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:39352268 C>T maps to ENST00000372985 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:40041524 G>A maps to NM_001135653.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:41283960 C>T maps to NM_004700.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:43213044 G>A maps to NM_022356.3 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:47024306 C>T maps to NM_003684.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:47564902 G>A maps to NM_178134.2 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:52805845 G>A maps to NM_004799.2 V1294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:54428057 C>T maps to NM_052940.3 C301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:57320597 C>T maps to NM_000562.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:63920111 G>A maps to ENST00000371092 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:64643415 C>T maps to NM_005012.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:79385972 G>A maps to NM_022159.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:89477537 G>A maps to NM_018284.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:92941705 G>A maps to NM_005263.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:94033312 G>A maps to NM_003567.2 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:94048274 G>A maps to NM_003567.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:94370096 G>A maps to NM_002061.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:107600218 G>A maps to NM_018137.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:112299298 G>A maps to NM_007204.4 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:116245547 G>A maps to NM_001232.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:144952286 C>T maps to NM_014644.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:145562891 T>G maps to NM_144698.3 Y860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:145688150 G>A maps to NM_014455.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:150193048 G>A maps to NM_030920.3 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:150550773 G>A maps to NM_021960.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151021022 C>T maps to NM_017860.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151339219 G>A maps to ENST00000435071 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:151785507 G>T maps to ENST00000392697 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:152083963 G>A maps to NM_007113.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:152276090 G>A maps to NM_002016.1 T3757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:154988998 C>T maps to ENST00000417934 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:155161823 G>A maps to ENST00000425082 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:155823270 G>A maps to ENST00000368331 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156051411 C>T maps to NM_001093725.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156256051 G>A maps to NM_032323.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156263940 C>T maps to NM_144580.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156280782 C>T maps to NM_005998.4 Q453Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:156354597 G>A maps to NM_020407.3 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:160681498 G>A maps to NM_001778.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161641317 C>G maps to NM_004001.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161641407 C>T maps to NM_004001.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161695647 C>T maps to NM_001002901.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:161696694 C>T maps to NM_001002901.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:169351513 G>T maps to NM_003666.2 E338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:173916677 G>A maps to NM_172071.2 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:180080148 G>A maps to NM_014810.4 E3069E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:186946810 G>T maps to NM_024420.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:198288555 T>G maps to NM_133494.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:204125004 G>A maps to NM_000537.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:205498222 C>T maps to NM_212503.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:205767809 G>A maps to NM_173854.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:228582711 C>T maps to NM_145214.2 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:230845939 C>T maps to NM_000029.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:236228223 G>A maps to NM_002508.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr1:248039262 C>T maps to NM_015431.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:5009207 C>T maps to NM_001353.5 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:13708120 G>A maps to NM_018027.3 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:20436812 C>T maps to NM_032812.7 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:35894524 C>T maps to NM_153368.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:43612093 C>T maps to NM_020975.4 G733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:48416477 C>G maps to NM_016204.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:63700147 C>T maps to NM_032199.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:75567513 G>C maps to NM_003635.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:88696505 C>T maps to NM_024756.2 K948K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:95400232 G>C maps to NM_006204.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:96698471 C>G maps to NM_000771.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:97607264 C>T maps to NM_001098175.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:97964289 C>T maps to NM_013314.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:98144395 G>A maps to NM_012465.3 F714F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:100022548 G>A maps to NM_032211.6 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:101959726 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:103588902 G>A maps to NM_014591.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:104679814 C>T maps to NM_017649.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:111881974 G>A maps to NM_016824.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:116593032 C>T maps to NM_020940.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:119799771 G>A maps to ENST00000369199 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:120928688 C>T maps to NM_006793.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr10:126172786 C>T maps to NM_022126.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:703074 C>T maps to ENST00000449452 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:1081799 G>A maps to ENST00000441003 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:1856334 G>A maps to NM_138567.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:3707309 G>C maps to NM_016320.4 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:4661060 C>G maps to NM_001004751.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:5624475 G>A maps to NM_001003819.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:5624859 C>G maps to NM_001003819.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:6632653 C>T maps to NM_006284.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:6648800 C>G maps to NM_003737.2 L1823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:9424907 G>C maps to NM_006391.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:9597433 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:10822516 G>A maps to ENST00000429377 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:34680083 G>A maps to NM_012153.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:46563760 G>A maps to ENST00000458649 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:46749599 C>T maps to NM_000506.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:47354824 G>A maps to ENST00000399249 L1084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:47433960 G>A maps to NM_001128225.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:56237064 G>A maps to NM_001004742.1 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:56237766 C>T maps to NM_001004742.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:57243798 C>T maps to NM_178570.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:58940199 G>A maps to NM_015177.1 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:60781006 C>T maps to NM_006725.3 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:62297472 T>C maps to NM_001620.1 T1472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:62372640 G>C maps to ENST00000278845 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:63668427 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64054073 G>A maps to NM_001170726.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64067111 A>C maps to ENST00000422670 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64571922 C>T maps to NM_130804.2 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:64577194 G>A maps to NM_130804.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:65147002 G>A maps to NM_182556.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:65401670 G>A maps to NM_032223.2 L1515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:65812871 G>A maps to NM_033036.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:67051767 C>T maps to NM_001619.3 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:68747723 G>A maps to NM_198923.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:69458748 C>T maps to NM_053056.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:76255316 C>T maps to ENST00000393457 H909H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:77301510 C>T maps to NM_173039.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:85396453 G>A maps to NM_152723.1 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:94113881 G>A maps to NM_016540.3 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:104899925 C>A maps to NM_033292.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:111614219 G>A maps to NM_181699.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:111753252 G>T maps to NM_022761.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:113651191 G>A maps to NM_001101389.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:119181551 G>A maps to NM_006500.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr11:121460046 G>A maps to NM_003105.5 W1342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-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-A1AC-01A-11D-A13W-08 chr11:134014687 G>A maps to NM_032801.3 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:2968484 C>T maps to NM_202002.1 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:6926359 G>T maps to NM_000616.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:12871769 C>T maps to NM_004064.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:20864430 C>A maps to NM_017435.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:33592423 G>A maps to NM_198992.3 L12L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1AC-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:49391910 G>A maps to NM_015086.1 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:49445263 G>C maps to NM_003482.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:51450270 C>T maps to ENST00000448283 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:52827959 C>G maps to ENST00000252245 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53565115 C>G maps to NM_015989.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53607343 G>A maps to NM_000966.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53609124 G>A maps to NM_000966.4 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:53776402 C>T maps to NM_138473.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:55846761 C>T maps to NM_054105.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:56397730 G>C maps to NM_001032387.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:56531078 G>A maps to NM_001184796.1 E630E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:56722296 G>A maps to NM_001127460.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:58127920 G>A maps to NM_001122772.1 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:62861091 C>T maps to ENST00000393630 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:70760747 C>T maps to NM_014505.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:76788452 C>T maps to NM_020841.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:96382018 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:102091701 G>A maps to NM_020244.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:109526079 G>A maps to NM_001145375.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:113737680 G>A maps to NM_024959.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:116418743 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:118511774 C>T maps to NM_019086.5 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:120903590 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:120995411 G>A maps to ENST00000458409 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:121615002 C>T maps to NM_002562.5 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:122817643 C>G maps to ENST00000302528 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:123089503 C>G maps to NM_014708.4 L1752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:123214721 G>A maps to NM_032554.3 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:125398074 C>T maps to NM_021009.5 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:132322756 C>T maps to NM_016155.4 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:133226442 C>T maps to ENST00000455752 P1208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr12:133294682 C>T maps to NM_001170543.1 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:20425495 A>G maps to NM_001142684.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:21751240 C>T maps to NM_024026.4 H62H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:36909156 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:45147905 G>A maps to NM_183422.2 Q769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:45149589 C>T maps to NM_183422.2 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:49085971 G>A maps to NM_001268.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:52548419 C>T maps to NM_000053.2 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:72134057 G>T maps to ENST00000359684 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:77459557 C>T maps to NM_138444.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:77651515 G>A maps to NM_015057.4 L3831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr13:113976672 C>T maps to NM_005561.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:20781942 G>C maps to NM_182849.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:21699231 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:24617579 G>A maps to NM_017999.4 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:24656969 G>T maps to ENST00000458132 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:24772311 C>T maps to NM_174913.1 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:27064679 A>G maps to ENST00000449198 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:38060824 C>T maps to NM_004496.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:45605470 G>A maps to NM_020937.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:52936857 C>T maps to NM_020784.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:61285475 C>T maps to NM_002431.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:65009222 C>T maps to NM_021979.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:91196426 G>A maps to NM_001010854.1 F230F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:101012851 C>G maps to NM_020836.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:103593906 C>T maps to NM_006291.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:103969476 G>T maps to ENST00000335102 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:104571062 C>T maps to NM_001080464.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr14:105618507 G>A maps to NM_002226.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:33941337 G>T maps to NM_001036.3 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:35230974 C>T maps to NM_014691.2 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:40396421 G>A maps to NM_001003940.1 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:40763861 C>G maps to NM_130468.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:43476561 G>A maps to NM_024956.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:45386348 C>T maps to NM_014080.4 *1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:45445632 C>T maps to NM_175940.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:57565344 C>T maps to NM_207036.1 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:59942968 G>A maps to NM_004492.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:64017670 G>A maps to ENST00000261887 Q1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:64332446 G>C maps to NM_014326.3 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:64445457 G>A maps to NM_024798.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:65890801 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:69080225 C>T maps to NM_006305.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:69327704 C>T maps to NM_024505.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:72668265 G>A maps to ENST00000457859 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:75198698 G>A maps to NM_020447.3 H74H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:75335822 C>T maps to NM_021823.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:75499995 C>G maps to NM_015492.4 S536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:78393320 C>T maps to NM_001101404.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:82336487 G>A maps to NM_032246.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:85186741 G>A maps to NM_032856.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:89182686 C>T maps to NM_002201.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:89401275 G>A maps to NM_013227.3 T1820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr15:101718243 C>T maps to NM_014918.4 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:2215899 C>T maps to NM_032271.2 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:8941603 C>T maps to NM_000303.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:15841994 C>A maps to NM_001040114.1 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:16215926 C>T maps to ENST00000399408 V1172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:19041667 G>A maps to NM_024847.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:21214521 C>T maps to NM_003460.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:24817005 G>A maps to NM_014494.2 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:28975090 C>G maps to NM_032815.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:30740402 C>T maps to NM_006662.2 F1925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:31088002 G>T maps to NM_014699.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:31090755 C>T maps to NM_014699.3 C1037C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:46649951 G>A maps to NM_024745.4 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:57016075 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:70301625 G>A maps to ENST00000418685 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr16:83817066 C>T maps to ENST00000268613 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:4045889 G>A maps to NM_015113.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:4577934 C>T maps to ENST00000301396 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:5418328 C>T maps to NM_033004.3 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7256380 G>A maps to NM_001002914.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7492784 C>T maps to NM_006942.1 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7572985 G>A maps to NM_001126112.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7702524 C>T maps to NM_020877.2 I2888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:7760450 G>A maps to NM_032356.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:8725948 G>A maps to NM_001010855.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:26696646 G>C maps to NM_000638.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:26967621 C>T maps to NM_014680.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:27438548 G>A maps to NM_078471.3 H931H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:28770947 C>T maps to NM_001304.4 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:33288629 G>A maps to NM_052857.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:35297718 C>T maps to NM_005568.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:36486037 C>T maps to ENST00000398597 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:39183284 C>T maps to NM_031957.1 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:39190695 C>T maps to NM_030966.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:39551520 G>A maps to ENST00000393998 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:40069976 C>T maps to ENST00000401700 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:40689535 G>A maps to NM_000263.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:41116251 G>A maps to NM_001136042.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:42274333 G>A maps to NM_020218.1 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:42513872 G>C maps to NM_001002909.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:42745072 G>C maps to NM_001145080.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:43226865 C>T maps to NM_006460.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:46805664 C>T maps to NM_006361.5 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:48618873 G>A maps to NM_017957.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:48917452 C>T maps to NM_175575.5 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:56620914 C>T maps to NM_001038704.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:59067591 G>A maps to ENST00000407086 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:66267781 C>T maps to NM_004694.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:67149525 C>A maps to NM_080282.3 L1352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:67170478 T>C maps to NM_080282.3 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:70119039 C>T maps to NM_000346.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:74053482 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:77758612 G>A maps to NM_005189.2 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:79478271 G>A maps to NM_001614.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:79503669 C>G maps to NM_001077182.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:79803466 G>A maps to NM_000918.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:80018632 C>T maps to NM_022156.3 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:80019229 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr17:80574487 G>A maps to NM_019613.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:2920389 G>A maps to NM_014646.2 L864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:8824702 G>A maps to ENST00000456698 V1384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:9522254 G>A maps to NM_006788.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:20606178 A>C maps to ENST00000360790 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:21148934 C>T maps to NM_000271.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:29617111 G>A maps to NM_017831.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:60985641 G>A maps to NM_000633.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr18:77211715 G>A maps to NM_172387.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:1453565 G>A maps to NM_005883.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:2208971 C>T maps to ENST00000221482 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:3964646 G>A maps to NM_001348.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:6187357 G>A maps to NM_030924.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:6829859 C>T maps to NM_005428.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:7184522 G>A maps to NM_000208.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:7743013 C>G maps to NM_174918.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:9677728 G>A maps to NM_001008727.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:10488944 G>A maps to NM_003331.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:10571771 C>T maps to NM_001111307.1 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:10793286 G>A maps to NM_017620.2 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:11040317 G>A maps to NM_138358.2 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:11493834 G>A maps to NM_000121.3 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:12958497 G>A maps to NM_014975.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:13246851 C>T maps to NM_052876.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:13470506 C>T maps to NM_023035.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:15648196 C>T maps to NM_173483.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:16535905 G>A maps to ENST00000455140 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:17339097 G>T maps to NM_024578.1 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:17942578 C>T maps to NM_000215.3 E903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:19359534 G>T maps to NM_004386.2 E1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:19420948 G>A maps to NM_172231.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:33467473 C>T maps to NM_152266.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:33579136 C>T maps to NM_018025.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:35175769 G>A maps to ENST00000221282 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:35512679 G>A maps to NM_020895.3 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:39734755 C>T maps to ENST00000392072 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:39868129 G>A maps to NM_018028.2 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:39926339 C>T maps to NM_001020.4 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:40715100 C>T maps to NM_002446.3 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:41008758 G>A maps to NM_020971.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:41118027 G>A maps to ENST00000308370 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:41349838 G>A maps to NM_000762.5 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:42854307 C>T maps to ENST00000251268 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:43428960 C>T maps to NM_002783.2 *420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:44302739 C>T maps to NM_001031749.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:44676254 C>T maps to NM_001032372.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:46271355 G>A maps to NM_175875.4 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:49334954 C>T maps to NM_016246.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:50393763 C>T maps to NM_172374.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:51527532 G>T maps to NM_144947.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:51920199 C>T maps to NM_033130.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52498045 G>A maps to ENST00000354939 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52568425 G>A maps to NM_001136499.1 N903N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52618286 G>A maps to NM_178523.3 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:52663829 G>A maps to NM_001102657.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:53014287 C>G maps to NM_001099694.1 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:53656991 G>A maps to NM_001172674.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54628016 C>T maps to NM_015629.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54649695 G>T maps to NM_014516.3 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:54666431 G>A maps to NM_001145303.1 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-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-DK-A1AC-01A-11D-A13W-08 chr19:54973371 G>A maps to NM_198988.1 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:55508801 G>A maps to NM_017852.3 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:55912935 G>A maps to NM_014501.2 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:57132855 C>G maps to NM_021216.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr19:58452321 G>A maps to NM_005773.2 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:9540886 G>A maps to NM_003887.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:9695719 G>A maps to NM_003183.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:10101493 C>T maps to NM_198182.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:21233208 A>G maps to NM_000384.2 Y2177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:21233217 C>T maps to NM_000384.2 L2174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:24236210 G>A maps to ENST00000338315 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:25047258 C>T maps to NM_004036.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:27430495 G>T maps to NM_021095.2 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:28152707 A>G maps to NM_004899.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:29295004 G>C maps to NM_001029883.1 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:29354253 T>C maps to ENST00000379543 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:31587028 G>A maps to NM_000379.3 Q876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:32743449 C>T maps to NM_016252.3 Q3827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:38960688 C>T maps to NM_138801.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:54028616 G>A maps to NM_015701.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:54882284 C>T maps to NM_003128.2 F1967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:55252387 G>C maps to NM_020532.4 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:60688924 G>C maps to NM_022893.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:64796343 C>T maps to ENST00000422803 R736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:85108115 G>C maps to ENST00000409520 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:95940392 G>A maps to NM_144707.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:95940455 C>T maps to NM_144707.2 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:96072878 G>T maps to NM_016044.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:97215119 C>T maps to NM_212481.1 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:99984992 G>A maps to NM_015904.3 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:112751898 G>A maps to NM_006343.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:125504878 G>T maps to NM_130773.2 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:136743011 C>T maps to NM_001349.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:149226995 C>G maps to ENST00000404807 S495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:170148822 G>A maps to NM_004525.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:171913056 G>C maps to ENST00000360843 S179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:182766800 C>T maps to NM_001130445.1 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:201342725 C>G maps to ENST00000409151 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:214174841 C>T maps to NM_024532.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:219602554 C>T maps to NM_014640.4 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:220085579 G>A maps to NM_024085.3 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:242135137 G>T maps to NM_001001891.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr2:242163166 C>T maps to NM_001001891.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:947850 G>A maps to NM_001029871.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:2413154 C>T maps to NM_198994.2 Q663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:2968990 G>A maps to NM_002836.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:3891267 G>A maps to NM_153638.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:10625511 C>T maps to NM_000214.2 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:17479525 G>A maps to NM_001195.3 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:17950540 C>G maps to NM_052865.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:18162454 C>T maps to NM_020536.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:24994204 G>A maps to NM_032501.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:30037946 C>A maps to NM_153324.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:30309931 C>T maps to NM_138578.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:32005553 C>T maps to NM_003098.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:33533874 G>A maps to NM_000178.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:33591401 G>C maps to NM_015638.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:33872045 G>A maps to NM_002212.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:35627226 G>A maps to NM_002895.2 Q1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:37576604 G>A maps to NM_030919.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:43571785 C>T maps to NM_006809.4 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:48466214 C>T maps to ENST00000417961 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:48808496 G>A maps to NM_005194.2 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:49212712 C>T maps to NM_080829.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:50401019 C>T maps to NM_020436.3 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:52788163 T>C maps to NM_000782.4 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:56993381 C>T maps to NM_004738.4 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:60893545 G>A maps to NM_005560.3 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:60908289 G>A maps to NM_005560.3 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr20:62340318 G>A maps to NM_032527.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:15599289 G>A maps to NM_144770.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:15599415 G>A maps to NM_144770.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:16339705 G>A maps to NM_003489.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:35895990 G>C maps to NM_004414.5 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:37642412 C>T maps to NM_005128.2 Q1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:40191550 G>A maps to NM_005239.4 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:43867302 G>T maps to NM_018961.2 *662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:45503017 G>C maps to NM_003274.4 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr21:45503078 C>T maps to NM_003274.4 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:18566436 G>A maps to NM_017929.5 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:19418987 C>T maps to NM_003325.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:25747767 A>T maps to NM_001135772.1 *253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:31738884 G>A maps to NM_014323.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:32495202 C>T maps to NM_000343.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:36122284 G>A maps to NM_030642.1 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:36122300 G>A maps to NM_030642.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:36690983 C>T maps to NM_002473.4 T1208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:37331725 C>T maps to ENST00000262825 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:39639935 G>A maps to NM_002608.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:40662284 C>G maps to ENST00000454349 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:40805699 G>A maps to NM_015705.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr22:46654092 C>G maps to NM_006071.1 L1709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:9055452 C>G maps to NM_014850.2 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:9803375 G>A maps to NM_003656.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:10127603 C>T maps to NM_033084.3 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:48447187 G>A maps to NM_001130082.1 L2082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:48626327 G>C maps to NM_000094.3 Y805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:48671064 C>T maps to NM_022911.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:49449865 G>T maps to NM_022171.2 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:51426366 G>A maps to ENST00000273628 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:56627023 C>T maps to NM_001141947.1 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:58106995 C>T maps to NM_001164317.1 F964F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:58377552 C>T maps to NM_017771.3 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:67054356 T>C maps to NM_032505.2 N322N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:71037149 G>A maps to NM_032682.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:93733303 T>C maps to NM_001001850.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:108102560 G>A maps to NM_014981.1 Q1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:113850097 C>T maps to NM_000796.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:120424962 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:121554152 C>T maps to NM_018456.4 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:122658316 C>T maps to NM_001031702.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:123699229 G>A maps to NM_017578.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:126676357 C>T maps to ENST00000508789 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:129293325 G>A maps to NM_015103.2 V846V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:138256168 C>T maps to NM_024491.2 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:138665348 C>T maps to NM_023067.3 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:139258347 C>T maps to NM_002899.3 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:141526644 G>A maps to NM_139209.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:141626054 C>T maps to NM_001679.2 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:152880886 T>C maps to NM_002886.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:154886392 G>A maps to NM_007289.2 W631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:182872116 G>A maps to NM_014398.3 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:186969424 C>T maps to NM_139125.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:193855628 C>T maps to NM_005524.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr3:197238891 G>A maps to NM_203315.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:887188 C>T maps to NM_005255.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:1746258 G>A maps to NM_006342.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:3344755 C>T maps to NM_198229.2 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:4303907 A>T maps to NM_145291.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:7044014 C>T maps to NM_153376.2 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:8237167 G>A maps to NM_018986.3 Q1097Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:22456498 G>A maps to NM_145290.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:25005687 G>C maps to NM_018176.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:39448202 C>T maps to NM_175737.3 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:39978092 C>T maps to NM_001100399.1 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:40103905 G>A maps to NM_018177.3 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:48605372 C>T maps to NM_015030.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:76434445 G>A maps to NM_015436.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:76895234 G>A maps to NM_018115.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:77660885 G>A maps to NM_020859.3 Q520Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:81123464 C>T maps to NM_001099403.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:87653920 T>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:100756842 C>T maps to NM_014395.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:110460767 G>C maps to NM_006323.2 R1248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr4:154525364 C>T maps to NM_001131007.1 F1067F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:475146 C>T maps to NM_004174.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:1081815 C>T maps to NM_006598.2 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:1081818 C>T maps to NM_006598.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:16680070 C>T maps to NM_012334.2 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:31302359 C>T maps to NM_004932.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:33641931 C>T maps to NM_030955.2 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:41009498 C>T maps to ENST00000296803 K1102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:52096665 C>T maps to NM_015946.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:64267617 G>A maps to NM_005869.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:109202633 C>T maps to NM_002372.2 Q1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:114879142 G>A maps to NM_020177.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:121758692 G>A maps to ENST00000379533 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:124036908 G>A maps to NM_020747.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:124080027 G>A maps to NM_020747.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:138661215 G>T maps to ENST00000394800 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:140308754 C>T maps to NM_018898.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:140431477 G>A maps to NM_013340.2 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:145252342 A>G maps to NM_001080516.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:150847395 C>A maps to NM_078483.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:159682611 C>T maps to NM_024565.5 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:167655044 G>A maps to NM_001122679.1 L1801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:169122854 C>T maps to NM_004946.2 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:170159844 G>A maps to NM_001034837.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:171517360 C>T maps to NM_005990.3 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:175816402 C>T maps to NM_138820.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:176309064 G>C maps to NM_002115.2 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:176721472 C>G maps to NM_022455.4 A2368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:178359070 C>T maps to NM_030613.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:178554963 G>A maps to NM_014244.4 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr5:179763569 C>T maps to NM_005110.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:7583090 C>T maps to NM_004415.2 Q1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:12123090 C>T maps to NM_002114.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:17804705 G>A maps to NM_022113.4 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:21065356 G>A maps to NM_017774.3 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:26217567 G>A maps to NM_021052.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:26368409 G>C did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:32977304 G>A maps to NM_002119.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:33245447 G>C maps to NM_003782.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:36452533 G>A maps to NM_173562.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:39895071 G>A maps to ENST00000425303 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:41121534 G>A maps to NM_178174.2 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:42532120 G>T maps to NM_015255.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:42713400 G>A maps to NM_003192.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:43190339 C>T maps to ENST00000354495 F2331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:43323778 C>T maps to NM_014345.2 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:46977463 G>A maps to ENST00000283297 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:49753658 G>A maps to NM_138733.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:51612669 G>A maps to NM_138694.3 F3248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:52103569 G>C maps to NM_052872.3 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:52129559 G>C maps to ENST00000419835 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:52701149 G>A maps to NM_153699.1 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:57183275 G>A maps to NM_000947.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:74150016 C>T maps to NM_138441.2 W343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:76425251 C>G maps to NM_015571.2 S1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:84618804 G>A maps to NM_016230.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:84862558 G>A maps to NM_014895.2 Q1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:97587082 C>T maps to NM_052904.3 F596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:126203597 G>A maps to NM_181782.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:129796543 A>C maps to NM_000426.3 A2483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:139094927 G>A maps to NM_015439.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:145160370 G>A maps to NM_007124.2 L3376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:148855933 C>G maps to NM_015278.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:155143462 C>T maps to NM_014892.3 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:159173047 C>T maps to ENST00000297239 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:159204663 G>A maps to NM_001111077.1 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:159677591 C>T maps to NM_032532.2 I1701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr6:168352585 C>T maps to ENST00000400822 L1510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:15601350 T>C maps to NM_001004320.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:16840962 G>A maps to ENST00000223274 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:18705861 G>A maps to NM_178425.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:36327381 G>A maps to NM_030636.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:42964296 C>T maps to NM_002787.4 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:51095843 C>T maps to ENST00000395542 Q1065Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:56141898 A>G maps to ENST00000395437 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:56142307 G>A maps to ENST00000395437 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:65554626 C>G maps to NM_000048.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:77539722 C>G maps to ENST00000427986 S258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:84702366 G>A maps to NM_152754.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:89854698 G>C maps to NM_152999.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:90894809 C>T maps to NM_003505.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:94540504 G>A maps to NM_001166160.1 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:97362007 G>A maps to NM_003182.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:98528284 C>T maps to ENST00000359863 I1141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:99021514 C>A maps to NM_001198879.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:99048376 C>T maps to NM_006693.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:100478980 C>T maps to NM_015908.5 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:100806759 G>A maps to NM_003378.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:128317716 C>A maps to NM_001012454.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:132990734 C>T maps to NM_021807.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:134873229 G>A maps to NM_014149.3 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:135329648 C>T maps to NM_015135.2 Q1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:136700169 C>G maps to NM_001006628.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:139083367 G>A maps to NM_016019.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:140301336 G>A maps to NM_015689.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:143747956 C>T maps to NM_012365.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr7:150814757 C>T maps to NM_031946.4 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:6914117 C>T maps to NM_021010.1 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:27361251 C>T maps to ENST00000458037 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:54965250 G>A maps to ENST00000419058 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:56015533 C>T maps to NM_052898.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:56015539 C>T maps to NM_052898.1 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:59555591 C>A maps to NM_001144772.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:66631544 G>A maps to ENST00000401827 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:67089334 G>A maps to NM_000756.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:67577465 G>A maps to NM_025054.4 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:100454825 G>A maps to NM_017890.3 E1136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:108509536 G>A maps to NM_001146.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:108509746 G>A maps to NM_001146.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:113518954 G>A maps to NM_198123.1 V1620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:117782535 G>C maps to NM_032334.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:124266209 C>A maps to NM_007222.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:144898722 C>T maps to NM_078480.1 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:144940698 C>T maps to NM_031308.1 E2241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:145151086 C>T maps to NM_001916.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr8:145583547 C>T maps to NM_024531.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:2060920 C>T maps to NM_003070.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:4661988 G>A maps to ENST00000454239 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:6007316 G>A maps to NM_001017969.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:6605253 C>T maps to NM_000170.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:7799695 G>A maps to NM_033428.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:33264453 C>T maps to NM_004323.5 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:35732997 G>A maps to NM_006368.4 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:75567868 C>T maps to NM_000689.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:92220695 C>T maps to NM_006705.3 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:95482794 G>C maps to NM_001003800.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:96714548 G>C maps to NM_021570.3 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:101767277 C>A maps to NM_001855.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:101980575 C>T maps to NM_033087.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:117359914 C>T maps to NM_004888.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:123924224 G>A maps to NM_007018.4 E1727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130027209 G>A maps to NM_032293.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130083017 G>A maps to NM_032293.4 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130592028 G>A maps to NM_001114753.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:130981397 C>T maps to ENST00000372923 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:131019546 C>T maps to NM_004486.4 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:131843463 C>T maps to NM_020438.4 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:133799255 G>A maps to NM_001145106.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:138662867 G>A maps to ENST00000298480 K645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:138713632 G>A maps to ENST00000409386 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:139907258 C>T maps to ENST00000355090 Q1692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:140083656 G>A maps to NM_003731.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chr9:140446922 C>T maps to NM_032477.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:12906157 C>A maps to NM_016562.3 S844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:15809080 G>A maps to NM_005089.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:48890999 G>C maps to ENST00000336239 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:49079297 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:57935504 G>A maps to NM_007156.4 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:71494971 C>T maps to NM_001007.4 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:71846899 C>G did not map to a codon.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:73812834 G>A maps to NM_183353.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:132162128 C>T maps to NM_031907.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:152137986 C>T maps to NM_001178106.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AC-01A-11D-A13W-08 chrX:153580261 G>C maps to NM_001110556.1 V2299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:22176611 C>G maps to NM_005529.5 L2456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:23382466 C>G maps to NM_001009999.2 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:24392392 G>A maps to ENST00000330966 L1177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:27058056 C>T maps to NM_006015.4 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:90400468 A>G maps to NM_001134479.1 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:94343391 C>T maps to NM_014597.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:117699367 C>A maps to NM_024626.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:144918838 C>T maps to NM_014644.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:151205034 C>T maps to NM_001135638.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:151205058 C>T maps to NM_001135638.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr1:179019500 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr10:75184442 G>C maps to NM_001024593.1 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr10:105361656 A>G maps to ENST00000369774 N1106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:8947286 C>T maps to NM_020643.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:10022531 C>A maps to NM_030962.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:17538983 A>G maps to NM_005709.3 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:55371621 G>T maps to NM_001004700.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr11:128807620 G>A maps to NM_022112.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:14927571 G>A maps to NM_177925.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:30829449 G>A maps to NM_006390.3 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:51090910 C>A maps to NM_173602.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:72388269 G>A maps to ENST00000389376 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr12:123471234 C>T maps to NM_020845.2 P1185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr13:30829723 G>A maps to NM_032116.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr13:32929378 T>C maps to NM_000059.3 N2463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr13:61057915 C>G maps to NM_001146070.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr14:96757943 G>A maps to NM_018036.5 R1858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr15:69746005 C>T maps to NM_001003.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr16:3786147 A>C maps to NM_004380.2 Y1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr16:31141846 C>T maps to NM_182958.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr16:66881068 C>T maps to NM_005182.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:1003884 G>A maps to NM_021962.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:1003906 G>A maps to NM_021962.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:19480736 G>A maps to ENST00000395585 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:48681581 C>A maps to NM_018896.3 I1412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr17:48681611 C>T maps to NM_018896.3 F1422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr18:46904946 A>G maps to NM_017653.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:8193910 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:12059540 C>T maps to NM_144566.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:36369851 C>T maps to NM_001024807.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:44099433 C>T maps to NM_001007561.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr19:45375389 G>A maps to NM_001042724.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:42284439 C>T maps to NM_138370.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:211158489 C>T maps to NM_079420.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:211525294 G>A maps to NM_001122633.1 K1287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:212522498 G>A maps to NM_005235.2 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr2:232156133 C>T maps to ENST00000359743 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr20:76883 G>C maps to NM_153325.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr20:17446012 C>G maps to NM_002594.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr20:62340258 G>A maps to NM_032527.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr21:31964949 C>T maps to ENST00000399871 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr3:42678912 C>T maps to NM_005385.3 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr3:145806414 C>T maps to NM_182943.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr3:169706097 C>T maps to NM_003262.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr4:122590870 C>T maps to NM_001154.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr4:126411828 G>T maps to NM_024582.4 E4618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:33964005 G>A maps to NM_016180.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:53839069 G>A maps to NM_001102575.1 Q561Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:72419556 C>T maps to NM_173490.6 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:114466548 A>G maps to NM_018700.3 N524N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A1AD-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr5:140559900 G>A maps to NM_019120.2 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:18212789 G>A maps to ENST00000388870 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:27834977 G>C maps to NM_005322.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:144508324 C>T maps to NM_003764.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr6:144820448 G>A maps to NM_007124.2 K1550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:57528874 T>C maps to NM_001159279.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:99753311 C>G maps to NM_018275.3 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:127670602 G>A maps to NM_022143.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:128355644 G>T maps to NM_032599.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr7:155093958 A>C did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:36662754 T>C maps to NM_001031836.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:61653989 A>T did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:110100397 C>T maps to NM_003301.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:119122780 G>A maps to NM_000127.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:124267127 C>T maps to NM_007222.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:126061283 G>A maps to ENST00000377985 N786N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr8:144895028 G>A maps to NM_182706.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:26984495 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:35044992 C>G maps to NM_203299.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:35697853 C>T maps to NM_006289.3 K2520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:71844145 T>G maps to NM_004817.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:78784731 C>T maps to NM_001190482.1 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:95477534 G>A maps to NM_001003800.1 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chr9:98221996 C>A maps to NM_000264.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chrX:34150088 G>A maps to NM_203408.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chrX:35959431 C>G maps to NM_152632.3 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AD-01A-11D-A13W-08 chrX:123190028 G>T maps to NM_001042750.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:9164615 G>C maps to NM_024980.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:13475072 C>T maps to NM_001099850.1 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr1:196434451 T>A maps to NM_198503.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr10:29752433 G>C maps to NM_021738.2 L2088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr10:99527600 G>T maps to NM_003015.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr11:3249612 C>T maps to ENST00000328215 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr11:65046237 C>T maps to NM_002689.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr11:117164661 G>C maps to NM_012104.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:48866716 C>T maps to NM_012404.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:49427905 C>A maps to NM_003482.3 E3562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr12:79611343 C>A maps to NM_005639.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr14:75745826 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr15:73624588 G>T maps to NM_005477.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr15:75248519 G>A maps to NM_017793.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr15:100673516 G>A maps to NM_139057.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr16:4411440 C>T maps to NM_024535.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr16:89261394 G>A maps to NM_004933.2 E759E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr17:38178226 G>T maps to NM_014815.3 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr17:73235615 G>A maps to NM_138619.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr17:78079574 G>T maps to NM_001079804.1 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:4523683 C>T maps to NM_001013706.2 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:42752673 C>A maps to NM_006494.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:50978630 A>G maps to ENST00000391816 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr19:54677812 A>C maps to NM_024298.3 G448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:27898483 G>A maps to NM_018158.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:179413247 C>T maps to NM_133378.4 L28467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:219360634 C>A maps to NM_020935.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr2:219503171 G>A maps to NM_001105537.1 Q1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr22:17600372 G>A maps to NM_031890.3 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr3:38739748 G>A maps to NM_006514.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr4:155530853 C>T maps to ENST00000407946 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr6:36067963 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr6:44081612 G>A maps to NM_032111.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr6:90428325 C>T maps to NM_014611.1 W2114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr7:99722456 A>G maps to NM_152755.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr8:103851003 C>T maps to NM_148174.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr8:146108081 C>G maps to NM_021061.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chr9:115600916 C>T maps to NM_001012994.1 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AE-01A-11D-A13W-08 chrX:66765005 G>A maps to NM_000044.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr1:156507073 G>A maps to NM_178229.4 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr1:205819092 C>T maps to NM_152491.4 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr11:33053079 G>A maps to NM_001077242.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr11:34139780 C>G maps to NM_024662.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr11:74056621 C>T maps to NM_173582.3 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:10780302 A>C maps to NM_018423.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:53662887 G>A maps to NM_012291.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:54894396 C>T maps to NM_005337.4 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:64588248 C>T maps to ENST00000311915 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr12:124362398 C>T maps to NM_207437.3 F2654F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr13:96409942 C>T maps to NM_006260.4 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr14:45658432 G>C maps to NM_020937.2 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr14:50118049 T>C maps to NM_002692.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr15:49076284 C>T maps to NM_001194998.1 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr16:75669619 G>T maps to NM_001130089.1 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr17:8168265 G>A maps to NM_012393.2 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr17:45913411 G>A maps to NM_033413.3 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr17:79660898 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr18:29617077 G>T did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr19:21720335 C>G maps to NM_001001415.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr2:64208890 G>A maps to NM_016516.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr2:111427075 G>C maps to NM_004336.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr2:135739073 G>A maps to NM_025052.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr20:61391507 C>G maps to NM_002531.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr22:39141784 C>T maps to ENST00000405018 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr22:42209813 C>T maps to NM_024821.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:110845148 C>T maps to NM_015480.1 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:124646826 T>C maps to NM_033049.3 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:125726026 C>T maps to NM_001008485.1 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:186383943 C>T maps to NM_000412.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr3:195593872 G>A maps to NM_001010938.1 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr4:55961743 C>T maps to NM_002253.2 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr4:79294004 C>G maps to NM_025074.6 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr4:148743973 G>A did not map to a codon.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr6:28333832 G>A maps to NM_024493.2 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr6:35088707 C>T maps to NM_001093728.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr7:4794947 G>C maps to ENST00000450194 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr7:100410819 G>A maps to NM_004444.4 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr7:155094080 C>T maps to ENST00000344756 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chr8:104898275 C>G maps to NM_001100117.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chrX:1508488 G>A maps to NM_001636.3 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chrX:55514286 C>G maps to NM_201286.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AF-01A-11D-A13W-08 chrX:123179196 C>T maps to NM_001042750.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr1:24419479 C>T maps to ENST00000330966 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr1:205240949 G>T maps to NM_014858.3 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr10:24810778 C>T maps to NM_019590.3 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr11:94599319 G>A maps to NM_130847.2 W825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr11:102709925 C>T maps to NM_002422.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr12:32873664 C>T maps to ENST00000381000 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr13:52952894 G>A maps to NM_018676.3 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr14:21894344 G>C maps to NM_001170629.1 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr14:50472403 C>T maps to NM_001012706.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr15:45399060 G>A maps to NM_014080.4 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr15:75248615 G>C maps to NM_017793.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:723542 C>T maps to NM_138769.1 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:2012570 C>T maps to NM_002952.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:3021897 C>T maps to NM_152341.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:26146938 G>A maps to NM_006040.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr16:58320014 G>A maps to NM_001080492.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr17:35343959 C>T maps to NM_012138.3 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr17:38457717 A>G did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr17:78318807 C>T maps to NM_020914.4 Q2274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr18:33077829 C>T maps to NM_001098817.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:2213963 C>A maps to ENST00000221482 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:2222506 C>T maps to ENST00000221482 V1113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:3747940 C>T maps to NM_014428.1 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:6007098 C>T maps to NM_000635.3 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:16532170 G>A maps to ENST00000455140 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:49119426 G>A maps to NM_000979.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:54403678 C>T maps to NM_002739.3 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:55773976 C>G maps to NM_012267.4 *360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:56969550 C>A maps to ENST00000342634 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr19:57910374 C>T maps to NM_001172773.1 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:27301965 C>G maps to NM_007046.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:118731528 G>C maps to NM_019044.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:136519443 C>T maps to NM_014607.3 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:163029726 G>C maps to NM_004460.2 S680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr2:170917626 G>A maps to ENST00000442603 L1637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr21:37833618 G>A maps to NM_001146077.1 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr21:45681065 G>C maps to NM_013369.2 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr22:44364694 C>T maps to NM_015380.4 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:3516517 G>A maps to NM_002337.2 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:110866375 G>A maps to NM_001963.4 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:119736284 G>A maps to ENST00000379735 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr4:141578844 T>C maps to NM_015130.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr5:140249092 C>G maps to NM_018902.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr5:156946864 G>T maps to ENST00000430702 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr5:167986162 C>T did not map to a codon.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr6:10621626 C>T maps to NM_145649.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr6:70098734 G>C maps to NM_001704.2 L1507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr7:24911607 C>T maps to NM_015550.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr7:65553884 C>T maps to NM_000048.3 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr8:134042189 C>T maps to NM_003235.4 G2387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr8:144803971 G>A maps to NM_139021.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chr9:40773178 G>C maps to NM_033160.5 S699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A1AG-01A-11D-A13W-08 chrX:70621445 A>G maps to ENST00000449580 Q1284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:15870966 C>T maps to NM_015291.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:27099360 C>T maps to NM_006015.4 Q1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:158596662 G>A maps to NM_003126.2 F1933F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:182841624 C>T maps to NM_001357.4 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:197890577 C>T maps to NM_020204.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:228589811 C>T maps to NM_145214.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:237729961 G>T maps to NM_001035.2 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr1:249142537 C>T maps to NM_024836.1 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr10:104491932 C>T maps to NM_178858.4 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr10:106075628 G>T maps to NM_033397.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr11:64875071 G>A maps to NM_013265.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr11:66241240 C>T maps to NM_145065.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr12:100731226 G>A maps to NM_017988.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr14:60619881 G>A maps to NM_016029.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr14:93125803 C>T maps to NM_024832.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr15:63984689 G>C maps to ENST00000261887 S1917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr15:65983667 G>A maps to ENST00000443035 L1088L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr18:44555114 G>A maps to NM_145653.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr18:59166705 C>T maps to NM_031891.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr19:18499743 G>C maps to NM_004864.2 *309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr19:19613327 C>A maps to ENST00000404158 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr19:56466504 G>T maps to NM_176811.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr2:27439744 C>T maps to NM_080592.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr21:47423836 C>T maps to NM_001848.2 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr3:8590589 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr3:64589990 G>T maps to NM_182920.1 S1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr3:160137214 C>T maps to NM_005496.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:4190622 G>A maps to NM_177998.1 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:47584074 G>A maps to NM_020453.3 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:151729480 G>C maps to NM_006726.3 S1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr4:152086848 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr5:33937954 G>A maps to NM_016568.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr5:66459602 G>A maps to NM_001164664.1 L1532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr5:139914967 C>G maps to ENST00000253810 S2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr6:10410337 C>T maps to ENST00000379613 Q94Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr6:132966335 G>T maps to NM_138327.1 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:2259076 C>T maps to NM_003550.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:141490166 G>A maps to NM_018980.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:142605799 C>T maps to NM_019841.4 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr7:150417943 C>T maps to NM_130759.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr8:11996071 C>T maps to NM_201402.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr8:106573709 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr9:14746433 C>T maps to ENST00000380880 W2060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chr9:131243908 G>A maps to NM_153435.1 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chrX:1553954 G>A maps to NM_004192.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2HX-01A-12D-A18F-08 chrX:32235110 T>C maps to ENST00000357033 L2120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:6704688 C>T maps to NM_018198.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:11854537 C>G maps to ENST00000376585 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:43228146 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:47728682 C>A maps to NM_001048166.1 G907G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:111853045 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:149906157 C>T maps to NM_001145862.1 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:155931989 G>A maps to NM_001162383.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:156565922 A>G maps to NM_015590.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr1:206623768 C>G maps to ENST00000414359 S636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr10:46967614 C>T maps to NM_031912.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr10:115534018 G>T maps to NM_182601.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr10:116602894 C>T maps to NM_020940.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:59828719 G>C maps to NM_006138.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:63320519 C>T maps to NM_017878.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:64032896 C>T maps to NM_000932.2 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:66134018 G>T maps to NM_001532.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:67059206 C>T maps to NM_207354.2 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:77919931 C>G maps to NM_020798.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:111941993 G>A maps to NM_138789.3 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr11:118023347 C>T maps to NM_174934.3 W14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:51467661 G>A maps to NM_030809.1 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:57397507 G>A maps to NM_014830.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:105151418 G>A maps to NM_018413.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr12:124968283 G>C maps to NM_006312.4 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr13:28239828 G>A maps to NM_152705.1 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:23884263 G>A maps to NM_000257.2 N1833N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:32562187 G>A maps to NM_001030055.1 K771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:36219783 G>A maps to NM_194301.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr14:47120420 G>A maps to NM_080746.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr15:55790517 G>A maps to NM_130810.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr15:55790546 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr15:90169197 G>C maps to NM_152259.3 R1836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr16:58572153 G>A maps to NM_016284.3 R1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr16:82131776 C>T maps to NM_002153.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:8396108 C>T maps to ENST00000360416 Q1481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:26646321 C>T maps to NM_014573.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:26691930 G>A maps to NM_001080837.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:37627780 C>T maps to NM_016507.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:42828542 C>T maps to NM_145663.2 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:42850283 C>T maps to NM_002390.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:42942370 C>T maps to NM_004247.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr17:62496162 G>A maps to NM_004396.3 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr18:67992476 G>A maps to NM_004232.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:4333711 C>A maps to ENST00000314714 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:5784137 G>C maps to CCDS12150.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:12738663 A>G maps to NM_153358.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:13919936 C>G maps to NM_023072.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:15587201 C>G maps to NM_052890.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:15587363 C>T maps to NM_052890.3 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:41944169 C>T maps to ENST00000417807 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:45296768 G>A maps to NM_012116.3 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr19:53209075 G>C maps to NM_001161500.1 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:114399704 G>A maps to ENST00000409875 *239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:121043652 A>G maps to NM_002881.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:133543045 G>C maps to NM_207363.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:157406240 G>A maps to NM_000408.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:219029262 G>A maps to NM_000634.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr2:231947595 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr20:2640191 C>T maps to NM_006899.2 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr20:5282739 G>C maps to NM_144773.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr20:32255545 G>A maps to NM_001024675.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr21:45104495 C>T maps to NM_015056.2 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:31859019 G>A maps to NM_019843.3 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:38061587 G>T maps to ENST00000442465 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:39218742 G>A maps to NM_014293.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr22:41077226 C>T maps to NM_005297.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:440698 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:9424927 C>T maps to NM_015453.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:9877037 C>T maps to NM_001025930.3 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:11880709 G>A maps to ENST00000444133 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:31921291 G>A maps to NM_017784.4 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:48510921 G>A maps to NM_016479.3 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:120315334 G>A maps to NM_004547.5 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:142122728 C>T maps to NM_019001.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr3:158386886 G>A maps to NM_020169.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:845580 C>T maps to NM_005255.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:2916621 G>C maps to NM_014189.2 V570V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:86915952 C>A maps to NM_001025616.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:104070086 C>A maps to NM_001813.2 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr4:160264206 C>T maps to NM_014247.2 Q838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:13913929 G>A maps to NM_001369.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:55094376 C>G maps to NM_024415.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:88100567 C>T maps to NM_002397.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr5:94876438 G>A maps to NM_014639.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr6:87970066 C>T maps to NM_015021.1 D2240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr6:133072622 C>G maps to NM_004665.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:6865861 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:66270178 C>T maps to ENST00000451741 I508I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-A2I1-01A-11D-A17V-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr7:102988223 C>T maps to NM_002803.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr8:22398213 C>A maps to ENST00000397775 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr8:122626945 C>T maps to NM_005328.2 W354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr8:144994321 C>A maps to NM_201380.2 E3360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr9:72047529 G>A maps to NM_001163.3 I788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr9:85677429 G>T maps to NM_152573.2 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chr9:137591827 C>T maps to NM_000093.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chrX:12937403 C>G maps to ENST00000311912 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chrX:70148784 C>T maps to NM_032803.5 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chrX:129208116 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chrX:137939731 G>A maps to NM_001139500.1 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I1-01A-11D-A17V-08 chrX:153206996 G>A maps to NM_002910.5 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:29379625 C>A maps to NM_001166005.1 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:89729592 C>T maps to NM_052942.3 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:112998770 A>G maps to NM_018704.2 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:144859923 G>A maps to NM_014644.4 L2054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:153921066 A>G maps to NM_181715.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:155721968 C>T maps to ENST00000368331 V2085V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:209799288 G>C maps to NM_000228.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:217915424 C>T maps to NM_138796.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:227316870 G>A maps to ENST00000366766 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:242253335 C>T maps to NM_152666.2 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr1:248344189 C>T maps to NM_001004688.1 F301F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr11:44135764 G>C maps to NM_000401.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr11:65308026 G>A maps to NM_001130144.2 N1012N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr11:93796803 G>C maps to NM_001098672.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr12:9020632 C>T maps to NM_144670.3 Q1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr12:26818877 G>A maps to NM_002223.2 Q506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr13:70681398 G>A maps to NM_020866.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr15:54586191 T>C maps to ENST00000260323 D1306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr16:19058552 C>T maps to NM_024847.3 I574I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr17:10248879 C>A maps to NM_003802.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr17:38244571 C>T maps to NM_003250.5 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr17:62254696 G>T maps to NM_018469.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr19:42383360 T>G did not map to a codon.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr2:97530100 C>T maps to NM_017789.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr20:50224072 G>A maps to NM_006045.1 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr21:42823169 G>A maps to NM_001144925.1 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:36872484 T>C maps to NM_014831.2 V2819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:138478131 C>T maps to NM_006219.1 W18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr3:155571495 G>A maps to NM_004733.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:1643301 G>A maps to NM_001174070.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:2831313 C>T maps to NM_001145856.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:153244123 G>C maps to NM_033632.2 S678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr4:173269793 G>A maps to NM_001034845.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr5:137727501 G>A maps to NM_016604.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:4117577 C>T maps to NM_206836.2 W331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:36168332 G>A maps to NM_015695.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:54095690 C>T maps to ENST00000502396 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr6:144508444 C>G maps to NM_003764.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr7:87473128 T>C maps to NM_018843.3 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr7:95041044 A>G maps to NM_000305.2 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr7:98639809 G>A maps to NM_020429.2 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr8:10755761 C>T maps to NM_173683.3 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr8:110592171 G>T maps to NM_001099744.1 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr8:120577109 G>A maps to NM_006209.3 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chr9:130496822 G>A maps to NM_001085347.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chrX:44949017 G>A maps to NM_021140.2 W1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chrX:130411012 G>T maps to NM_001170961.1 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I2-01A-11D-A17V-08 chrX:153609240 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:3662531 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:12061570 C>G maps to NM_014874.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:12322039 G>A maps to NM_015378.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:14925612 G>C maps to NM_201628.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:15986461 C>G maps to NM_006511.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:15987252 C>A maps to NM_006511.1 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:20944967 C>T maps to NM_001785.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:24078044 C>G maps to NM_003198.2 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:27216179 G>A maps to NM_018066.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:27950378 C>A maps to NM_005248.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:28365385 G>T maps to NM_001990.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:29030719 C>T maps to NM_006582.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:33613175 C>A maps to NM_018207.2 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:38041279 C>T maps to NM_013285.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:38511338 G>C maps to NM_002699.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:39876716 G>A maps to NM_015038.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:40945003 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:48918749 G>A maps to NM_019073.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:78444568 C>T maps to ENST00000436586 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:85498381 C>T maps to NM_018298.9 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:101004981 C>T maps to NM_022049.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:101705412 C>T maps to NM_001400.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:110555026 G>A maps to NM_006621.4 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:113058963 C>T maps to NM_024494.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:113464732 C>T maps to NM_003051.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:120438389 C>T maps to NM_021794.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:145682085 T>C maps to NM_014455.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:148009409 G>A maps to ENST00000310701 Q638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152193079 G>C maps to NM_001009931.1 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152944473 G>A maps to NM_173080.1 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:152944533 G>A maps to NM_173080.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:155292223 C>T maps to NM_001105203.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:155631205 C>T maps to ENST00000368339 K434K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156438786 G>A maps to NM_005920.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156594396 G>A maps to NM_021817.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156642911 G>T maps to NM_006617.1 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:156815421 G>A maps to NM_014215.2 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:160389331 C>T maps to NM_020335.2 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:161276524 G>A maps to ENST00000360451 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:161993193 G>A maps to ENST00000451379 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:162535884 G>A maps to ENST00000367925 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:167367229 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:167653185 C>A maps to NM_052862.3 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:167849780 G>A maps to NM_018417.4 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:169446800 G>A maps to NM_006996.2 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:175097776 G>A maps to NM_022093.1 Q1075Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:179054979 C>T maps to NM_022371.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:179600038 G>A maps to ENST00000444136 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:179883174 C>G maps to ENST00000398836 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:186037085 G>A maps to NM_031935.2 W2609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:186322837 C>T maps to NM_003292.2 E772E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:206821904 G>A maps to NM_003582.2 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:209968638 G>A maps to NM_006147.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:215916587 G>A maps to ENST00000366943 Q3827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:226567865 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:228466438 G>A maps to NM_001098623.1 E2303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:235292006 G>A maps to NM_014765.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:235920622 G>A maps to NM_000081.2 L2339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr1:244868943 G>A maps to NM_016076.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:5810188 G>C maps to NM_001494.3 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:17276804 C>T maps to NM_003380.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:21804707 G>A maps to NM_207371.3 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:30317489 C>G maps to NM_020848.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:34420502 G>C maps to NM_019619.3 S1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:78708986 G>C maps to NM_001161352.1 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:99416091 G>A maps to ENST00000416867 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:100174796 C>T maps to NM_032709.2 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:104678578 G>A maps to NM_017649.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:105179395 G>A maps to NM_014976.1 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr10:105207265 G>C maps to NM_015916.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:209945 C>T maps to NM_021932.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:1272546 C>T maps to ENST00000447027 L4816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:10823910 G>A maps to ENST00000429377 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:14280907 G>A maps to NM_006108.2 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:18057566 C>T maps to ENST00000341556 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:46917827 C>T maps to ENST00000256991 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:47660528 G>C maps to NM_014342.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:61545870 G>A maps to NM_001127392.1 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:61545876 G>A maps to NM_001127392.1 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:62570908 C>T maps to NM_006362.4 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:62575049 G>C maps to NM_003164.3 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:63486764 C>G maps to ENST00000377819 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:64082559 C>G maps to NM_004451.3 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:64694349 C>T maps to NM_006244.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:68748224 G>A maps to NM_198923.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:71725722 C>T maps to ENST00000393695 A948A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:71932541 C>T maps to NM_001113536.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:74419416 G>C maps to NM_015424.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:74651850 G>A maps to NM_182969.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:82879594 C>T maps to NM_015885.3 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:83195223 G>A maps to NM_001142699.1 F747F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:93912932 C>T maps to NM_015368.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:94533393 C>G maps to NM_130847.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:104821780 G>A maps to NM_001225.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr11:124623757 G>A maps to NM_138961.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:2017149 G>A maps to NM_172364.4 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:7527245 C>G maps to ENST00000416109 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:10149468 C>A maps to NM_016509.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:19593294 C>A maps to NM_001114176.1 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:26589262 G>A maps to NM_002223.2 F2220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:49934724 C>T maps to NM_012284.1 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:49935416 C>A maps to NM_012284.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:50616147 C>A maps to NM_001113546.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:53607027 C>T did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:56816719 G>C maps to NM_003920.3 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:56817141 G>C maps to NM_003920.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:56827389 G>A maps to NM_003920.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:57586682 C>T maps to NM_002332.2 L2495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:81472104 C>A maps to NM_024560.2 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:111957799 G>C maps to NM_002973.3 S450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:120118102 C>T maps to NM_006253.4 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:123253410 C>T maps to ENST00000455982 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:131471688 G>A maps to NM_198827.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr12:133327435 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:25067845 G>C maps to NM_006437.3 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:28141890 G>A maps to NM_153371.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:32709060 C>T maps to NM_023037.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:33017212 C>T maps to NM_033111.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:33700223 G>C maps to NM_178007.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:39433624 C>T maps to NM_207361.4 Q2473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:41767322 G>C maps to NM_032138.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:46942257 G>A maps to NM_025113.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:47263285 G>C maps to NM_001164211.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr13:88328434 T>A maps to NM_015567.1 C264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:20444468 G>A maps to NM_001005486.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:24768167 G>A maps to NM_001136050.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:59965516 G>A maps to ENST00000356057 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:68159245 C>T maps to NM_016026.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:76211451 C>G maps to NM_015072.4 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:92588064 C>T maps to NM_004545.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:94088397 C>T maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:94128991 C>T maps to ENST00000393153 Q2251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:102552648 G>A maps to NM_001017963.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:104121116 C>T maps to ENST00000445352 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr14:105354097 G>A maps to ENST00000453495 R1175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:42691774 C>T maps to NM_000070.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:59358968 C>G maps to ENST00000434298 S458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:89449883 G>A maps to NM_005928.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr15:101566279 C>G maps to NM_024652.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:676020 C>T maps to NM_021168.4 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:1536455 G>A maps to NM_001013658.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:1575299 G>A maps to NM_014714.3 F932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:2812175 G>A maps to NM_016333.3 Q549Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:2812361 G>C maps to NM_016333.3 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:2835104 G>A maps to NM_152891.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:3191254 C>T maps to NM_001134655.1 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4310138 G>A maps to NM_003223.2 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4934818 C>T maps to NM_002705.4 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4934920 C>T maps to NM_002705.4 E1245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:4935358 C>T maps to NM_002705.4 K1099K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:20999080 G>C maps to NM_017539.1 V2272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:25232863 C>G maps to NM_001169.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:31049269 C>T maps to NM_004604.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:31499001 C>T maps to ENST00000431354 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:48177915 G>A maps to NM_033226.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:50745518 C>G maps to NM_022162.1 S566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:67233111 G>A maps to NM_024712.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:70551627 C>T maps to NM_015386.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr16:88690428 C>T maps to ENST00000452588 I643I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:3337108 G>A maps to NM_003554.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:3593965 G>A maps to ENST00000435558 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:6719157 C>T maps to NM_053285.1 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:7758848 C>T maps to NM_203411.1 L99L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A2I4-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DK-A2I4-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:15902869 C>G maps to NM_017775.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:17700428 G>A maps to ENST00000395776 Q1389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:19316426 C>T maps to NM_007148.4 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:26964033 G>A maps to NM_014680.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:27186106 G>A maps to NM_005702.2 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:27419971 C>T maps to NM_078471.3 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:29490349 C>T maps to NM_001042492.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:29848999 C>T maps to NM_032932.3 Q276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:33288629 G>C maps to NM_052857.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:35627677 G>A maps to NM_198834.1 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37809999 G>C maps to NM_006804.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37884047 C>G maps to NM_004448.2 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37884179 C>T maps to NM_004448.2 F1217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:37947693 G>A maps to NM_012481.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:40169362 C>T maps to NM_003315.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:42850645 C>G maps to NM_002390.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:47109290 G>A maps to NM_006546.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:47886482 G>A maps to NM_007067.4 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:48155408 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:48218656 G>C maps to NM_032595.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:61767078 G>A maps to NM_203351.1 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:64880759 C>T maps to NM_014404.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:71348645 G>A maps to NM_001144952.1 F1908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:72846449 G>C maps to NM_000835.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:73663484 C>G maps to NM_013260.6 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:73753569 G>C maps to NM_001005619.1 V1784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:74005808 G>A maps to NM_001988.2 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:76047218 G>A maps to NM_001142640.1 W692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:76113905 G>C maps to NM_007267.6 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:78971125 G>A maps to NM_024591.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:79479014 C>A maps to NM_001614.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:79817198 C>T maps to NM_000918.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr17:80616442 G>A maps to NM_006822.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:3131436 G>C maps to NM_003803.3 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:30926329 G>T maps to NM_001105528.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:44555294 C>A maps to NM_145653.3 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:55273931 C>G maps to NM_004539.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:70205476 C>T maps to NM_182511.3 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr18:74962761 C>G maps to NM_001480.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:746780 G>A maps to NM_002579.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:814709 G>A maps to NM_024888.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:1123978 G>A maps to NM_014963.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:1461972 G>A maps to NM_005883.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:1462068 G>T maps to NM_005883.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:2222185 C>G maps to ENST00000221482 L1006L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:2876262 G>A maps to NM_024967.1 E101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:3017852 C>T maps to NM_003260.4 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:4446588 G>C maps to NM_025241.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:4538476 C>T maps to NM_052972.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:7166276 G>C maps to NM_000208.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:7960595 C>G maps to NM_025061.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:8175798 G>A maps to NM_032447.3 N1421N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:8661944 C>T maps to NM_030957.2 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:9091499 C>T maps to NM_024690.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:9873967 G>A maps to NM_001077624.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:9967497 G>A maps to NM_058164.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:11286643 G>A maps to NM_015493.6 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:12639429 G>C maps to NM_144976.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:12739579 G>T maps to NM_153358.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:12969527 C>T maps to NM_014975.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:13054367 C>T maps to NM_004343.3 I326I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:18507659 G>A maps to NM_145256.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:18632760 C>T maps to NM_006532.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:18684187 C>G maps to NM_003333.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:19033502 C>T maps to NM_019070.4 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:33135287 G>A maps to NM_032139.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:35449695 G>A maps to NM_175872.4 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:36219889 C>T maps to NM_014727.1 F1564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:38860797 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:39114741 C>T maps to NM_013234.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:42509941 G>A maps to NM_002088.3 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:42798382 C>A maps to NM_015125.3 S1418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:45287646 G>A maps to NM_012116.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:46094947 G>A maps to NM_005282.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:46174546 C>T maps to NM_000164.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:49840235 C>T maps to NM_001774.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:54942275 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:55453051 G>A maps to ENST00000446217 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:56688512 C>T maps to NM_033106.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr19:58117276 G>A maps to NM_020880.3 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:16085690 C>T maps to NM_005378.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:31598299 G>A maps to NM_000379.3 F516F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:32640518 G>A maps to NM_016252.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:44102358 G>A maps to NM_022437.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:54843420 G>A maps to NM_003128.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:62450305 G>C maps to NM_006577.5 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:70485406 C>T maps to NM_016297.3 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:96780655 G>A maps to NM_000682.5 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:96932159 G>A maps to NM_004804.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:101554279 C>T maps to NM_002518.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:113417183 C>G maps to NM_005415.3 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:113593148 C>T maps to NM_000576.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:119600618 G>A maps to NM_001426.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:131520310 C>G maps to NM_001105195.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:141093287 C>T maps to NM_018557.2 L4004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:160667044 G>C maps to NM_001198759.1 S1564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:160869837 G>A maps to NM_007366.4 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:176958256 C>T maps to NM_000523.3 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:177016456 G>A maps to NM_014621.2 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:179489390 C>T maps to NM_133378.4 L12304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:217300155 C>T maps to NM_014140.3 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:233243988 G>A maps to NM_001632.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr2:241398600 C>T maps to NM_002081.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:20621417 G>A maps to NM_020343.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:31661409 G>A maps to NM_182658.1 *477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:33875385 G>C maps to NM_178468.4 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:40079710 C>T maps to NM_032221.3 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:43113070 G>A maps to NM_024331.3 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:43132466 G>A maps to NM_006811.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:45012096 C>T maps to ENST00000439931 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:48562720 G>A maps to NM_018683.3 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:50051745 G>A maps to NM_012340.3 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:55033554 C>T maps to NM_020356.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:60768598 C>T maps to NM_015666.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:61300306 C>T maps to NM_016354.3 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr20:62421336 C>T maps to NM_025224.2 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:38126564 G>A maps to NM_000411.5 I721I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:38461128 G>A maps to NM_003316.3 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:43704786 C>T maps to NM_004915.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:44329052 C>G maps to NM_021075.3 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr21:46321535 G>A maps to NM_000211.3 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:21272302 G>A maps to NM_005207.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:22330075 C>T maps to NM_003935.3 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:24579486 C>A maps to NM_019601.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:29737584 G>A maps to NM_001127.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:30730591 C>T maps to NM_005877.4 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:31019014 C>T maps to NM_000355.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36587671 C>T maps to ENST00000332987 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36623579 G>C maps to ENST00000451256 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:36698619 G>A maps to NM_002473.4 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:39387536 C>T maps to ENST00000402182 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:42606364 G>A maps to NM_005650.1 I1649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:50921130 C>T maps to NM_024866.4 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr22:51017893 G>T maps to NM_005198.4 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:11404345 G>A maps to NM_006395.2 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:13401904 G>A maps to NM_024923.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:47958224 T>C maps to ENST00000426837 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:50331092 G>C maps to NM_003549.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:52557549 C>T maps to NM_015136.2 I2416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:53844149 C>G maps to NM_001128840.1 S2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:120128497 G>A maps to NM_007085.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:122459617 C>T maps to NM_024610.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:123014972 C>T maps to NM_183357.2 Q1007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:124211636 G>A maps to NM_001024660.3 V1578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:124456778 C>G maps to NM_000373.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:124456863 C>T maps to NM_000373.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:128991686 C>G maps to NM_016128.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:132215490 C>T maps to NM_015268.3 F1380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:136574264 C>G maps to NM_025246.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:137790533 C>T maps to NM_173543.2 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:138724387 C>T maps to NM_001134659.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:150903166 G>T maps to NM_053002.4 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:151155889 G>A maps to NM_178822.4 I2153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:151166755 G>C maps to NM_178822.4 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr3:191100572 G>A maps to NM_178335.2 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:1940245 C>G maps to NM_133335.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:5827254 G>A maps to NM_001014809.1 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:38910247 G>A maps to NM_138389.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:39116802 G>A maps to NM_015990.4 W688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:40245011 G>C maps to NM_004310.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:55968636 G>A maps to NM_002253.2 Q676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:57179511 G>A maps to NM_020722.1 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:76817436 C>T maps to NM_006239.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:76882203 G>A maps to NM_018115.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:82065387 C>T maps to NM_006259.1 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:95201921 G>A maps to NM_001128429.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:102981530 G>C maps to NM_017935.4 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:111430910 C>G maps to NM_001977.3 S381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:140646941 C>G maps to ENST00000509479 R793R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:154517429 C>T maps to NM_001131007.1 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr4:169602527 C>G maps to NM_001166108.1 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:155045 G>A maps to NM_052909.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:5239962 C>T maps to NM_139056.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:6605469 C>T maps to NM_017755.5 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:36035958 G>A maps to NM_174914.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:37174002 G>A maps to NM_023073.3 L2009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:55407500 C>T maps to NM_024669.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:56178365 C>T maps to NM_005921.1 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:76171198 C>T maps to NM_130772.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:112174756 G>T maps to NM_001127510.2 E1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:124036728 G>A maps to NM_020747.2 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:133747453 G>C maps to NM_080656.2 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140432122 C>A maps to NM_013340.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140594402 C>T maps to NM_018933.2 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140753991 G>A maps to NM_018919.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:140779097 G>A maps to NM_018925.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:141325350 C>T maps to NM_016580.2 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:149754545 C>T maps to ENST00000451292 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:150110696 C>T maps to NM_001135643.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:150947808 C>T maps to NM_001447.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:154308187 C>T maps to NM_015465.3 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:170222426 C>G maps to NM_014211.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr5:173040144 C>T maps to NM_138369.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:3285314 G>C maps to ENST00000436008 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:11190712 G>C maps to NM_006403.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:24865636 G>C maps to NM_014722.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:24873897 G>C maps to NM_014722.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:26056379 G>A maps to NM_005319.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:26199438 G>A maps to NM_021065.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:26411781 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:27860614 G>A maps to NM_003514.2 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:29454595 G>A maps to NM_052967.1 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:29556416 G>A maps to NM_007160.3 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:30131830 C>T maps to NM_033229.2 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:30881723 C>T maps to NM_001517.4 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:32150063 G>A maps to ENST00000375070 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:34101144 G>A maps to NM_000841.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:35216388 C>T maps to ENST00000394681 F979F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:35706279 C>T maps to NM_145028.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:37426533 C>T maps to NM_015050.2 F308F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:50805696 G>A maps to ENST00000263046 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:73843258 G>T maps to NM_001160133.1 E474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:86256944 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:108496092 G>A maps to ENST00000368983 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:128410864 C>A maps to ENST00000368210 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:139186274 C>T maps to NM_001195037.2 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:152651319 G>A maps to NM_182961.2 R4834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:152651533 C>T maps to NM_182961.2 L4762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr6:160477478 C>G maps to NM_000876.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:1521035 G>A maps to ENST00000389470 F1431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:5569264 G>T maps to NM_001101.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6189332 C>T maps to ENST00000404835 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6624734 C>A maps to NM_018106.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6730898 G>A maps to ENST00000330442 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:6732257 G>A maps to ENST00000330442 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:30492525 G>A maps to NM_006092.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:33392469 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:44193017 C>T maps to NM_000162.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:48311968 C>G maps to NM_152701.3 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:75172290 C>T maps to NM_005338.4 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:76027117 C>T maps to NM_080744.1 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:92147126 C>T maps to NM_000466.2 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:99364027 C>T maps to NM_017460.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:100212804 G>A maps to NM_023948.4 *236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:107599731 C>T maps to NM_002291.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:128490514 G>A maps to NM_001458.4 A1792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:143632801 G>A maps to NM_001004685.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr7:150327200 G>C maps to ENST00000438845 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:10468838 G>A maps to NM_178857.5 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:62438578 C>T maps to NM_004318.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:70585256 G>A maps to NM_030958.2 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:95892356 C>T maps to NM_017864.2 I961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:110510689 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:121383404 C>T maps to NM_021110.1 Q1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:121514759 A>G maps to NM_022045.3 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:125487427 C>G maps to NM_007218.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:125487526 C>G maps to NM_007218.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:141810663 C>A maps to NM_005607.4 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:144668985 C>T maps to NM_032378.4 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr8:144947097 C>T maps to NM_031308.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:14313492 G>A maps to ENST00000397581 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:33948388 G>T maps to NM_018449.2 S418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:34257246 C>T maps to NM_194313.2 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:124906607 G>C maps to NM_014222.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:125621300 C>A maps to NM_001100588.1 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:129870632 C>T maps to NM_012098.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:130434371 C>T maps to NM_003165.3 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:130494387 G>A maps to NM_001085347.1 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:131087435 C>T maps to NM_016035.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:132630420 G>C maps to NM_001008563.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:134308164 C>T maps to NM_013318.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chr9:136507467 C>G maps to NM_000787.3 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:10106774 C>T maps to NM_015691.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:14708968 G>A maps to NM_002063.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:19369481 C>T maps to NM_001173454.1 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:41203032 G>A maps to NM_001356.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:48650255 C>T maps to NM_002049.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:50129584 C>G did not map to a codon.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:55051211 C>T maps to NM_000032.4 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:109416483 G>A maps to NM_032227.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:141291071 C>T maps to NM_016249.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:152958596 C>G maps to NM_005629.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I4-01A-11D-A21A-08 chrX:154088778 C>T maps to NM_000132.3 V2276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:18152534 C>T maps to NM_030812.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:20107203 C>T maps to NM_181719.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:22165876 G>A maps to NM_005529.5 I3292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:23782406 G>A maps to NM_017707.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:27332435 C>G maps to NM_052943.3 *426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:28290196 C>T maps to NM_018053.2 Y161Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:29095439 G>A did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:47181985 G>A maps to NM_014774.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:66102577 T>C maps to NM_002303.5 N1126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:145474161 G>T maps to NM_001039888.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:167906232 G>A maps to ENST00000367840 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:169519104 G>A maps to ENST00000367796 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:169845136 A>C maps to NM_181093.2 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:200954054 C>T maps to NM_017596.2 R1245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:227152912 C>T maps to NM_020247.4 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:248112659 T>C maps to NM_001001963.1 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr1:248224483 T>C maps to NM_001004687.1 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr10:24880172 G>A maps to NM_020824.3 V1377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr10:85973932 C>T maps to NM_033100.2 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr10:123845773 G>A maps to NM_206862.2 V1253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:1028661 G>A maps to NM_005961.2 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:12525870 C>T maps to NM_018222.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:46920515 G>A maps to ENST00000256991 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:118342390 C>T maps to NM_001197104.1 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr11:130785627 G>A maps to NM_014758.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:7635262 G>A maps to NM_004244.4 R1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:25149237 G>A maps to NM_001101339.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:51639757 G>T maps to NM_001031628.1 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:53040645 C>G maps to NM_000423.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:56091543 A>G maps to ENST00000347027 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr12:94965477 C>T maps to NM_020698.2 K389K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr13:99908093 G>C maps to NM_005292.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr14:23559766 G>A maps to NM_014977.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr14:32562940 T>C maps to NM_001030055.1 H1022H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr14:104174928 G>A maps to NM_005432.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:28460862 C>T maps to NM_004667.4 Q2038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:40660106 C>T maps to NM_033510.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:76017545 G>A maps to NM_175881.3 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr15:83710669 G>C maps to NM_025238.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:48130785 G>A maps to NM_033226.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:68269813 C>G maps to NM_024939.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr16:89958627 C>T maps to NM_014972.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:5087089 T>G maps to NM_032530.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:5371894 G>A maps to ENST00000457531 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:7121569 G>C maps to NM_001365.3 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:32964389 C>T maps to NM_207313.1 T698T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:37947791 G>A maps to NM_012481.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:44076788 C>T maps to NM_001007532.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:48153805 C>T maps to NM_002204.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:48545625 C>T maps to NM_001267.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr17:77808681 G>C maps to NM_003655.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:1796869 G>C maps to NM_138813.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:4338735 C>T maps to ENST00000314714 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:6836571 G>A maps to NM_005428.2 W636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:17321179 G>A maps to NM_004145.3 E1929E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:34884958 G>T maps to NM_000175.3 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:35505211 C>T maps to NM_020895.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:38055988 A>G maps to NM_016536.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:41223369 G>A maps to NM_025194.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr19:50311870 C>T maps to NM_025129.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:39499673 G>A maps to NM_003618.2 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:79312627 A>C maps to NM_006507.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:80646671 G>A maps to ENST00000402739 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:179433785 A>G maps to NM_133378.4 D23123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:196877530 G>A maps to NM_018897.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:201757013 T>A maps to NM_001136039.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:219920153 T>G maps to NM_002181.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:234580785 C>A maps to ENST00000373460 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr2:238283322 G>A maps to NM_004369.3 I1137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr20:3781634 G>A maps to NM_021873.2 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr20:52774034 C>T maps to NM_000782.4 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr21:37603049 C>T maps to NM_005128.2 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr22:19462609 G>A maps to ENST00000399525 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr22:19965030 G>A maps to NM_001670.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:13363765 C>T maps to NM_024923.2 Q1614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:48463745 C>T maps to NM_001130082.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:50379287 C>T maps to NM_015896.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:52404220 C>T maps to ENST00000273600 F2078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:58178461 G>A maps to NM_004944.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:121413221 G>A maps to ENST00000393667 L2050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:151545956 A>G maps to NM_001086.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:159482389 G>A maps to NM_001197113.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr3:184040228 C>T maps to NM_001194947.1 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:2927795 G>T maps to NM_014189.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:54231439 G>A maps to NM_152540.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:54967809 G>T maps to NM_133267.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:100237198 G>A maps to NM_000668.4 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr4:153573936 C>A maps to NM_152680.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr5:40681892 C>G maps to NM_000958.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr5:176830945 G>A maps to NM_000505.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr5:176831564 G>A maps to NM_000505.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr6:4059020 C>T maps to NM_003913.4 Y931Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr6:7211054 G>A maps to NM_001003699.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr6:22297249 G>C did not map to a codon.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr6:24433444 G>A maps to NM_001503.2 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:73097378 G>A maps to NM_032317.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:75178215 A>T maps to NM_005338.4 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:75178224 A>C maps to NM_005338.4 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:99032711 G>A maps to NM_001198879.1 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:126086315 C>T maps to NM_001127323.1 Q847Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr7:157160088 A>G maps to NM_058246.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr8:72959439 T>C maps to NM_007332.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:123151528 G>A maps to NM_018249.4 S1889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:123169488 G>A maps to NM_018249.4 F1588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chr9:125009804 G>A maps to NM_033117.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:9900214 A>G maps to NM_001649.2 R964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:19014181 C>G maps to NM_001079858.2 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:19389507 C>T maps to NM_001001671.3 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:99919816 C>A maps to NM_014467.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:135431714 G>C maps to NM_153834.3 G1950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:147014277 A>G maps to NM_002024.5 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A2I6-01A-12D-A18F-08 chrX:153043510 C>T maps to NM_005393.2 F1790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:23763472 G>C maps to NM_017707.3 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:27107007 C>T maps to NM_006015.4 Q2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:112309337 G>A maps to NM_007204.4 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:114680319 G>A maps to ENST00000369545 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr10:104142017 C>T maps to NM_004193.2 I1835I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr11:68525171 C>G maps to NM_001876.3 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr11:124763843 G>C maps to NM_019055.5 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:247680 G>A maps to NM_001170738.1 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:1702938 G>A maps to NM_152441.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:102158443 G>A maps to NM_024312.4 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:105440690 C>T maps to NM_001034173.3 K581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr12:114836394 G>A maps to NM_000192.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr15:34646668 C>G maps to ENST00000438749 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr15:91475080 C>A maps to ENST00000394272 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr17:4642108 C>G maps to NM_001100812.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr17:49340654 G>C maps to NM_016001.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr17:73486836 C>T maps to ENST00000375248 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:1584562 C>T maps to NM_003926.5 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:5824094 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:41386395 G>T maps to NM_000764.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:44223732 G>A maps to NM_019612.3 E341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:46216735 G>A maps to NM_001080469.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr19:55106714 C>G maps to NM_006863.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:234212 G>C maps to NM_015677.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:16747024 A>G maps to NM_030797.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:98340714 C>T maps to NM_001079.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr2:231081528 T>C maps to NM_080424.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr20:35865106 C>G maps to NM_002951.3 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr20:36572408 C>T maps to NM_080607.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr21:31852399 C>T maps to NM_181607.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr21:46021231 C>G maps to ENST00000380102 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:9956435 C>G maps to NM_153483.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:39225688 G>A maps to NM_194293.2 L1750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:45800487 G>A maps to NM_020208.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:155215190 C>T maps to ENST00000340059 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr3:195610066 G>A maps to NM_001010938.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:72400083 C>T maps to NM_001098484.2 N807N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:89385091 G>T maps to NM_016323.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:129778585 G>T maps to NM_199320.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:141888842 G>T maps to NM_020724.1 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr4:158281082 C>T maps to NM_000826.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr5:150889706 G>A maps to NM_001447.2 F3978F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr5:176308337 C>G maps to NM_002115.2 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:18212780 G>A maps to ENST00000388870 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:30459139 G>C maps to NM_005516.5 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:160210476 G>A maps to NM_030752.2 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr6:168272963 C>G maps to ENST00000400822 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:12668811 C>G maps to NM_001112706.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:84671544 G>C maps to NM_152754.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:99227061 G>T maps to NM_145115.2 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr7:147600710 G>A maps to NM_014141.5 W718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:42586932 G>T maps to NM_000749.3 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:48846650 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:72755903 G>A maps to NM_005098.3 N170N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:95186396 G>A maps to NM_001144663.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr8:101721412 A>G maps to NM_002568.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:114296105 G>T maps to NM_133464.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:131387391 G>A maps to NM_001130438.2 E2001E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:131553893 G>C maps to NM_018201.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chr9:140354927 C>A maps to NM_001098537.1 E1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IK-01A-32D-A21A-08 chrX:102931202 T>C maps to NM_001142432.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:26349271 C>T maps to NM_004455.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:26610894 G>A maps to NM_183008.2 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:37270761 C>T maps to NM_000831.3 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:165175151 G>A maps to NM_177398.3 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:165532871 C>T maps to NM_001005214.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:202709879 T>C maps to ENST00000367264 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr1:204511993 G>A maps to NM_002393.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr10:38241660 C>T maps to NM_145011.2 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:800220 C>T maps to NM_145886.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:76796097 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr11:108009665 T>C maps to NM_000019.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr13:70314575 G>A maps to NM_020866.2 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr15:77323594 C>T maps to NM_003978.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr15:101595286 T>A maps to NM_024652.3 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:4764076 C>G maps to NM_133450.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:28834729 G>T maps to NM_148414.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr16:82891975 C>T maps to ENST00000268613 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:7802504 C>T maps to NM_001005271.2 Y835Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:10608308 C>T maps to NM_020233.4 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:30348422 G>C maps to ENST00000327564 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr17:79612040 C>T maps to NM_031945.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:11660486 C>A maps to NM_001299.4 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:50961862 C>G maps to NM_004533.3 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr19:59028485 T>C maps to NM_032792.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr2:49189907 G>A maps to NM_000145.3 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr2:85894866 C>A maps to NM_198843.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr2:175979452 T>C maps to NM_001880.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr22:16449132 A>C maps to NM_001005239.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr22:40804818 C>T maps to NM_015705.4 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr3:44685244 G>T maps to NM_006991.3 E875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr3:119120885 G>A maps to NM_020754.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr3:190366313 G>A maps to NM_002182.3 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:951683 G>T maps to NM_032326.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:57842716 G>T maps to NM_032313.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:170988518 T>C maps to ENST00000509167 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr4:187525599 C>A maps to ENST00000260147 P3496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr5:1294370 G>A maps to NM_198253.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr6:139097340 C>A maps to NM_015439.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr7:20199458 C>T maps to NM_182762.3 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr7:128471002 C>G maps to NM_001458.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chr8:11615911 G>A maps to NM_002052.3 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chrX:32383165 G>T maps to ENST00000357033 R1666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chrX:35993360 G>A maps to NM_152632.3 Q784Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chrX:107331993 A>G maps to NM_002814.2 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chrX:117054333 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chrX:131233526 C>T maps to NM_194277.2 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IL-01A-11D-A20D-08 chrX:153038979 C>T maps to NM_005393.2 R1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:6219572 C>T maps to NM_015557.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:27087416 C>G maps to NM_006015.4 S664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:42925521 A>G maps to NM_024664.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:101705631 C>T maps to NM_001400.4 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:152277089 G>A maps to NM_002016.1 H3424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:152283896 G>A maps to NM_002016.1 H1155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:170961421 G>A maps to NM_001163629.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr1:210334176 T>C maps to NM_001146261.1 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr10:3823884 C>T maps to NM_001300.5 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr10:3824276 C>A maps to NM_001300.5 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr10:99133482 G>A maps to NM_015179.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr11:61959666 C>T maps to NM_006552.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr11:62393904 T>A maps to NM_198335.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:28116291 C>T maps to ENST00000354417 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:49424740 G>A maps to NM_003482.3 R4536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr12:62148676 G>A maps to NM_178539.3 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr13:103053995 A>T maps to NM_175929.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr17:7329762 C>T maps to NM_175734.4 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr18:53254338 G>A maps to ENST00000398339 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr19:2403104 C>T maps to NM_182973.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr19:9061675 C>T maps to NM_024690.2 V8590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr19:44129329 G>A maps to NM_145296.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr2:100623237 C>T maps to NM_001025108.1 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr20:35724277 C>A maps to NM_002895.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr20:57767396 C>T maps to NM_178457.1 D441D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr3:122446796 C>T maps to NM_017554.2 R1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr3:123419211 G>A maps to NM_053025.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:1313342 C>A maps to NM_033260.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:154412525 G>A maps to NM_001145279.1 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr6:160517636 C>T maps to NM_000876.2 T2274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr7:143657848 C>G maps to NM_012369.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr8:2830726 G>T maps to NM_033225.5 S2945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr8:22475218 G>A maps to NM_021174.5 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr9:7103806 G>A maps to NM_015061.3 E849E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr9:111665222 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chr9:139369742 C>T maps to NM_014866.1 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chrX:7870170 G>A maps to NM_001142389.1 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chrX:102334725 G>A maps to NM_022052.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IM-01A-11D-A20D-08 chrX:104463695 C>A maps to NM_031274.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:1417557 G>A maps to NM_031921.4 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:11008901 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:17586129 C>T maps to NM_016233.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:27100194 C>T maps to NM_006015.4 Q1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:33292239 G>A maps to NM_022753.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:35251004 C>G maps to NM_001005752.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:37319266 C>T maps to NM_000831.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:54692804 C>T maps to NM_145716.2 *389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:62728782 C>T maps to NM_181712.4 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:111674047 G>A maps to NM_178454.4 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:150307519 G>C maps to NM_004698.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:159827691 C>A maps to NM_001013661.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:161044086 G>C maps to NM_030916.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:167059488 G>C maps to NM_005814.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:203696674 G>A maps to NM_001001396.1 R1095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:205492647 G>A maps to NM_212503.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr1:222717297 C>T maps to NM_024746.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:15120549 C>G maps to NM_001039844.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:71716779 C>G maps to ENST00000356340 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:81373715 C>T maps to NM_001093770.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr10:88939997 G>A maps to ENST00000298786 E779E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:4388658 C>T maps to NM_001005161.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:13732281 G>A maps to NM_032228.5 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:48185098 C>T maps to NM_002843.3 I1216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:57003560 G>A maps to NM_005161.4 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:58893518 C>G maps to NM_198947.3 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:59190321 G>C maps to NM_001001954.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:63312135 G>A maps to NM_004585.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:73102215 C>T maps to NM_152222.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:92534005 C>T maps to ENST00000298047 V2609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:119545905 G>A maps to NM_002855.4 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr11:133792551 G>A maps to NM_014987.1 I731I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:11183790 G>C maps to NM_176885.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:46761068 C>T maps to NM_018976.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:49434739 G>T maps to NM_003482.3 P2271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:51634656 C>T maps to NM_014764.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:51759226 G>A maps to NM_007210.3 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:55725669 C>T maps to NM_054104.1 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:56351374 G>A maps to NM_006928.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:72666767 G>C maps to NM_013381.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:104190737 G>A maps to NM_001031701.2 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:118533367 G>A maps to NM_019086.5 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:120884566 C>T maps to NM_176818.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:120995452 G>A maps to ENST00000458409 W312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:130919335 G>A maps to NM_015347.4 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:132502127 C>T maps to ENST00000333577 I1360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr12:132522553 G>A maps to ENST00000333577 P2076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr13:49039353 C>A maps to NM_000321.2 S780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr13:58208644 G>A maps to NM_001040429.2 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr14:24647295 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr14:75230696 C>T maps to NM_019589.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:42703969 G>C maps to NM_000070.2 *822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:65681730 G>T maps to NM_020962.1 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:75112415 C>T maps to NM_021819.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr15:78346478 C>T maps to NM_144572.1 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:716289 C>T maps to NM_145294.4 F1560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:2495467 G>A maps to NM_001761.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4924306 G>C maps to NM_016936.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4933974 G>A maps to NM_002705.4 L1561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4934724 G>A maps to NM_002705.4 L1311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:4934736 C>A maps to NM_002705.4 E1307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:16110411 C>T maps to ENST00000399408 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:27460068 C>G maps to NM_181079.4 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:30005478 C>T maps to NM_003609.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:57250817 G>T maps to NM_133368.1 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:57789143 C>T maps to NM_005886.2 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:57789808 G>C maps to NM_005886.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr16:68909057 G>A maps to NM_024562.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:15522809 G>C maps to ENST00000261644 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:27413463 G>A maps to NM_078471.3 L1948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:33807128 G>A maps to ENST00000361112 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:38178926 G>C maps to NM_014815.3 L801L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:39394330 C>T maps to NM_031963.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:40021194 C>T maps to NM_018143.1 W143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:41246521 C>G maps to ENST00000471181 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:42759436 G>C maps to NM_144609.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:44630809 C>T maps to NM_001006607.2 F1618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr17:62499952 G>A maps to NM_004396.3 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:5745952 C>A maps to NM_152784.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:5941639 G>C maps to NM_007322.2 S133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:6389528 G>A maps to NM_002096.2 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:9001861 C>G maps to NM_024690.2 S13462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:12296679 C>G maps to NM_003437.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:12911833 G>A maps to NM_005809.4 C51C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:15734172 C>T maps to NM_007253.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:17411696 C>T maps to NM_024527.4 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:35250829 G>A maps to NM_001007248.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:39399437 C>G maps to NM_002503.3 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:45767942 G>A maps to NM_031417.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:48244214 G>A maps to NM_014601.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:49967511 G>A maps to NM_153329.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:54973626 C>T maps to NM_198988.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr19:55294989 G>A maps to ENST00000291633 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:25803617 G>A maps to NM_021907.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:73160998 G>A maps to NM_004097.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:96047360 C>T maps to NM_013434.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:96809648 G>A maps to NM_004418.3 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:101188177 G>A maps to NM_024065.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:120439082 C>T maps to NM_030577.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:201305421 C>T maps to ENST00000409151 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:202149750 C>T maps to NM_001080125.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:202755539 C>T maps to ENST00000450471 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:206023471 C>G maps to ENST00000406610 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:206023537 C>A maps to ENST00000406610 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:228882209 C>G maps to NM_001142644.1 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr2:233431864 A>G maps to NM_004846.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:13765903 G>T maps to NM_024120.4 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:18513306 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:42969879 C>T maps to NM_178491.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:48500482 C>T maps to ENST00000417961 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr20:61574869 C>T maps to NM_017896.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr21:32519222 G>T maps to NM_003253.2 V1155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:24761540 G>A maps to NM_015330.2 Q975Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:32017072 G>C maps to ENST00000422296 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:32626964 C>G maps to NM_014227.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr22:35947614 C>T maps to NM_014310.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:38042960 G>A maps to NM_015873.3 Q399Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:38043071 G>T maps to NM_015873.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:38043287 G>A maps to NM_015873.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:39374253 G>A maps to NM_005201.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:124356150 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:133374176 C>T maps to NM_007027.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr3:184026527 G>A maps to NM_002808.3 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:57367867 G>C maps to NM_006947.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:87694008 G>A maps to NM_080685.2 S1754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:153244234 G>C maps to NM_033632.2 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:174254743 G>A maps to NM_002129.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr4:190884259 G>A maps to NM_004477.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr5:13823434 G>C maps to NM_001369.2 L2208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr5:139781719 C>T maps to ENST00000253810 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:20490416 C>G maps to NM_001949.3 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:26508196 C>T maps to NM_001732.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:32164148 G>A maps to NM_004557.3 A1750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:43251282 G>A maps to NM_032538.1 E935E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:53138101 G>A maps to ENST00000370918 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:86253326 T>C maps to NM_153816.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:107365502 G>A maps to NM_001142470.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:107780312 G>A maps to NM_020381.3 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:157803262 C>T maps to NM_024630.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr6:167709657 G>A maps to NM_018974.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr7:6472551 G>A maps to NM_139179.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr7:86569359 G>C maps to NM_001142749.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr7:98256481 G>T maps to NM_002523.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:1893768 C>G maps to ENST00000398564 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:8750148 G>A maps to NM_004225.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:31015038 C>T maps to NM_000553.4 V1325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:101270980 G>A maps to NM_183419.1 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:125579321 G>C maps to NM_014751.4 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:135524802 G>C maps to NM_020863.3 L1092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr8:143570747 G>A maps to NM_001702.2 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:36118869 C>T maps to NM_021111.2 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:75366835 C>T maps to NM_138691.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:79320826 G>A maps to NM_015225.2 L2121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:91667004 G>C maps to NM_016848.5 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:130496589 G>A maps to NM_001085347.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IN-01A-11D-A20D-08 chr9:139090905 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:3640002 G>A maps to NM_005427.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:16133951 C>A maps to NM_001089591.1 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:27623587 C>T maps to ENST00000319394 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:50642769 T>G maps to NM_021952.3 L87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:64095754 C>T maps to NM_002633.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr1:116931579 C>T maps to NM_000701.7 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr10:102789912 G>A maps to NM_001195263.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr10:118321148 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:408081 G>A maps to NM_021805.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:720213 C>T maps to NM_022772.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:46567155 G>C maps to ENST00000458649 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:46567256 G>A maps to ENST00000458649 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:61026230 G>C maps to NM_152718.2 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:64855480 C>T maps to NM_006782.3 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:70003069 G>A maps to NM_018043.5 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:92616260 C>T maps to ENST00000298047 R4213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr11:113683112 G>A maps to NM_020886.2 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:15815013 A>G maps to NM_004447.5 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:53044193 G>A maps to NM_000423.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:58017660 C>T maps to NM_133489.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:62783260 A>G maps to ENST00000280377 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr12:66770814 C>T maps to ENST00000359742 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr13:32745307 G>A maps to NM_023037.2 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr13:114077229 G>A maps to NM_138430.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr14:100795894 C>G maps to NM_207117.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr15:59500903 G>A maps to NM_004998.2 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr16:3293383 C>T maps to NM_000243.2 A701A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:2601719 G>A maps to NM_015229.3 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:63173908 C>G maps to NM_003835.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:72233572 C>G maps to NM_032646.5 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:72781646 C>T maps to NM_017728.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr17:73512920 C>T maps to NM_207346.2 Q51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr19:11213401 C>T maps to NM_000527.4 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:44036904 G>A maps to NM_001193464.1 *353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:54876993 G>A maps to NM_003128.2 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:73315527 C>G maps to NM_015470.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:179575376 G>A maps to NM_133378.4 Q8239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:190640310 G>A maps to NM_016467.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr2:233655997 C>A maps to ENST00000373566 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:422525 C>A maps to ENST00000246077 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:23966390 G>T maps to NM_178311.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:36959491 G>A maps to NM_001725.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:37182715 G>A maps to NM_020336.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:43940279 G>A maps to NM_014276.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr20:60878629 G>A maps to NM_175573.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr21:32617836 G>A maps to NM_003253.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr21:47850002 G>A maps to NM_006031.5 E2590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr21:47851759 G>A maps to NM_006031.5 L2794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr22:50192220 G>A maps to ENST00000342989 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:13916515 G>A maps to NM_004625.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:49756010 C>T maps to NM_198722.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:122667458 G>A maps to NM_001031702.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:129290521 G>C maps to NM_015103.2 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr3:137888978 C>G maps to NM_016216.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr4:2934900 G>A maps to NM_001146069.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr4:42403248 G>C maps to NM_001080505.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr4:126237763 G>C maps to NM_024582.4 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:9629538 C>T maps to NM_019599.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:36049522 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:45303767 G>A maps to NM_021072.2 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:132198222 T>C maps to NM_005260.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:134023940 C>T maps to NM_021982.1 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:140175187 G>T maps to NM_018905.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr5:168100245 T>C maps to NM_003062.2 P1259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:1390559 C>A maps to NM_001452.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:32015616 C>T maps to ENST00000375244 R3406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:35426106 C>T maps to NM_021922.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:35923091 G>C maps to NM_052961.3 S690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:46607285 C>A maps to NM_016593.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr6:116436851 A>G did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr7:107329645 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr8:124383929 C>A maps to NM_014109.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr9:115950729 A>G maps to ENST00000446284 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IQ-01A-31D-A20D-08 chr9:136220671 G>A maps to NM_003172.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:28477481 G>C maps to NM_001164721.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:35851046 C>G maps to NM_005095.2 S525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:51736895 C>T maps to NM_014372.4 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:60139744 C>G maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:109271378 C>T maps to NM_001144937.1 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:151261979 C>G maps to NM_020832.1 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:152187696 G>A maps to NM_001009931.1 H2136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:155921969 G>A maps to NM_001162383.1 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:162745931 C>G maps to NM_006182.2 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr1:237806718 C>T maps to NM_001035.2 I2438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:50532110 G>A maps to NM_001135196.1 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:60148580 T>G did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:64968349 G>A maps to NM_032776.1 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:70044040 G>A maps to NM_022129.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr10:135204913 C>T maps to NM_152911.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:2436596 C>T maps to ENST00000452833 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:17757752 G>A maps to NM_001112741.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:27077156 G>A maps to NM_003986.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:62439584 G>A maps to NM_001085372.2 *94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:78516496 G>A maps to NM_001098816.2 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:94533412 C>T maps to NM_130847.2 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:111946330 G>T maps to NM_018195.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:118416127 G>C maps to NM_020153.3 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:119003646 G>T maps to NM_198971.1 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:122931882 C>T maps to NM_006597.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:123900526 C>T maps to NM_001004464.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:126294663 G>T maps to NM_032531.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:130066274 C>T maps to NM_021978.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr11:132184469 G>A maps to NM_001144058.1 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:14975925 C>T maps to NM_175874.3 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:19427758 C>G maps to ENST00000429027 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:53227585 G>A maps to NM_175834.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:53227663 G>C maps to NM_175834.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:56345847 C>T maps to NM_201554.1 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:56717845 G>C maps to NM_001127460.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:104388222 G>A maps to NM_031302.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:109872911 C>T maps to NM_001101421.3 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:114392941 G>A maps to NM_016196.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:117595694 G>A maps to NM_033624.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:123214481 G>A maps to NM_032554.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:124415936 C>G maps to NM_207437.3 L4160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr12:125451374 C>T maps to NM_032656.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr13:23909329 G>A maps to NM_014363.4 N2895N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr13:23915752 G>A maps to NM_014363.4 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr13:75933987 G>A maps to ENST00000431480 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr14:90437608 C>T maps to NM_018319.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr14:94914895 G>A maps to NM_001080451.1 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr14:102606454 C>G maps to ENST00000454394 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:41624730 G>C maps to NM_007280.1 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:52090494 G>A maps to NM_014548.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:75798200 G>A maps to NM_002833.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:89398557 G>A maps to NM_013227.3 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr15:91025470 G>A maps to NM_003870.3 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:2042985 C>T maps to NM_004209.5 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:31383089 C>T maps to NM_000887.3 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:66766330 G>C maps to NM_006141.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:75579279 C>T maps to NM_001077416.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr16:86544387 G>A maps to NM_001451.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:7797533 C>T maps to NM_001005271.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:27903632 C>T maps to NM_001085454.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:34261800 C>T maps to NM_020426.1 *149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:36955629 G>C maps to NM_003559.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:37564543 C>T maps to NM_004774.3 L1310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:37879819 G>A maps to NM_004448.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:40370257 C>T maps to NM_012448.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:41606895 C>T maps to NM_001079675.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:43912039 G>A maps to NM_001145146.1 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:59981822 G>A maps to NM_020748.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:66430740 G>A maps to NM_017983.5 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:67255905 G>C maps to ENST00000392677 L1225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:73759153 G>A maps to ENST00000437911 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:79170816 C>A maps to ENST00000269392 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr17:80478009 C>T maps to NM_004514.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr18:44260397 C>T maps to NM_013305.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr18:45556269 C>T maps to NM_001039360.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr18:59954629 G>A maps to NM_020854.3 Q1100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:3938611 C>T maps to NM_170678.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:7986330 C>G maps to NM_003083.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:9082527 G>T maps to NM_024690.2 S3096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:9868233 C>A maps to NM_001077624.1 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:11123776 C>T maps to NM_001128849.1 I809I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:15806820 C>T maps to NM_023944.2 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:21990729 C>T maps to NM_003423.2 E703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:45375332 C>T maps to NM_001042724.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:45899847 G>A maps to NM_001142502.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:47597705 C>T maps to NM_015168.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:50926887 G>A maps to NM_003121.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:53384364 G>A maps to NM_207333.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr19:54313766 C>T maps to ENST00000391773 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:27465811 C>T maps to NM_004341.3 R2151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:27858050 G>A maps to NM_007266.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:54880915 C>T maps to NM_003128.2 F1916F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:220041502 G>A maps to NM_015680.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:220470930 G>C maps to NM_052902.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr2:230661453 G>A maps to ENST00000389044 V1196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:1433190 C>A maps to ENST00000476071 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:5927103 C>T maps to NM_015939.3 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:9520183 G>A maps to NM_177990.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:44984458 G>T maps to NM_173179.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr20:50769824 G>C maps to NM_018197.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr21:46020559 G>A maps to ENST00000380102 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr21:47419593 G>A maps to NM_001848.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr22:18561372 G>C maps to ENST00000399743 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr22:19709360 T>C maps to NM_002688.5 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr3:25805629 G>C maps to NM_018297.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr3:52730303 G>A maps to NM_018446.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr3:101060618 G>C maps to NM_020654.3 S704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:1985606 G>A maps to NM_005663.3 Q435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:2130960 C>G maps to NM_181808.2 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:6925316 G>A maps to NM_001113361.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:89671698 G>A maps to NM_014883.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:106510537 C>G maps to ENST00000420470 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:106603931 C>T maps to NM_020395.3 Q449Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr4:147754964 G>A maps to ENST00000513335 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:16453157 G>A maps to NM_033414.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:33751569 C>T maps to NM_030955.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:55178998 C>T maps to NM_139017.4 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:64967756 G>C maps to NM_019072.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:122364491 G>A maps to NM_000943.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:140222357 G>A maps to NM_018911.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:141314120 G>A maps to NM_014773.3 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:148999930 C>T maps to NM_001001669.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr5:149498308 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:32362584 G>A maps to ENST00000468270 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:32821185 G>A maps to NM_000593.5 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:34499550 C>G maps to NM_020804.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:44233272 C>T maps to NM_004556.2 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:132909812 C>G maps to NM_003967.2 *338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:150209696 G>A maps to NM_139165.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr6:150210553 G>C maps to NM_139165.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:44664044 C>T maps to ENST00000444676 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:47454804 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:77011906 C>T maps to NM_017439.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:100382357 G>A maps to ENST00000349350 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:142983918 T>C maps to NM_153345.1 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr7:151891213 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:1645431 C>T maps to ENST00000357934 N914N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:8749554 G>A maps to NM_004225.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:23290507 C>T maps to NM_004901.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:64099963 C>T maps to ENST00000339066 F464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:71068648 G>A maps to NM_006540.2 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:75272519 G>T maps to NM_018972.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:103301749 G>T maps to NM_015902.4 I1548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:131138242 G>A maps to NM_018482.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr8:144411591 A>G maps to NM_052963.1 Y96Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:15472666 G>A maps to NM_001128217.1 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:35805554 C>G maps to NM_003995.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:94172287 G>A maps to NM_005384.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:100845192 C>T maps to NM_018946.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chr9:131342007 G>A maps to NM_001130438.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:29959766 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:44894181 C>T maps to NM_021140.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:70099854 C>A maps to NM_001003811.1 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:70360616 A>G maps to ENST00000333646 Q2062Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:123197010 C>T maps to NM_001042750.1 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:124097479 G>A maps to NM_001163278.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:151123199 G>C maps to NM_004961.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:151303447 C>T maps to NM_021048.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IS-01A-21D-A21A-08 chrX:152770151 G>A maps to NM_001711.4 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:23395117 C>T maps to NM_001009999.2 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:35250590 C>T maps to NM_001005752.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:40529929 C>G maps to NM_001105530.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:87208004 C>A maps to ENST00000482504 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:115262242 G>A maps to NM_001130523.1 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:146672878 G>C maps to NM_001461.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:147092561 G>A maps to NM_004326.2 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:153713792 C>A maps to ENST00000428986 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:156386656 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:156617354 G>A maps to NM_021948.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:158724898 G>A maps to NM_001005184.1 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:160098494 G>A maps to NM_000702.3 K357K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:203680025 G>A maps to NM_001001396.1 R607R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr1:214815001 G>A maps to NM_016343.3 Q1107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:50966536 G>A maps to NM_018245.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:68687369 G>A maps to NM_178011.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:72324121 G>A maps to NM_014431.2 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:100249920 C>G maps to NM_021828.4 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:105207265 G>C maps to NM_015916.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:129537069 G>A maps to NM_207426.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr10:134459391 G>A maps to NM_005539.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:33370176 C>T maps to NM_005734.3 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:56258213 G>A maps to NM_001005282.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:62398116 G>A maps to NM_198335.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:70332668 G>A maps to ENST00000338508 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:85961446 C>G maps to ENST00000351625 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:94316612 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:107673744 G>C maps to NM_017515.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr11:111594444 C>G maps to NM_015191.1 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:48375125 C>T maps to NM_001844.4 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:52574305 G>T maps to NM_182507.2 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:53165705 G>C maps to NM_015848.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:72312285 C>T maps to NM_022771.4 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:78400994 G>A maps to NM_014903.4 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr12:132404536 G>C maps to NM_003565.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:31205592 C>T maps to NM_005800.4 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:32808827 C>A maps to NM_023037.2 S1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:39540962 C>T maps to NM_145286.2 *292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:72053448 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr13:79190192 G>C maps to NM_024546.3 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:21991094 G>A maps to NM_005407.1 Q923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:23530571 G>C maps to NM_014977.3 S1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:54950454 C>A maps to NM_004124.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:58831817 C>G maps to NM_002892.3 S1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:102551298 C>A maps to NM_001017963.2 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:105173275 C>G maps to ENST00000252520 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr14:105174217 C>A maps to ENST00000252520 I538I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:77770686 G>T maps to NM_018200.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:86064774 C>T maps to NM_006738.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:88576242 G>C maps to NM_001012338.1 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr15:90348335 C>T maps to NM_001150.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:624460 C>T maps to NM_148920.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:31391115 C>T maps to NM_000887.3 I969I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:67218810 G>A maps to NM_178516.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:67876897 G>T maps to NM_020457.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr16:83948928 G>T maps to NM_012213.2 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:5041506 C>T maps to NM_004505.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:6374546 C>A maps to NM_031220.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:7010562 G>A maps to NM_080912.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:38297459 G>T maps to NM_007359.4 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:39017932 C>A maps to NM_000223.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:42849818 G>C maps to NM_002390.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:43522897 C>G maps to NM_014798.2 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:48604700 C>T maps to NM_032133.4 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:61994707 G>A maps to NM_000515.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:62854902 G>C maps to NM_199340.2 L1601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr17:79517598 C>T maps to NM_025161.5 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr18:43216987 C>T maps to NM_007163.3 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr18:58038832 C>T maps to NM_005912.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:6392881 G>A maps to NM_002096.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:8436323 C>G maps to NM_139314.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:16860124 C>G maps to ENST00000438489 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:36108217 G>T maps to NM_015302.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:46345717 G>A maps to NM_004819.2 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr19:50881883 C>A maps to NM_007121.4 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:1914103 C>G maps to ENST00000399161 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:32461379 C>A maps to NM_021209.4 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:43919691 C>T maps to NM_172069.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:45801776 G>A maps to NM_018079.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:55615937 C>T maps to ENST00000436346 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:66795860 C>T maps to ENST00000407092 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:71188790 C>T maps to NM_001692.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:85622016 C>T maps to NM_001747.2 *349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:103322366 A>G maps to NM_003048.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:109382667 C>A maps to NM_006267.4 I1891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:109383782 C>G maps to NM_006267.4 S2263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:216177323 C>T maps to NM_004044.6 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:230636273 G>C maps to ENST00000389044 V1896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr2:234079179 G>A maps to ENST00000359570 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr20:32217652 G>A maps to NM_005093.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr20:60900378 G>T maps to NM_005560.3 S1841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr20:61936829 G>C maps to ENST00000326996 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr21:33039669 C>T maps to NM_000454.4 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr21:38463618 G>C maps to NM_003316.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr21:45948428 C>T maps to ENST00000443468 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr22:38609852 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr22:40662820 C>T maps to ENST00000454349 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr22:51019954 G>A maps to NM_005198.4 R159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:9885242 G>C maps to NM_173659.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:38138128 G>A maps to NM_007335.2 V747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:48675651 C>A maps to NM_001407.2 E3309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:69246183 G>C maps to NM_015123.1 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:114070333 C>T maps to NM_001164342.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:137822363 G>T maps to NM_173543.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr3:169654186 C>T maps to NM_182610.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:13708300 G>A maps to NM_001369.2 I4423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:38952312 C>A maps to ENST00000296782 E1038*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:54737721 G>C maps to NM_176895.1 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:98215418 G>C maps to NM_001270.2 S1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:133914844 G>A maps to ENST00000448712 E797E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:134029514 G>A maps to NM_021982.1 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:139941015 C>A maps to ENST00000354402 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr5:140257093 G>A maps to NM_018903.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr6:31382787 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr6:43516010 G>A maps to NM_020750.2 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr6:118588186 G>A maps to NM_001029858.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:2579516 C>G maps to NM_152743.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:30102286 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:45743203 C>G maps to NM_021116.2 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:81346647 C>G maps to NM_000601.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr7:130353956 G>T maps to NM_052933.2 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:75540480 C>G maps to NM_000689.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:91617098 C>T maps to NM_005226.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:131028090 G>A maps to NM_004486.4 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:139326390 G>A maps to NM_019892.3 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chr9:140729269 C>T maps to NM_024757.4 F1254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chrX:49040228 C>A maps to NM_006150.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chrX:119402107 A>G maps to NM_017938.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IT-01A-31D-A20D-08 chrX:151996452 G>A maps to NM_004344.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:1267275 C>T maps to NM_152228.1 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:19454158 G>A maps to ENST00000375267 F3062F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:44072609 C>G maps to NM_002840.3 L1276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:44442264 C>T maps to NM_004047.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:70618117 G>C maps to NM_017768.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:109366067 C>T maps to NM_152763.3 Q697Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:113459917 G>C maps to NM_003051.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:114380650 C>T maps to NM_015967.5 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:118039473 G>A maps to NM_006699.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:144617157 G>T maps to NM_001037675.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:153701121 G>A maps to ENST00000428986 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:154296213 C>T maps to NM_080429.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:156182916 C>T maps to NM_007221.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:158450114 C>T maps to NM_001004472.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:160388961 C>G maps to NM_020335.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:162343918 G>A maps to NM_182581.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:162549314 C>T maps to ENST00000367925 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:171080102 C>T maps to NM_006894.5 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:179989420 A>C maps to NM_014810.4 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:235969822 G>A maps to NM_000081.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:237819280 C>G maps to NM_001035.2 S2709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:241803277 G>A maps to NM_014322.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr1:248616328 C>T maps to NM_001004136.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:3824046 C>G maps to NM_001300.5 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:5791659 C>G maps to NM_017782.4 L2092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:29747178 G>A maps to NM_021738.2 F2214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:30336609 C>T maps to NM_020848.2 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:94733955 G>A maps to NM_019053.4 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:97174256 C>T maps to NM_001034954.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:104678596 C>T maps to NM_017649.3 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:106139899 G>A maps to NM_001008723.1 Q429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr10:135197563 C>T maps to NM_152911.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:17428509 G>T maps to ENST00000302539 I1030I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:46394036 G>A maps to NM_001105540.1 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:57947222 C>T maps to NM_001005212.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:62124475 G>C maps to NM_025080.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:68369378 C>T maps to NM_001164160.1 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:68377462 A>C maps to NM_001164160.1 R854R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:70202352 C>T maps to NM_003626.2 Q859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:110451668 C>T maps to NM_020809.2 K667K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:119228515 C>A maps to NM_004205.4 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr11:122647791 C>T maps to NM_032873.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:21624537 G>A maps to NM_032941.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:21995252 G>A maps to NM_005691.2 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:22627715 G>C maps to ENST00000446597 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:29736356 T>A maps to NM_001193451.1 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:49444683 G>A maps to NM_003482.3 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:53647578 C>T maps to NM_001170790.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:56215781 C>G maps to NM_032364.5 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:83455600 G>A maps to NM_152588.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:97345757 C>G maps to NM_001135175.1 S644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:99640172 G>C maps to NM_152788.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr12:105238267 T>C maps to NM_032148.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr13:26828879 C>T maps to NM_001260.1 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr13:32826016 G>A maps to NM_023037.2 K2391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr13:76335155 C>G maps to ENST00000357063 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:21897299 C>T maps to NM_001170629.1 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:23306100 C>T maps to NM_004995.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:31598385 G>A maps to NM_015382.2 I1397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:64457210 C>G maps to NM_182914.2 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:65220340 C>T maps to ENST00000389723 P2176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:71137850 G>A maps to NM_015351.1 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:79270146 C>G maps to NM_004796.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:94780793 G>A maps to NM_001756.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:96912868 C>T maps to NM_152327.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr14:100795963 C>T maps to NM_207117.2 A303A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:22929847 G>A maps to NM_014608.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:40586547 G>A maps to NM_004573.2 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:41313218 C>T maps to NM_017553.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr15:72455647 C>T maps to NM_001012642.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:2155952 G>A maps to NM_001009944.2 T2592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:30002498 G>A maps to NM_004783.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:31201393 C>A maps to NM_004960.3 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:56388943 C>G maps to NM_020988.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:58576137 C>T maps to NM_016284.3 L1559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr16:67575768 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:4859246 C>T maps to NM_053013.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:11522878 C>G maps to NM_001372.3 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:26958553 G>A maps to NM_014680.2 H1414H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:28296146 A>T maps to NM_198529.3 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:34956405 C>T maps to NM_024308.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:36877000 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:43214492 G>A maps to NM_001135706.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:58313540 G>A maps to NM_032582.3 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:58422943 C>T maps to NM_032582.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:61768565 G>C maps to NM_203351.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:65197254 G>C maps to NM_014877.3 S140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:72285871 C>T maps to NM_023036.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr17:77768459 G>A maps to NM_020649.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:3879140 G>A maps to NM_004746.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:12673396 G>A maps to NM_024899.2 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:14850273 A>T maps to NM_001145029.1 R1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr18:72999152 G>A maps to NM_005786.4 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:3382104 G>A maps to ENST00000269778 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:4428818 C>G maps to NM_005483.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:6270698 G>A maps to NM_005934.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:9025597 A>G maps to NM_024690.2 L12286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:10369341 C>T maps to NM_146387.1 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:11323950 C>T maps to ENST00000319867 L1464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:37441803 G>A maps to NM_198539.2 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:39880313 G>A maps to NM_019088.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:42474361 G>C maps to ENST00000441343 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:46387391 C>T maps to NM_015649.1 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:55672074 C>T maps to ENST00000301249 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:56466275 C>G maps to NM_176811.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr19:57328267 G>A maps to NM_006210.2 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:20138059 G>A maps to NM_001006657.1 Q688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:24345318 C>G maps to NM_199346.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:43968149 C>G maps to NM_172069.3 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:97475113 C>T maps to NM_020184.3 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:101655102 C>T maps to NM_001102426.1 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:160604795 C>G maps to NM_022826.2 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:160698843 G>C maps to NM_001198759.1 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:202073796 C>T maps to NM_032977.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr2:219825384 C>G maps to NM_003936.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:10620147 A>G maps to NM_000214.2 *1219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:46279913 C>T maps to NM_181659.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:50768753 C>T maps to NM_018197.2 Q659Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:62120316 C>A maps to NM_001958.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr20:62896742 C>T maps to NM_018257.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr21:45950979 C>T maps to ENST00000443468 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:25023890 C>A maps to NM_005265.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:37603236 C>T maps to NM_001051.2 W202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:37771106 G>A maps to NM_052906.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:41911841 A>T maps to ENST00000396512 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr22:50318083 G>A maps to NM_001135101.1 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:432753 T>C maps to NM_006614.2 F901F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:14798892 G>A maps to NM_032137.4 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:46712989 G>A maps to NM_147129.3 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:49716345 G>A maps to ENST00000438011 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:52835026 C>T maps to NM_002217.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:98189001 C>T maps to NM_001004736.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:108626913 G>T maps to NM_005459.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:111603862 C>T maps to NM_001134438.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:126208125 G>A maps to NM_001165974.1 F627F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:152880589 C>T maps to NM_002886.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:164724635 G>T maps to NM_001041.3 L1458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr3:179597762 C>T maps to NM_016559.1 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:36212142 C>G maps to NM_015230.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:39254831 G>C maps to NM_025132.3 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:46390672 G>A maps to ENST00000507069 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:46973160 C>T maps to NM_000809.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:69188521 G>A maps to NM_001031732.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:69874574 G>T maps to ENST00000381096 S437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:71339776 G>A maps to NM_152291.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:77691978 C>T maps to NM_020859.3 S1850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:126371441 C>T maps to NM_024582.4 Q3091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr4:155157961 G>T maps to NM_017639.3 V2159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:5239386 C>T maps to NM_139056.2 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:5239992 G>A maps to NM_139056.2 E826E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:34924953 C>T maps to NM_018321.3 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:52355783 C>T maps to NM_002203.3 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:63257012 C>A maps to NM_000524.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:82835571 G>A maps to NM_004385.4 E2250E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:90149229 G>A maps to NM_032119.3 L5778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:112178931 G>A maps to NM_001127510.2 W2547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:141044641 G>A maps to NM_022481.5 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:149375649 C>A maps to NM_030953.2 E88*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DK-A3IU-01A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr5:180048703 G>A maps to NM_182925.4 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:2769088 G>A maps to NM_020135.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:7899901 G>A maps to NM_030810.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:33146476 G>A maps to NM_080680.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:56334712 G>A maps to ENST00000361203 Q7269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:73787120 C>G maps to NM_001160133.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:97613183 C>T maps to NM_198468.2 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:111702566 G>A maps to NM_002912.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:117128366 C>T maps to NM_148963.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:132201158 T>C maps to NM_006208.2 Y695Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr6:160555031 C>T maps to NM_003057.2 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:47898447 G>A maps to NM_138295.3 Y1395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:63538395 G>A maps to NM_001159522.1 W323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:65705933 C>T maps to NM_003596.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:82579160 C>T maps to NM_033026.5 L3581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:99695469 C>G maps to NM_005916.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:100283074 G>A maps to NM_022574.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:100696365 G>A maps to NM_001040105.1 L4401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:103848301 G>A maps to NM_002553.3 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:139826544 G>C maps to NM_030647.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr7:141759284 C>G maps to ENST00000475668 S1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:55533795 C>T maps to NM_006269.1 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:87486537 C>T maps to NM_016033.2 *315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:87486542 C>T maps to NM_016033.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:88885229 C>A maps to NM_152418.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:103564038 C>T maps to NM_024410.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:105509411 G>A maps to NM_013437.4 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:113267561 A>G maps to NM_198123.1 F3319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:133880418 C>T maps to NM_003235.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:133945804 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:139278011 C>G maps to NM_015912.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr8:144940860 G>A maps to NM_031308.1 L2187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr9:27566842 C>T maps to NM_018325.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr9:34635838 G>A maps to NM_005866.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chr9:36276901 G>A maps to NM_001128227.2 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:30872613 G>A maps to NM_152787.3 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:52844215 A>C maps to NM_130775.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:53578271 C>G maps to ENST00000276009 V3019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:101912846 C>T maps to NM_001184727.1 Q1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:102471434 C>T maps to NM_001080425.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:105281022 G>C maps to NM_000354.5 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IU-01A-11D-A20D-08 chrX:142718201 G>T maps to NM_001184749.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:1268917 G>T maps to NM_152228.1 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:47904408 G>A maps to NM_004474.3 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:172410940 A>G maps to NM_153747.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr1:204951128 C>T maps to ENST00000367172 I817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr10:38121104 G>C maps to NM_021045.1 S393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr10:124793888 G>T maps to NM_001609.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr11:85420379 G>C maps to ENST00000359152 S1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr12:11546867 T>C maps to NM_006248.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr12:53007513 G>A maps to NM_175068.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr12:113873340 C>G maps to NM_138432.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr14:19553679 C>T maps to NM_001005356.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr14:47530527 C>T maps to NM_001113498.2 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr17:28380459 G>A maps to NM_198529.3 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr17:47395036 C>T maps to NM_014897.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr17:60028188 A>G maps to NM_005121.2 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:4792856 C>T maps to NM_018708.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:22156620 A>G maps to NM_007153.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:23927145 A>G maps to NM_138286.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:38579388 G>A maps to NM_015073.1 E521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:42931253 T>C maps to NM_005357.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:53209408 G>T maps to NM_001161500.1 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:53644361 C>T maps to NM_001172674.1 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr19:55993618 G>T maps to NM_033113.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr2:80530713 G>A maps to NM_178839.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr2:225651828 G>A maps to NM_014689.2 D1855D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr20:62044921 G>A maps to NM_172107.2 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr22:18210131 G>A maps to NM_015367.2 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr22:23438064 C>T maps to NM_002073.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr3:52552853 C>G maps to NM_015136.2 S1668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr5:59893729 G>A maps to NM_018369.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:27861554 G>A maps to NM_003527.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:30712139 G>A maps to NM_003897.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:50791307 C>T maps to ENST00000263046 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:131490372 G>A maps to ENST00000431975 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr6:167590517 C>T maps to NM_001145121.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3IV-01A-22D-A21A-08 chr9:86571109 C>A maps to NM_032307.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:3348545 G>T maps to NM_022114.3 E1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:8399746 C>T maps to ENST00000377479 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:10479589 C>T maps to NM_002631.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:16073401 G>A maps to NM_001013641.1 Q266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:16382216 G>A maps to NM_000085.3 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:18661422 G>T maps to NM_032880.4 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:21795328 C>G maps to NM_032264.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:22203043 G>A maps to NM_005529.5 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:32828366 C>G maps to NM_052841.3 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:45811225 G>A maps to NM_007170.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:50884474 G>A maps to NM_032110.1 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:59042363 G>A maps to NM_002353.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:62483542 C>T maps to NM_176877.2 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:78269065 C>G maps to NM_198549.2 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:86952366 C>T maps to NM_001285.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:92752070 G>A maps to NM_053274.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:92752142 G>A maps to NM_053274.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:109865576 G>C maps to NM_002959.4 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:111492646 C>T maps to NM_018372.3 K565K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:111734818 G>A maps to NM_024901.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:114189164 C>T maps to NM_001142782.1 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:117078794 G>C maps to NM_001779.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:118535109 C>G maps to NM_206996.2 L1780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:144876028 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:145273376 G>C maps to ENST00000454606 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:147091377 C>T maps to NM_004326.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:150679154 C>G maps to NM_032132.4 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:151378585 C>T maps to NM_015100.3 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:151492648 C>G maps to NM_020770.2 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:152128073 G>A maps to NM_001122965.1 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:154956262 C>G maps to NM_025207.4 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:155001831 G>A maps to NM_144622.2 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156146337 G>A maps to NM_022367.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156146607 C>T maps to NM_022367.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156247730 G>A maps to NM_015327.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156316676 G>A maps to NM_144627.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:156562242 C>T maps to ENST00000446584 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:157776904 G>A maps to NM_052938.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:158061273 C>T maps to ENST00000368173 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:161753802 C>T maps to NM_007348.2 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:167409969 G>T maps to NM_198053.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:176998853 C>A maps to ENST00000281881 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:179526244 G>A maps to NM_014625.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:179526362 G>A maps to NM_014625.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:200377313 G>C maps to NM_012482.3 S507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:200880790 C>T maps to NM_018265.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:206904054 G>A maps to NM_032960.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:206944332 C>T maps to NM_000572.2 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:207651345 G>T maps to NM_001006658.2 E1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:208062849 C>T maps to NM_001025109.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:217784237 G>A maps to NM_018040.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:220752865 C>T maps to NM_018650.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:223536709 G>A maps to NM_017982.3 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:229779296 C>T maps to NM_014777.2 Q1218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:237619913 C>T maps to NM_001035.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr1:243433446 G>A maps to NM_006642.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:27294519 C>G maps to NM_014915.2 *1711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:28032179 G>C maps to NM_173576.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:50374938 C>G maps to ENST00000374148 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:50678884 G>A maps to NM_000124.2 Q1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:51768908 G>T maps to NM_001077665.2 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:64952853 G>A maps to NM_032776.1 Q1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:69902715 G>T maps to NM_032578.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:73437305 G>A maps to ENST00000398860 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:75567555 G>A maps to NM_003635.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:77158842 C>T maps to NM_032772.4 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:88704121 G>A maps to NM_024756.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:98145843 G>A maps to NM_012465.3 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:99123622 C>T maps to NM_015179.3 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:101639648 G>T maps to ENST00000342239 L1513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:103607319 C>A maps to NM_024541.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:126631752 C>T maps to NM_017580.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:129904352 G>A maps to NM_002417.4 I1917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr10:133918365 C>T maps to NM_001105521.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:2929500 C>T maps to NM_002555.5 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:5142388 G>A maps to NM_001005222.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:5530515 G>A maps to NM_017481.2 I91I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:5968680 C>T maps to NM_001003443.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:10483089 G>A maps to NM_000480.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:31648698 G>A maps to ENST00000395934 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:46418999 C>T maps to ENST00000458649 *1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:47073975 C>T maps to NM_001003677.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:47259518 G>A maps to NM_000107.2 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:48161323 C>T maps to NM_002843.3 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:55890711 C>G maps to NM_001005201.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:56086159 C>T maps to NM_001005202.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:57373935 C>T maps to ENST00000403558 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:61058811 G>A maps to NM_152718.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:61672246 G>A maps to NM_013401.2 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:62416060 G>A maps to NM_030628.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:62483064 G>A maps to NM_001079559.1 F690F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:62563951 G>A maps to NM_006362.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:67402489 C>T maps to NM_005995.4 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:76063501 G>C maps to NM_004705.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:78177017 C>T maps to NM_024678.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:93118580 C>G maps to NM_181645.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:108196790 G>T maps to NM_000051.3 E2272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:108547944 C>A maps to NM_004398.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:111888512 G>A maps to NM_001037954.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:113631012 G>C maps to NM_004724.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:117988105 G>A maps to NM_019894.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:123597520 C>T maps to NM_003455.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:126142910 G>A maps to NM_017547.3 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:129744721 G>A maps to NM_006165.3 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr11:134252639 G>A maps to NM_054025.2 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:2224702 C>G maps to NM_199460.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:6933171 C>G maps to NM_019858.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:12022356 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:15068614 G>A maps to NM_152321.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:27553557 G>A maps to NM_020183.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:48962943 G>C maps to NM_002289.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49334842 C>T maps to NM_001659.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49406882 G>C maps to NM_002733.3 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49427437 G>A maps to NM_003482.3 Q3684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49485100 C>T maps to NM_021044.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:49689306 C>T maps to ENST00000451891 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:50035704 C>T maps to NM_001031698.1 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:52865854 C>T maps to NM_173086.4 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:53858605 C>T maps to NM_005016.5 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:56349423 G>C maps to NM_006928.3 S529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:57181044 C>T maps to NM_003725.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:104719162 C>T maps to NM_001093771.1 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:106770205 G>C maps to NM_018082.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:113304638 G>A maps to NM_001143854.1 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:120575012 C>T maps to NM_006836.1 K2258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:123424765 C>T maps to NM_203444.2 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:123889519 C>T maps to NM_020382.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:124293451 C>T maps to NM_207437.3 I914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr12:132502202 G>A maps to ENST00000333577 A1385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr13:58207696 C>G maps to NM_001040429.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr13:99037048 C>T maps to NM_005766.2 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr13:99520265 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:19378097 C>T maps to NM_001013354.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:23524349 G>A maps to NM_022478.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:23865620 G>A maps to NM_002471.3 F767F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:23899053 G>A maps to NM_000257.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:24424330 G>A maps to NM_021004.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:24801005 C>T maps to NM_139247.3 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:24880395 G>A maps to NM_025081.2 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:38679238 C>T maps to NM_001049.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:55852643 G>A maps to NM_014924.3 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:65521358 C>T maps to ENST00000448390 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:68196079 G>C maps to NM_152443.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:69262699 G>A maps to NM_207442.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:70989716 G>A maps to NM_003814.4 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:75513112 C>T maps to NM_001040108.1 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:75514903 C>T maps to NM_001040108.1 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:76045554 G>A maps to NM_017791.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:77493964 C>T maps to NM_024496.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:77706017 C>T maps to NM_020431.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:100405532 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:101005142 G>A maps to NM_020836.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:101005460 G>A maps to NM_020836.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105397101 C>T maps to NM_138790.2 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105410847 G>T maps to NM_138420.2 S3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr14:105415184 G>A maps to NM_138420.2 L2201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:29367149 G>A maps to NM_005503.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:31360133 G>A maps to NM_002420.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:43294804 G>A maps to NM_174916.2 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:50769683 G>A maps to NM_005154.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:59910808 G>A maps to NM_004751.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:59911183 G>A maps to NM_004751.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:60789728 C>T maps to NM_134260.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:65847288 G>A maps to NM_016395.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:68503653 G>A maps to NM_017882.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:68609617 G>A maps to ENST00000423218 F900F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:73624576 G>A maps to NM_005477.2 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:76994203 G>A maps to ENST00000324767 I801I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:78635839 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:81199100 G>A maps to NM_018689.1 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:81660669 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr15:89417255 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:3065462 G>T maps to NM_021195.4 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:3139502 G>A maps to NM_032805.1 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:15718641 G>A maps to NM_014647.3 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:15835628 C>T maps to NM_001040114.1 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:16184357 C>T maps to ENST00000399408 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:17211611 C>T maps to NM_022166.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:23767006 G>A maps to NM_022097.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:27544707 C>T maps to NM_001520.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:28603659 C>T maps to NM_001054.3 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:28883707 C>T maps to NM_001145795.1 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:48162608 G>A maps to NM_033226.2 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:48290642 G>A maps to NM_031490.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:57710247 C>T maps to NM_170776.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:68721568 C>T maps to NM_001793.4 H575H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:71610276 G>C maps to NM_000353.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:71718465 G>A maps to NM_015020.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:72094737 G>A maps to NM_005143.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:72828401 C>A maps to NM_006885.3 E2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:77353979 C>T maps to NM_199355.2 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:81198280 G>A maps to NM_052892.3 L1105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:84215614 C>T maps to NM_005679.2 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:84883008 C>T maps to NM_031476.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:89777027 C>T maps to NM_004913.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr16:90106742 C>T maps to NM_001481.2 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:1478942 G>C maps to ENST00000382147 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:6589553 C>T maps to NM_177550.3 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:7256926 C>G maps to NM_001002914.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:7700819 C>T maps to NM_020877.2 L2684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:8814739 G>A maps to NM_001142633.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:17772712 G>A maps to NM_001082968.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:26697286 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:27579108 C>T maps to NM_005208.4 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:36486037 C>T maps to ENST00000398597 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:36486124 C>T maps to ENST00000398597 E1110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:38859915 G>A maps to NM_019016.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40068699 C>T maps to ENST00000401700 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831708 G>A maps to NM_016602.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831732 G>C maps to NM_016602.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831759 G>A maps to NM_016602.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40831891 G>A maps to NM_016602.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:40864324 C>A maps to ENST00000264646 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:41174208 G>T maps to NM_006373.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:41610075 G>A maps to NM_001079675.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:42289311 G>C maps to NM_014233.2 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:42398043 C>T maps to NM_001143780.1 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:48046846 C>T maps to NM_138281.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:48600298 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:48632591 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:50235294 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:56569024 C>T maps to NM_004687.4 *1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:58128215 G>A maps to NM_022070.4 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:60059865 G>C maps to NM_005121.2 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:61560830 C>T maps to NM_000789.3 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:61601525 C>T maps to NM_030779.2 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:62533746 G>A maps to NM_138363.1 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:63156420 C>G maps to NM_003835.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:66423332 G>A maps to NM_017983.5 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:73725399 C>T maps to NM_001005619.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:76557990 G>C maps to ENST00000389840 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:76831482 G>A maps to NM_025090.3 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:78061847 G>A maps to NM_017950.2 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:78328355 C>G maps to NM_020914.4 L3663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:79918539 C>T maps to NM_178493.5 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:79941447 C>T maps to ENST00000306729 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:79988620 G>A maps to NM_144999.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:80196576 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr17:80789061 C>T maps to NM_024702.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:346721 G>A maps to NM_130386.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:5397425 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:13059090 C>G maps to NM_032142.3 S1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:34415223 C>G maps to NM_020776.1 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:44682581 G>C maps to NM_016097.3 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr18:47581730 G>A maps to NM_001080467.2 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:541368 G>A maps to NM_004359.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:677927 G>A maps to NM_005860.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:677930 C>T maps to NM_005860.2 I81I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:5231462 C>T maps to NM_002850.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:6426468 C>T maps to NM_173637.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:6467704 G>C maps to NM_024898.2 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:6692952 C>T maps to NM_000064.2 V1124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:8381529 C>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:8386541 C>T maps to NM_001031.4 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9059941 G>A maps to NM_024690.2 H9168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9204519 C>G maps to ENST00000305465 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9362192 C>T maps to NM_001079935.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:9639181 G>A maps to NM_024106.1 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:10246919 G>A maps to NM_001130823.1 L1511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:11917626 C>T maps to NM_152356.3 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:12059828 G>C maps to NM_144566.1 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:12800988 G>C maps to ENST00000380339 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:12911748 G>A maps to NM_005809.4 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:13260330 C>G maps to NM_003765.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:15662125 C>T maps to NM_173483.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:18896557 G>A maps to NM_000095.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:20003060 A>T maps to ENST00000427401 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:35517043 G>A maps to NM_020895.3 *725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:36221765 C>G maps to NM_014727.1 S1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:38200663 G>A maps to NM_032689.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:40889767 G>A maps to NM_144685.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:41596469 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:42797159 G>A maps to NM_015125.3 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:42863099 G>A maps to ENST00000251268 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:45781257 G>A maps to NM_031417.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:49656910 G>A maps to NM_002152.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:51452190 G>A maps to NM_012427.4 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr19:57646566 G>A maps to NM_052882.1 Q380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:11586616 C>A maps to NM_198256.2 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:24239768 G>A maps to ENST00000338315 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:27700948 C>T maps to NM_015662.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:39893155 C>G maps to NM_152390.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:46609642 C>T maps to NM_001430.4 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:133539883 C>T maps to NM_207363.2 Q1500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:161052111 G>A maps to NM_000888.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:163360984 G>A maps to NM_033272.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:166020149 C>G maps to NM_006922.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:172803291 C>G maps to NM_003642.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:174131030 C>G maps to NM_016653.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:179478784 G>A maps to NM_133378.4 Q13879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:180348113 G>C maps to NM_152520.4 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:191854375 C>T maps to NM_007315.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:201760083 C>T maps to NM_001136039.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:204354804 C>T maps to ENST00000374493 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:206166206 C>T maps to ENST00000406610 S804S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:207559579 G>C maps to NM_001093730.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:209203276 C>T maps to NM_015040.3 Q1553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:220032962 G>C maps to NM_001144890.1 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:227898174 C>G maps to ENST00000396625 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:232143142 C>A maps to ENST00000359743 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:234621762 C>G maps to NM_019078.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:235404738 G>A maps to ENST00000339728 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr2:242594012 C>G maps to ENST00000337606 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:21492921 G>T maps to NM_002509.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:22562718 G>A maps to NM_021784.4 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:31022244 C>G maps to ENST00000375687 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:33874439 G>C maps to NM_178468.4 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:34065848 G>T maps to NM_007186.3 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:34262519 G>C maps to NM_021100.4 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:44573622 G>C maps to NM_022104.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:44574945 C>T maps to NM_022104.3 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:45130354 C>T maps to NM_018102.3 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:47706099 G>A maps to NM_001316.2 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr20:62275250 G>C maps to NM_015894.2 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:37618603 G>A maps to NM_005128.2 L1442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:37717292 C>T maps to ENST00000290384 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:42845281 C>T maps to NM_001135099.1 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr21:46596308 G>A maps to NM_015833.3 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:41513765 C>T maps to NM_001429.3 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:42463780 G>A maps to NM_000262.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:44342252 G>A maps to NM_025225.2 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:47307989 C>T maps to NM_014346.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:50277807 G>A maps to NM_014838.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr22:50753331 C>G maps to NM_001001794.3 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:9988024 C>T maps to NM_207351.3 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:10382200 G>A maps to NM_001001331.2 I1035I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:13383322 G>A maps to NM_024923.2 I1051I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:21462821 G>A maps to NM_024697.2 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:25773929 C>T maps to NM_018297.3 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:36587729 C>T maps to NM_003149.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:40529227 C>T maps to NM_001145082.2 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:46399401 C>T maps to NM_001123041.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:47868906 C>T maps to NM_138615.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:48884886 G>C maps to NM_004157.2 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:49027928 C>G maps to NM_177938.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:49569107 T>C maps to NM_004393.4 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:49770263 C>G maps to NM_153273.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:52582189 C>T maps to ENST00000296302 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:52621526 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:66433415 G>C maps to NM_015541.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:67049612 C>T maps to NM_032505.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:98109712 G>C maps to NM_001005516.1 L68L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A3WW-01A-22D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:108724085 G>C maps to NM_014429.3 S615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:121207034 C>T maps to ENST00000393672 K1717K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:121547357 C>T maps to NM_001023570.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:123987852 G>A maps to NM_001024660.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:126722264 C>T maps to NM_032242.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:141272698 C>T maps to ENST00000452898 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:141328357 G>A maps to ENST00000452898 K775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:150840607 G>A maps to NM_053002.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:156271469 C>T maps to ENST00000467789 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:179533668 G>A maps to NM_016559.1 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:184043094 C>A maps to NM_001194947.1 I972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr3:190105988 G>A maps to NM_006580.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:265127 C>T maps to ENST00000419098 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:2172899 G>C maps to NM_181808.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:3176446 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:3213723 G>A maps to NM_002111.6 K2161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:10446883 G>A maps to NM_053042.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:25005549 G>A maps to NM_018176.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:25419343 C>T maps to ENST00000510092 R729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:66231706 C>A maps to NM_004439.5 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:68619555 G>T maps to NM_000406.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:78695756 G>A maps to ENST00000512485 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:87023142 C>T maps to NM_138982.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:108820809 C>T maps to NM_152621.5 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:122853554 C>T maps to NM_001130698.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:152096429 G>C maps to NM_001009555.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:153897463 C>T maps to NM_033393.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:154702902 C>T maps to NM_003013.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr4:155180750 G>A maps to NM_017639.3 S1790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:1208933 C>T maps to NM_001003841.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:7773073 G>A maps to NM_020546.2 L748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:32093125 C>G maps to NM_178140.2 S2614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:33937996 C>A maps to NM_016568.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:36953854 C>T maps to NM_133433.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:55206498 C>T maps to NM_139017.4 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:68548243 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:74892359 G>A maps to NM_016218.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:78322342 G>A maps to NM_013391.2 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:79970868 C>T maps to NM_002439.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:94278071 C>G maps to NM_024717.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:130982829 C>G maps to NM_133372.2 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:134060782 G>A maps to NM_021982.1 *1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:134785490 G>A maps to NM_001099221.1 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140166573 C>T maps to NM_018900.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140188376 G>T maps to NM_018907.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140220968 C>G maps to NM_018911.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:140262518 G>A maps to NM_018904.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:145393551 C>T maps to NM_152550.3 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:148206576 C>T maps to NM_000024.5 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:149576665 C>A maps to NM_014228.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:149932878 C>G maps to NM_001543.4 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr5:175772331 G>T maps to ENST00000443967 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:397157 C>T maps to NM_002460.3 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:6152169 G>A maps to NM_000129.3 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:12124514 C>G maps to NM_002114.2 S1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:17781077 G>A maps to NM_022113.4 V1243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:24175046 G>A maps to NM_016356.3 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:26045913 G>A maps to NM_003531.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:27840977 C>A maps to NM_003546.2 *104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:30619213 C>T maps to NM_001161376.1 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:31544354 C>T maps to NM_000594.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:32010103 G>A maps to ENST00000375244 F4082F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:32170229 C>T maps to NM_004557.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:33135225 G>A maps to NM_080680.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:33154505 C>T maps to NM_080680.2 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:33165596 C>T maps to ENST00000374685 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:43415549 C>T maps to NM_033450.2 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:64389976 G>C maps to NM_015153.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:70411791 G>A maps to NM_018368.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:72957811 C>T maps to NM_014989.4 V741V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:76124426 C>A maps to NM_015687.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:82461732 G>A maps to ENST00000369756 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:111136324 G>A maps to NM_015076.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:134350212 G>C maps to NM_145176.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr6:167754886 C>G maps to NM_031949.4 S500*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DK-A3WW-01A-22D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:21640355 G>A maps to NM_003777.3 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:26240220 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:31013634 C>T maps to NM_000823.3 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:31126104 C>T maps to ENST00000409489 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:37298856 G>A maps to NM_014800.9 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:44364972 G>C maps to NM_001220.4 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:48273723 G>A maps to NM_152701.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:99002547 C>T maps to NM_014891.6 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:99453288 T>A maps to NM_022820.3 L249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:99957060 C>T maps to ENST00000413850 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:100245111 C>T maps to NM_016188.4 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:100320677 C>G maps to NM_000799.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:100856158 G>A maps to NM_001084.4 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:111541795 C>T maps to ENST00000428084 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:117431346 G>A maps to NM_033427.2 Q635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:129916529 C>T maps to NM_001869.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:142566062 T>C maps to NM_004445.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:142612711 G>A maps to NM_019841.4 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:148457546 G>T maps to NM_003592.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:148512131 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:148514355 G>A maps to NM_004456.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:150738288 C>A maps to ENST00000297504 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:151802336 G>A maps to NM_022087.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:151859701 G>A maps to ENST00000355193 Q3654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:158456890 C>T maps to NM_017760.5 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr7:158723186 C>T maps to NM_018051.4 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:4851875 C>T maps to NM_033225.5 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:8175696 C>T maps to NM_001080826.1 L1396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:8750289 G>C maps to NM_004225.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:27729501 C>T maps to NM_173833.5 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:30560622 C>T maps to NM_000637.3 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:30969306 C>G maps to NM_000553.4 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:33310998 C>T maps to ENST00000380081 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:36698503 C>G maps to NM_001031836.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:48641545 C>G maps to NM_001080394.1 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:52733176 G>A maps to NM_052937.2 Q270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:55538470 C>T maps to NM_006269.1 R677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:61693579 C>T maps to NM_017780.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:82714734 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:95527161 C>A maps to NM_015496.3 E896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:118847772 C>T maps to NM_000127.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:125555326 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:131073250 C>T maps to NM_018482.2 Q922Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:133740097 G>A maps to ENST00000395406 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:143396399 G>C maps to ENST00000445818 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:145004381 C>A maps to NM_201380.2 E985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr8:145736433 C>T maps to NM_138431.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:2056766 G>C maps to NM_003070.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:16436823 G>C maps to NM_017637.5 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:17464509 G>A maps to NM_017738.2 E1140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:19376563 C>G maps to NM_001010.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:71155604 C>T maps to NM_153237.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:77416816 G>C maps to NM_017662.4 S669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:88247958 G>A maps to ENST00000395847 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:90497817 C>T maps to NM_178828.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:99795231 C>T maps to NM_001333.2 *335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:112153420 C>T maps to NM_002829.3 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:124065294 C>T maps to NM_000177.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:131515055 G>A maps to NM_006336.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:132584878 G>C maps to ENST00000437532 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:136004576 G>C maps to ENST00000393157 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:139906346 G>A maps to ENST00000355090 V1858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:140075250 G>A maps to NM_013366.3 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chr9:140130618 C>T maps to NM_080877.2 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chrX:1499936 C>G maps to NM_002183.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chrX:2406873 G>A maps to NM_004729.3 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chrX:37027544 C>G maps to NM_001013736.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chrX:53222480 G>T maps to NM_004187.3 R1451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WW-01A-22D-A23M-08 chrX:147088241 C>T maps to NM_152578.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:35579713 A>C maps to NM_024772.3 V761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:45475256 C>T maps to NM_024602.5 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:111147110 C>T maps to NM_004974.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr1:230391012 G>A maps to NM_004481.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr11:8947079 C>T maps to NM_020643.2 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr15:42193058 G>A maps to NM_139265.3 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr19:12491948 T>C did not map to a codon.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr19:12491954 A>C did not map to a codon.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr19:30935716 C>T maps to NM_014717.1 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr4:100458839 C>G maps to NM_032149.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr4:104640577 G>A maps to NM_001059.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr6:31854611 C>T maps to ENST00000395728 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr7:20691116 A>G maps to NM_001163941.1 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr7:147092872 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3WX-01A-22D-A22Z-08 chr8:67514655 G>A maps to NM_001080416.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr16:21210984 G>A maps to NM_003460.1 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr20:33879831 G>A maps to NM_178468.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr22:30685447 C>G maps to NM_001037666.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3WY-01A-11D-A22Z-08 chr4:85617302 T>C maps to NM_014991.4 L2907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:11900228 C>T maps to NM_001286.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:12836178 C>T maps to NM_001080830.1 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:18808296 C>T maps to NM_152375.2 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:22157764 G>A maps to NM_005529.5 L3835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:22333439 C>A maps to NM_005747.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:24201128 C>A maps to NM_001841.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:26507028 C>T maps to ENST00000374253 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:28477355 G>A maps to NM_001164721.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:36766617 C>G maps to NM_005119.3 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:36933438 C>T maps to NM_156039.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:38040349 G>T maps to NM_013285.2 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:38040357 C>A maps to NM_013285.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:40149689 C>T maps to NM_016257.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:45140081 G>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:46159474 G>T maps to NM_016486.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:46768813 G>A maps to ENST00000254454 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:51934201 C>T maps to NM_001981.2 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:52941061 C>T maps to NM_001009881.2 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:54348949 C>T did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:54359912 G>A maps to NM_000792.5 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:55266752 C>T maps to NM_001114108.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:59248199 C>T maps to NM_002228.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:74492541 C>T maps to NM_001105659.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:75198987 C>T maps to NM_138467.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:85787135 C>G maps to NM_012137.3 *286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:94496676 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:109103118 C>T maps to NM_001010883.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:109617650 C>A maps to NM_005645.3 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:114454729 C>T maps to NM_022836.3 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:149871750 G>T maps to NM_016074.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:150259020 C>T maps to NM_144697.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:151259813 C>T maps to NM_020832.1 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:152083291 C>A maps to NM_007113.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:154573728 C>T maps to ENST00000292205 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:155294699 G>A maps to NM_001105203.1 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:158746672 G>A maps to NM_001005278.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:160054011 C>T maps to NM_004983.2 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:161138283 C>T maps to NM_001122764.1 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:161140822 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:196797299 G>A maps to NM_002113.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:196883725 G>T maps to NM_006684.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:201030511 G>A maps to NM_000069.2 I1046I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:201035413 C>T maps to NM_000069.2 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:202273725 G>C maps to NM_001017403.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:202278241 G>A maps to NM_001017403.1 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:202283964 G>T maps to NM_001017403.1 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:209964140 A>G maps to NM_006147.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:214826226 C>A maps to NM_016343.3 L2739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:223983916 G>T maps to NM_001031685.2 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:231472147 G>A maps to NM_175876.3 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:236744561 C>T maps to NM_018072.5 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr1:237872848 C>T maps to NM_001035.2 I3404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:46963915 G>A maps to NM_031912.3 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:102045914 G>A maps to NM_173809.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:118425185 G>C maps to ENST00000388884 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr10:122622424 G>A maps to NM_018117.11 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:498608 G>A maps to NM_203389.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:1862394 G>C maps to ENST00000381906 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:2432723 C>A maps to ENST00000452833 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:5221177 G>A maps to NM_001004760.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:36248960 G>T maps to NM_174902.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:48285747 C>G maps to NM_001004726.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:55798343 C>T maps to NM_001001921.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:58391556 G>A maps to NM_000614.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:59132260 G>C maps to NM_001004729.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:62763270 C>T maps to ENST00000430500 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:64033996 C>T maps to NM_000932.2 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66444532 G>A maps to NM_031492.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627176 C>A maps to NM_024036.4 C473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627251 C>A maps to NM_024036.4 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627353 C>G maps to NM_024036.4 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:66627410 C>G maps to NM_024036.4 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:71238671 C>G maps to NM_001012503.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:71726868 C>G maps to ENST00000393695 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:72466775 C>T maps to NM_006645.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:73686630 C>T maps to NM_003355.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:76825377 G>C maps to ENST00000360841 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:94328538 C>G maps to NM_152431.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:102100565 G>C maps to NM_001130145.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:111965690 C>G maps to NM_003002.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118221327 C>T maps to NM_000073.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118369131 C>T maps to NM_001197104.1 L1950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118390357 G>A maps to NM_001197104.1 G3724G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118390448 G>T maps to NM_001197104.1 E3755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118827611 C>G maps to NM_006760.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:118827674 C>T maps to NM_006760.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:121384942 C>G maps to NM_003105.5 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:122848502 C>A maps to NM_001098169.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr11:124933295 C>T maps to NM_198277.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:674517 G>A maps to NM_016533.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:4643349 C>T maps to NM_020374.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:6675397 C>A maps to ENST00000382421 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:9321514 G>C maps to NM_002864.2 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:22697069 C>T maps to ENST00000446597 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:29604324 G>C maps to NM_183378.2 S903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:39751994 G>C maps to ENST00000395670 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:49420240 G>A maps to NM_003482.3 Q5170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:50570906 G>C maps to NM_001113546.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:52882122 A>G maps to NM_005554.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:52913531 G>A maps to NM_000424.3 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:53722169 C>T maps to NM_001173467.1 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:53776784 C>T maps to NM_138473.2 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:53825227 C>T maps to NM_020547.2 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:56618690 G>T maps to NM_024068.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:56715865 C>T maps to NM_001127460.2 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:89996870 G>A maps to ENST00000428670 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:108685926 G>A maps to NM_001142344.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:109577218 G>A maps to NM_001093.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:113348979 G>A maps to NM_001032409.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:124298138 C>A maps to NM_207437.3 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:125270803 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr12:133277848 C>A maps to NM_018663.1 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:22077088 C>G maps to NM_152726.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:32915106 G>T maps to NM_000059.3 V2205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:48947602 C>G maps to NM_000321.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr13:97986586 C>T maps to ENST00000376673 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:20928360 G>T maps to NM_001100814.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:45693437 C>T maps to NM_018353.4 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:50117144 G>T maps to NM_002692.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:72200446 C>T maps to NM_015556.1 P1663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:76045893 C>T maps to NM_017791.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:77712284 C>G maps to NM_020431.2 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:94394795 C>A maps to NM_138344.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:95234905 C>T maps to NM_173849.2 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:96807900 C>T maps to NM_018036.5 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:96944838 G>A maps to NM_152327.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr14:104165272 G>T maps to NM_005432.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:33359340 G>A maps to NM_001103184.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:34649343 C>T maps to ENST00000438749 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:43739642 G>A maps to NM_001141980.1 I919I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:44900790 C>A maps to NM_025137.3 E1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:45424172 C>T maps to NM_175940.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:48720648 C>T maps to NM_000138.4 T2297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:53081807 C>A maps to NM_004498.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:68596208 G>T maps to ENST00000423218 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:70347432 G>T maps to NM_005078.2 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:73409169 C>T maps to NM_002499.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:74749004 G>T maps to NM_201265.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:78386495 C>T maps to NM_001101404.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:80465455 C>T maps to NM_000137.1 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:89867415 C>A maps to NM_002693.2 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:91483661 C>T maps to NM_018671.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:93595351 C>T maps to NM_020211.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr15:99672777 C>T maps to ENST00000336292 R1404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:109025 C>T maps to NM_022450.3 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2012817 G>A maps to NM_002952.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2090034 C>A maps to NM_002528.5 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2237187 C>A maps to NM_020764.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:2286828 C>T maps to NM_001374.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:4933532 G>C maps to NM_002705.4 S1708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:10911961 G>A maps to NM_001079512.2 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:21115864 C>A maps to NM_017539.1 E765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:23119405 G>C maps to NM_020718.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:28331408 G>T maps to NM_001024401.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:29852915 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:30581605 G>C maps to NM_145271.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:30581749 G>T maps to NM_145271.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:30795475 G>C maps to NM_001080417.1 S58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:31235661 C>G maps to NM_001008274.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:48286110 G>A maps to NM_031490.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:57608777 C>T maps to ENST00000349457 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:67265986 A>C maps to NM_013241.2 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:67327462 C>T maps to NM_001100915.1 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:67671649 G>T maps to NM_006565.3 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:69143702 C>T maps to NM_005329.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:69143909 C>G maps to NM_005329.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:70363868 C>T maps to NM_007242.4 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:72174472 C>T maps to NM_031293.2 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:84270992 C>T maps to NM_172347.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:85691039 C>A maps to NM_014615.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:89346346 T>C maps to NM_013275.4 A2201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:89789203 C>T maps to NM_001113525.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr16:89922054 C>T maps to NM_032451.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:5347828 G>C maps to ENST00000457531 S666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:7365510 G>T maps to NM_020899.3 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:7460636 C>A maps to NM_003809.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:18668066 G>T maps to ENST00000395665 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:26818798 C>T maps to NM_001145975.1 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:27943317 G>A maps to ENST00000345068 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:35298105 C>T maps to NM_005568.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:37347814 G>C maps to NM_000723.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:40117263 A>G maps to ENST00000377543 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:40818471 C>G maps to NM_016437.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:41341648 G>A maps to NM_005899.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:42992743 G>C maps to NM_002055.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:43345028 C>T maps to ENST00000344686 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:46973040 C>G maps to NM_005175.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:48750879 C>T maps to NM_003786.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:58288741 G>C maps to NM_032582.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:61787957 G>A maps to NM_001003787.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:66352861 C>A maps to NM_014960.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:68171222 G>T maps to NM_000891.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:73164439 G>C maps to NM_006937.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:78059851 G>A maps to NM_017950.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:79220393 C>T maps to NM_001037984.1 E774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr17:80391556 C>T maps to NM_173620.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:7010381 G>C maps to NM_005559.2 L1230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:7080412 G>A maps to NM_005559.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:70417769 G>C maps to NM_153181.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:70451006 G>A maps to NM_153181.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr18:74091003 G>A maps to ENST00000443185 G1022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:1978736 C>T maps to NM_001319.6 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:2226779 C>G maps to ENST00000221482 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:3284909 G>C maps to NM_021938.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:3979970 C>A maps to NM_001961.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:7083275 G>T maps to NM_024341.2 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:7794774 C>G maps to NM_198492.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:11943308 C>T maps to NM_152357.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:14232406 G>C maps to NM_018154.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:14232457 G>A maps to NM_018154.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:16495954 G>A maps to ENST00000455140 F744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:16528406 C>T maps to ENST00000455140 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:31039180 G>A maps to NM_014717.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:31768676 C>T maps to NM_020856.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:34912526 C>T maps to NM_032346.1 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:34912555 C>T maps to NM_032346.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:36365500 C>T maps to NM_001024807.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:38713254 G>A maps to NM_001135155.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:39963712 C>A maps to NM_003169.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:39963871 C>A maps to NM_003169.3 S763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:40009745 G>A maps to NM_182704.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:40872414 G>T maps to NM_012268.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:41633860 C>A maps to NM_000774.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:41709439 C>T maps to ENST00000301173 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:43026085 C>T maps to NM_001712.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:49132305 C>A maps to NM_020126.3 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:49514295 C>T maps to NM_006666.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:49842009 G>A maps to NM_001774.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:50017148 C>T maps to NM_004107.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:52375789 C>A maps to NM_032679.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:52719906 G>A maps to NM_014225.5 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:54600326 G>A maps to NM_130771.3 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr19:54627902 C>G maps to NM_015629.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:9628346 C>T maps to NM_001039613.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:27589788 G>T maps to NM_172195.3 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:27907999 G>T maps to NM_018158.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:37041502 G>A maps to NM_053276.3 *694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:37410657 C>G did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:38302447 C>T maps to NM_000104.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:44041637 G>A maps to NM_022436.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:69053292 C>G maps to NM_001007231.2 V636V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:73519499 G>A maps to NM_001965.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:74749804 G>C maps to NM_133637.2 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:74763221 G>C maps to NM_032603.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:80530005 C>T maps to NM_178839.4 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:133541788 A>G maps to NM_207363.2 I865I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:166908449 G>C maps to NM_001165963.1 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:170669017 T>C maps to ENST00000442181 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:190428685 G>A maps to NM_014585.5 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:193049158 C>T maps to NM_016192.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:198257806 T>C maps to NM_012433.2 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:233398642 C>G maps to NM_000751.1 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:240958024 G>A maps to ENST00000404554 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:242157736 C>T maps to NM_001001891.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr2:242815143 C>T maps to NM_173821.2 F479F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:10653408 G>A maps to NM_000214.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:20177347 G>T maps to ENST00000389655 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:31021534 C>T maps to ENST00000375687 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:39832520 C>A maps to NM_015035.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:45192107 G>T maps to NM_022829.5 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:48699388 G>A maps to NM_199203.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:57484237 G>A maps to NM_080425.2 V827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:61936862 C>T maps to ENST00000326996 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr20:62200733 G>A maps to NM_001037335.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:33039653 C>G maps to NM_000454.4 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:41496163 G>A maps to NM_001389.3 I1218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:45107623 G>T maps to NM_015056.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr21:47663415 C>T maps to NM_003906.3 L1753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:19506421 C>A maps to NM_001178010.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:19709227 G>T maps to NM_002688.5 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:19839387 G>A maps to NM_024627.5 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:25016335 G>T maps to NM_005265.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:30733034 C>A maps to NM_005877.4 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:36684829 C>A maps to NM_002473.4 R1571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:36894042 C>T maps to NM_001102371.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:38323564 C>G maps to NM_033386.2 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:39425373 G>A maps to NM_152426.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:39477086 C>T maps to NM_021822.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:39710726 C>T maps to NM_000967.3 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:40058010 C>T maps to NM_021096.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:42422776 C>G maps to NM_152613.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:43230282 C>A maps to NM_014570.4 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:43447824 C>T maps to NM_012263.4 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:46655580 A>G maps to NM_006071.1 H1213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr22:50719196 C>T maps to NM_012401.2 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:12877706 C>T maps to ENST00000273223 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:37574871 C>T maps to NM_002207.2 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:38359723 C>G maps to NM_004803.3 S590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:40352531 G>A maps to NM_005875.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:49054899 T>C maps to NM_001009996.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:62188854 G>A maps to NM_002841.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:74351883 C>T maps to NM_020872.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:100432574 C>T maps to NM_001007565.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:100432660 C>T maps to NM_001007565.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:101540510 C>T maps to NM_145037.2 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:101540530 C>T maps to NM_145037.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:123419599 C>T maps to NM_053025.3 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:123634089 G>A maps to NM_022757.4 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:129007758 C>T maps to NM_001006109.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:130287182 C>T maps to NM_001102608.1 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:130799265 G>C did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:161221330 C>T maps to NM_001080440.1 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:183503989 C>T maps to NM_018023.4 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr3:195516054 G>T maps to NM_018406.5 S799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:3465125 G>A maps to ENST00000389653 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:3768989 C>T maps to NM_000683.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:7194755 C>A maps to NM_020777.2 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:8583002 G>A maps to NM_080819.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:38776989 C>G maps to NM_030956.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:47163396 G>A maps to NM_000812.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:65147236 G>A maps to NM_001010874.4 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:77660798 C>A maps to NM_020859.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:83788010 G>A maps to ENST00000505472 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:88036294 G>A maps to NM_001166693.1 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:88394927 C>G maps to NM_004684.4 *665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:153896614 G>A maps to NM_033393.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr4:184605509 G>A maps to NM_021942.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:5462599 G>A maps to NM_015325.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:24535866 T>C maps to NM_006727.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:34867122 G>A maps to NM_144725.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:36141288 G>A maps to NM_001007527.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:132424171 C>T maps to NM_002154.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:132424225 C>G maps to NM_002154.3 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:137622208 G>A maps to NM_001790.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:145442002 G>T maps to NM_152550.3 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:154272067 C>T maps to NM_015465.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:156375435 G>A maps to NM_138379.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr5:169469045 C>T maps to NM_004946.2 V1262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:5999355 C>T maps to NM_016588.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:25811930 G>C maps to NM_005074.3 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:33411121 C>T maps to NM_006772.2 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:42019183 G>A maps to NM_138572.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:56458792 G>A maps to ENST00000361203 L3921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:83839158 C>G maps to NM_015018.2 S758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:157528458 G>T maps to ENST00000367148 E2102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr6:160525707 G>A maps to NM_000876.2 V2356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:16841375 G>C maps to ENST00000223274 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:44119253 G>C maps to NM_013284.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:44561679 C>T maps to NM_013389.2 K933K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:51092922 G>C maps to ENST00000395542 L1299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:87006663 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:91503795 C>T maps to NM_006980.3 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:99332707 G>C maps to ENST00000292414 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:100684882 G>T maps to NM_001040105.1 E3396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:100771917 C>T maps to NM_000602.3 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:111400252 G>A maps to ENST00000428084 F1382F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:127544798 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:128452892 G>A maps to NM_022742.3 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:130138062 C>A maps to NM_002402.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:132937918 C>A maps to NM_021807.3 S21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:143053717 G>C maps to NM_001031690.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:143884108 G>A maps to NM_001003702.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:150649797 G>A maps to NM_000238.2 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:150709516 C>T maps to NM_000603.4 F1021F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr7:155090018 C>T maps to ENST00000344756 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:20110393 C>A maps to NM_021020.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:38370102 G>C maps to NM_207412.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:53062371 G>A maps to NM_014682.2 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:77618761 C>G maps to NM_024721.4 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:91055004 C>T maps to NM_001359.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:100874103 G>T maps to NM_017890.3 R3740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:103341573 G>A maps to NM_015902.4 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:105361097 C>A maps to NM_030788.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:144897386 G>A maps to NM_182706.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:144993917 G>A maps to NM_201380.2 L3494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:145625826 C>T maps to NM_013291.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr8:145729779 G>A maps to NM_005309.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:8484312 G>A maps to NM_002839.3 V1073V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:21974791 G>T maps to NM_001195132.1 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:32421005 C>T maps to NM_002197.2 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:100963835 G>A maps to NM_018421.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:107288605 G>A maps to NM_001001919.1 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:135940562 C>T maps to NM_001807.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:135947124 C>T maps to NM_001807.3 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:136324272 C>T maps to NM_139025.3 Q1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chr9:139090633 C>T maps to NM_014564.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:15591523 G>A maps to NM_021804.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:47307917 C>T maps to NM_153380.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:48340026 C>T maps to NM_012280.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:48933302 G>C maps to ENST00000322995 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:69521859 G>A maps to NM_012310.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:77244135 G>A maps to ENST00000355691 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:83127892 G>A did not map to a codon.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:103359456 G>T maps to NM_001143978.1 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:119387704 G>A maps to NM_001184742.1 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:123179196 C>A maps to NM_001042750.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:125299589 C>A maps to NM_001013628.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:129053375 G>A maps to NM_006649.3 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:147919172 G>A maps to NM_002025.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DK-A3X1-01A-12D-A22Z-08 chrX:155232649 C>T maps to NM_002186.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:1634991 G>A maps to NM_024011.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:19487578 C>T maps to ENST00000375267 Q1746Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:25893368 C>T maps to NM_015627.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:50941243 C>T maps to NM_007051.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:92757088 G>A maps to NM_053274.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:115318965 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:118640298 C>T maps to NM_206996.2 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:154459061 G>T maps to NM_001010846.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:155013955 G>T maps to NM_152494.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:155226173 G>A maps to NM_005698.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:160520799 G>T maps to NM_001184879.1 Y279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:180217471 G>A maps to NM_033343.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:204412706 G>A maps to NM_002646.3 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr1:248028104 G>A maps to NM_015431.3 E205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:37486373 C>A maps to ENST00000374660 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:50872872 T>C maps to NM_020549.4 N676N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:104157317 A>G maps to NM_001077494.1 K179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr10:118305636 G>A maps to NM_000936.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr11:57319863 G>A maps to NM_004223.3 F143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr11:89956186 C>T did not map to a codon.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:9232331 G>C maps to NM_000014.4 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:53670541 G>A maps to NM_012291.4 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:56236138 C>A maps to NM_002429.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr12:124341733 C>T maps to NM_207437.3 D2072D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr14:24029008 C>T maps to NM_003917.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr14:24884980 C>T maps to NM_025081.2 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr14:77273073 G>T maps to NM_015305.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr15:34648799 G>A maps to ENST00000438749 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr15:45814249 C>T maps to NM_013309.4 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr15:85401421 C>T maps to NM_020778.4 L1353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:24802569 C>T maps to NM_014494.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:69199281 T>C maps to NM_032830.2 D562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:74695238 G>A maps to NM_018124.3 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:89357081 G>A maps to NM_013275.4 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr16:89857864 G>C maps to NM_000135.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:1381473 G>A maps to NM_001080779.1 F436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:27065213 G>A maps to NM_178170.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:39116696 C>T maps to NM_213656.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:57754350 T>A maps to NM_004859.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:61949640 G>A maps to NM_020991.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:61950571 C>T maps to NM_020991.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr17:65353673 G>A maps to NM_002816.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr18:29797897 C>T maps to NM_005925.2 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr18:29797899 C>A maps to NM_005925.2 S688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:10883299 A>G maps to NM_001005361.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:44251839 A>G maps to NM_019108.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr19:53384400 C>T maps to NM_207333.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:32626344 T>C maps to NM_016252.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:74432978 C>G maps to NM_006636.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:97533611 G>A maps to NM_017789.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr2:108998922 A>T maps to NM_006588.2 L126L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E5-A2PC-01A-11D-A202-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr20:61467684 G>C maps to NM_001853.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr20:61597891 C>T maps to NM_022082.3 N359N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:37665691 C>T maps to NM_005128.2 I2240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:37665712 C>T maps to NM_005128.2 F2247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:40783686 A>G maps to NM_152505.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr21:45666348 C>T maps to NM_013369.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:39180206 C>T maps to ENST00000301819 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:49459596 A>T maps to NM_000481.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:58111395 T>C maps to NM_001164317.1 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:108407450 A>G maps to NM_014648.3 K1094K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:128852988 C>T maps to ENST00000418265 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr3:191888333 C>A maps to NM_021032.4 G176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr4:110789061 C>A maps to NM_198506.2 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:476427 G>A maps to NM_004174.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:11022942 C>T maps to NM_001332.2 K979K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:140209958 G>A maps to NM_018909.2 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr5:150946089 G>A maps to NM_001447.2 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:3284171 C>A maps to ENST00000436008 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:7230401 G>T maps to NM_001003699.3 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:42625825 T>G maps to NM_015255.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:123319131 C>G maps to NM_001010852.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:144613023 T>C maps to NM_007124.2 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr6:167755013 G>C maps to NM_031949.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr7:100685856 C>G maps to NM_001040105.1 V3720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr7:143701526 T>A maps to NM_001005281.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr8:17739538 G>A maps to NM_201552.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chr8:28378297 G>A maps to NM_017412.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chrX:15509314 C>T maps to NM_003662.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chrX:44969391 C>A maps to NM_021140.2 C1358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chrX:49107795 C>G maps to ENST00000455775 *457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chrX:70784452 C>A maps to NM_181672.2 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E5-A2PC-01A-11D-A202-08 chrX:123182852 A>C did not map to a codon.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:10713995 C>T maps to NM_001079843.1 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:15986518 T>C maps to NM_006511.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:17942674 C>T maps to NM_018125.3 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:33363846 C>G maps to NM_033504.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:33363912 C>T maps to NM_033504.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:117078650 A>T maps to NM_001779.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:156242174 G>A maps to NM_015327.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr1:241951204 C>G maps to NM_144625.4 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr10:28903603 C>T maps to NM_016628.3 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr12:30863383 G>A maps to NM_001002259.1 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr12:109017669 G>T maps to ENST00000228463 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr14:20928870 G>A maps to NM_001100814.1 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr16:68716272 C>T maps to NM_001793.4 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr16:69458657 C>T maps to NM_030579.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr17:51901069 C>T maps to NM_032559.4 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr17:66972296 G>T maps to NM_080283.3 L1585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr18:43534668 C>G maps to NM_020964.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:3959236 G>A maps to NM_001348.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:12780450 G>C did not map to a codon.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:12780827 G>A maps to NM_032332.3 K47K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A3X6-01A-12D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr19:54849824 G>C maps to NM_012276.3 S66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr2:25990543 G>C maps to NM_018263.4 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr2:241514465 G>T maps to NM_018226.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr20:48098780 G>A maps to NM_004975.2 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr21:30380386 G>A maps to NM_016940.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr22:39497956 C>T maps to NM_001166003.1 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:9974313 C>T maps to NM_153461.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:48732709 G>A maps to ENST00000395509 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:129303366 G>C maps to NM_015103.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr3:142681209 G>A maps to NM_198504.2 Y323Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr5:140432012 C>T maps to NM_013340.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:31712334 G>A maps to ENST00000375742 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:74229728 A>G maps to NM_001402.5 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:87967336 C>T maps to NM_015021.1 F1330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr6:158330749 G>C maps to NM_016224.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:70255357 C>T maps to NM_015570.2 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:104730617 G>A maps to NM_182931.2 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:104731736 G>A maps to NM_182931.2 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr7:104731754 G>A maps to NM_182931.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr8:145624216 G>A maps to NM_013291.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3X6-01A-12D-A22Z-08 chr9:131377918 G>A maps to NM_001130438.2 L1719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:152280710 G>T maps to NM_002016.1 A2217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:186014961 C>T maps to NM_031935.2 G2149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:186158667 C>T maps to NM_031935.2 P5522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:192628535 T>C maps to NM_144766.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:237730001 G>A maps to NM_001035.2 W1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr1:248059028 G>A maps to NM_001001957.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr10:16994308 C>T maps to NM_001081.3 Q1645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr10:74034624 G>A maps to NM_019058.2 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:20180779 G>A maps to ENST00000227256 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:57100510 G>A maps to NM_003146.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:65375773 C>T maps to NM_002419.3 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:88583192 G>A maps to NM_001143831.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:103124074 C>G maps to NM_001080463.1 L3375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:113145991 G>A maps to ENST00000316851 K819K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr11:118348797 C>T maps to NM_001197104.1 R1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:5154245 G>A maps to NM_002234.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:6499850 C>T maps to NM_002342.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:8758000 G>A maps to NM_020661.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:122626340 G>A maps to NM_014938.3 K914K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr12:126138269 G>T maps to NM_052907.2 E751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr13:61987072 C>A maps to NM_022843.3 G387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:30100020 C>T maps to NM_002742.2 E533E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:45605268 G>A maps to NM_020937.2 W12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:52474663 C>T maps to NM_007361.3 W1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:58038710 G>A maps to NM_001080455.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr14:70252942 A>G maps to NM_003049.3 Y146Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-E7-A3Y1-01A-11D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:2305695 G>A maps to ENST00000454671 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:18849752 G>A maps to ENST00000389467 R2374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:54319027 A>G maps to NM_024336.2 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:55525776 A>G maps to NM_004530.4 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr16:75665678 C>T maps to NM_001130089.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr17:47874208 G>A maps to NM_007067.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr17:56619288 G>A maps to NM_001038704.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr17:73100104 C>T maps to ENST00000450736 F438F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr18:55103601 C>A maps to NM_004852.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:3905457 G>T maps to NM_033064.4 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:36216718 G>A maps to NM_014727.1 W1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr19:55816211 C>A maps to NM_032430.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:97035168 C>T maps to NM_015341.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:132021607 C>T maps to NM_001083538.1 T860T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr2:238287357 T>C maps to NM_004369.3 P806P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr20:23586271 C>T maps to NM_001008693.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr21:32575280 T>C maps to NM_003253.2 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr3:68802169 C>T did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr3:69168083 C>T maps to NM_198271.3 Q474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr3:113667648 C>G did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr4:175896927 A>T maps to NM_014269.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:126732389 G>A maps to NM_032446.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:131006320 T>C maps to NM_133372.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:140175217 G>A maps to NM_018905.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr5:140725933 G>A maps to NM_018916.3 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:11190346 C>T maps to NM_006403.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:24850032 C>T maps to NM_014722.2 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:26056506 G>A maps to NM_005319.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:31107474 G>A maps to NM_014068.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:31696842 G>A maps to NM_013974.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:74473392 C>G maps to NM_133493.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr6:88376825 A>T maps to NM_181837.2 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr7:106509635 C>T maps to NM_002649.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr7:158528299 C>T did not map to a codon.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr8:143599521 G>A maps to NM_001702.2 P947P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chr9:139399555 G>A maps to NM_017617.3 N1529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chrX:21675186 A>G maps to NM_153270.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E7-A3Y1-01A-11D-A22Z-08 chrX:123196750 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:12371681 T>C maps to NM_015378.2 H2274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:27057987 C>T maps to NM_006015.4 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:34166204 C>T maps to ENST00000373381 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:37947334 C>T maps to NM_025079.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:51912717 T>C maps to NM_001981.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:55331116 C>T maps to NM_014762.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:75036914 C>T maps to NM_001002912.4 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:120436732 C>A maps to NM_021794.2 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr1:249144437 G>A maps to NM_001136036.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr10:16932502 C>G maps to NM_001081.3 V2874V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr10:47087271 C>A maps to NM_005972.4 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr10:100242423 G>A maps to NM_021828.4 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:57135554 C>T maps to NM_002559.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:62288916 G>A maps to NM_001620.1 F4324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:62289516 G>A maps to NM_001620.1 L4124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr11:77911808 C>T maps to NM_020798.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr12:6344474 G>A maps to NM_001769.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr12:106460645 G>A maps to NM_014840.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr12:110230174 G>A maps to NM_021625.4 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr15:51041037 G>A maps to NM_032802.3 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr15:95019958 C>T maps to NM_018349.3 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:57406488 G>A maps to NM_002996.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:64984874 C>T maps to NM_001797.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:67662346 C>A maps to NM_006565.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr16:77759450 C>G maps to NM_001105663.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:1562038 G>A maps to NM_006445.3 F1719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:7721268 G>C maps to NM_020877.2 L3414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:7915608 C>T maps to NM_000180.3 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:62038714 G>A maps to NM_000334.4 C561C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr17:80223619 T>C maps to NM_001893.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:2913062 A>C did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:21083603 C>T maps to NM_013326.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:43668177 G>A maps to NM_001001937.1 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr18:44593393 C>T maps to ENST00000356157 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:843530 C>T maps to NM_002777.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:33355032 G>A maps to NM_014270.4 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:39281454 G>A maps to NM_001042507.3 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:49934670 G>C maps to NM_020309.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:52658462 G>A maps to NM_001102657.1 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr19:53958024 G>A maps to NM_001008401.3 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:96781354 G>A maps to NM_000682.5 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:127447888 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:189931118 T>C maps to NM_000393.3 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:192818460 A>T maps to NM_016192.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr2:234098578 C>T maps to ENST00000359570 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr20:20144788 C>A maps to ENST00000389655 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr21:44274682 G>C maps to NM_018669.4 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr22:20458067 G>A maps to NM_015672.1 F1078F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr3:62484935 T>C maps to ENST00000383709 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr3:108133161 G>C maps to NM_014981.1 S1374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr3:143691455 G>C maps to NM_173552.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:6843913 C>T maps to NM_014743.2 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:8616128 C>T maps to NM_001014447.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:54280808 A>C maps to NM_030917.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr4:55948800 G>A maps to NM_002253.2 Q1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:7895908 C>T maps to NM_024010.2 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:32229904 G>A maps to NM_001040446.1 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:32230144 C>T maps to NM_001040446.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:110462532 C>T maps to NM_139281.2 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:131931308 C>T maps to NM_005732.3 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:134007547 C>T maps to NM_021982.1 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:141008782 C>T maps to NM_003883.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr5:153144152 C>A maps to NM_001114183.1 Y661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:12164327 C>T maps to NM_002114.2 T2597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:31122286 G>A maps to NM_001105564.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:31378386 T>C maps to NM_000247.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:44797553 C>G maps to NM_181356.1 *329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr6:161455435 C>T maps to NM_005922.2 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr7:99264652 G>A maps to NM_000777.3 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr7:150878046 G>A maps to ENST00000422024 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr8:99761531 G>C maps to ENST00000354930 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chr9:139262241 G>A maps to NM_052813.4 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chrX:53459193 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chrX:69670625 C>T maps to ENST00000194900 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chrX:107978479 C>G maps to NM_003604.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B3-01A-12D-A202-08 chrX:154743793 G>T maps to NM_018196.3 S164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:38332194 T>A maps to ENST00000373026 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:64605961 C>T maps to NM_005012.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:166818580 G>A maps to NM_017542.3 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:227307534 C>T maps to ENST00000366766 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr1:235907457 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr10:52569777 C>T maps to NM_138932.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr10:101967089 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr10:115596919 G>A maps to NM_014881.3 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:60695124 C>T maps to NM_017870.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:62416036 C>T maps to NM_030628.1 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:76751659 A>G maps to ENST00000354301 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:108196035 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr11:124620667 G>T maps to NM_014312.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:427452 C>A maps to NM_001042603.1 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:2973566 C>T maps to NM_202002.1 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:56515545 G>A maps to NM_032786.1 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:122758619 C>G maps to ENST00000302528 L1352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr12:133313490 C>T maps to NM_015114.1 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr14:55509990 T>C maps to NM_199421.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr14:94582169 G>A maps to ENST00000448882 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr15:43552709 G>A maps to NM_201631.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr16:24372923 C>T maps to NM_006539.3 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr16:61858916 C>T maps to NM_001796.2 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr17:40815490 C>G maps to NM_016437.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr17:56651578 C>A maps to ENST00000240361 E1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr17:78225190 G>T maps to NM_173626.3 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr18:43796551 G>T maps to NM_145055.3 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr19:50102617 G>A maps to NM_020719.1 S1256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr2:178362474 A>G maps to NM_003659.3 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr2:233409213 C>G maps to NM_005199.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr21:45861675 C>T maps to ENST00000397932 A1546A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr22:39918552 G>A maps to NM_182810.1 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr3:15283749 T>G maps to NM_014296.2 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr3:44776195 C>T maps to NM_145044.2 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr3:194309272 C>G maps to NM_001166305.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr4:146824286 C>A maps to ENST00000508784 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr4:149073666 A>G maps to ENST00000511528 H825H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr5:140214294 C>T maps to NM_018910.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr6:33144975 G>A maps to NM_080680.2 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr6:34826145 G>A maps to NM_017754.3 Q671Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr6:34826514 G>A maps to NM_017754.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr7:938745 C>T maps to NM_006869.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr7:43982599 T>C maps to NM_015983.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr7:47884663 G>A maps to NM_138295.3 L1722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr8:23112845 C>T maps to NM_152272.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr8:26227899 C>T maps to NM_001177591.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chr8:69030876 C>G maps to NM_024870.2 S1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chrX:2928166 G>C maps to NM_001011719.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chrX:44949072 C>T maps to NM_021140.2 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B5-01A-11D-A20D-08 chrX:123200109 C>T maps to NM_001042750.1 Q728*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FD-A3B6-01A-21D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:27124127 G>A maps to NM_017837.2 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:62993830 G>A maps to ENST00000371140 L1309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:114640499 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:118496157 G>A maps to NM_006784.2 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:155291966 C>T maps to NM_001105203.1 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:155791330 G>A maps to ENST00000368331 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:193020926 C>A maps to ENST00000367450 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:203054921 C>A maps to NM_002479.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:203465268 C>T maps to NM_014359.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:204985456 G>A maps to ENST00000367172 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:207087416 G>A maps to NM_005449.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:245865905 T>C maps to NM_018012.3 *2109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr1:248059564 T>G maps to NM_001001957.2 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:71562458 C>T maps to ENST00000356340 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:103783473 G>A maps to NM_024541.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr10:106737175 C>T maps to NM_014978.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:44097104 C>G maps to NM_032592.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:46783564 G>A maps to ENST00000415402 F1402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:63668460 G>T maps to NM_001039469.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:72418280 C>T maps to NM_001040118.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:82560963 G>C maps to NM_199418.2 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:92616452 G>A maps to ENST00000298047 R4277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:101857621 G>T maps to NM_020802.2 E1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:117391941 G>T maps to NM_020693.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:128842724 G>A maps to NM_001142685.1 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr11:133814124 G>A maps to NM_014987.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:43822322 G>A maps to ENST00000389420 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:51319030 G>A maps to NM_014033.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:51319141 G>A maps to NM_014033.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:53579199 G>A maps to NM_001004304.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:56667505 C>T maps to NM_004077.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr12:81503359 C>T maps to NM_024560.2 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr13:48660458 G>A maps to NM_014166.2 Q108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr13:53602985 C>T maps to NM_006418.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr14:24801041 G>T maps to NM_139247.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr15:48052504 A>T maps to NM_153618.1 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr16:53288442 C>T maps to ENST00000219084 R1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr16:67912684 C>G maps to NM_014329.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr16:89351726 G>C maps to NM_013275.4 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:7673954 C>G maps to NM_020877.2 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:16040726 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:27028138 C>T maps to NM_003170.3 Q1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:39253805 G>A maps to NM_031960.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:40315335 C>A maps to NM_012285.2 E832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:40323896 G>A maps to NM_012285.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:57275119 G>A maps to NM_018304.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:73974646 G>A maps to NM_004035.6 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr17:79911121 C>T maps to NM_178493.5 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:5613500 G>T maps to NM_014649.2 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:7965380 C>G maps to NM_025061.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:9086460 G>T maps to NM_024690.2 S1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:9088658 C>T maps to NM_024690.2 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:12829858 G>A maps to NM_001136196.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:14079425 C>T maps to NM_002918.4 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:15794527 C>G maps to NM_023944.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:34983975 G>C maps to ENST00000270288 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:43382063 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:43575869 A>G maps to NM_031246.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:44050096 C>T maps to NM_006297.2 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:51856529 G>A maps to NM_001014763.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr19:53854451 C>G maps to NM_138374.1 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr2:112838675 C>G maps to NM_032824.2 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr2:159481625 C>T maps to NM_003628.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr2:177034234 C>A maps to NM_006898.4 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr20:40748573 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:34951766 C>T maps to NM_017613.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:43222982 C>G maps to NM_022115.3 A1310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr21:43504215 C>T maps to NM_173568.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr22:40140186 G>A maps to NM_152512.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr22:47073090 C>T maps to NM_015124.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:10094120 C>G maps to NM_033084.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:37055999 C>G maps to NM_000249.3 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:64617493 T>C maps to NM_182920.1 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:119222467 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:122437552 C>T maps to NM_017554.2 R1519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:169572605 G>T maps to NM_024727.2 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr3:184298212 C>T maps to NM_004443.3 V732V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:89660242 G>A maps to NM_014883.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:91760119 C>T maps to NM_183049.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:114275327 G>T maps to NM_001148.4 E1852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:122766712 G>A maps to NM_176824.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:153893635 G>A maps to NM_033393.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr4:156638379 C>T maps to NM_001130684.1 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:453800 T>A maps to ENST00000315013 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:9197324 C>T maps to NM_003966.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:140222771 C>T maps to NM_018911.2 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr5:154395260 G>A maps to NM_001099293.1 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:10404841 G>A maps to ENST00000379613 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:131190960 C>T maps to NM_001431.3 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:132860330 T>A maps to NM_175057.3 Y301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr6:159653693 C>G maps to NM_032532.2 S717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:6730880 G>C maps to ENST00000330442 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:21723452 G>T maps to NM_003777.3 E1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:44734096 C>T maps to ENST00000444676 I545I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:48004978 G>A maps to NM_004507.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr7:94053673 G>A maps to NM_000089.3 Q864Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr8:144991922 G>T maps to NM_201380.2 L4159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr8:145736007 G>T maps to NM_138431.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr9:1057267 C>T maps to NM_181872.4 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr9:27950350 G>A maps to NM_152570.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chr9:79898508 C>T maps to ENST00000376646 N1094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chrX:38019288 G>A maps to NM_006307.4 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chrX:55514286 C>G maps to NM_201286.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B6-01A-21D-A20D-08 chrX:153631495 G>A maps to NM_001009934.1 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr1:16260825 G>C maps to NM_015001.2 V2697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr1:173916584 T>A maps to NM_172071.2 K887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr12:57009071 G>C maps to NM_013449.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr13:49039214 A>T maps to NM_000321.2 K765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr15:40627565 G>A maps to NM_207380.2 H466H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr15:49423005 G>A maps to NM_001143887.1 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr15:73616165 C>A maps to NM_005477.2 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr16:88952448 G>A maps to NM_005187.5 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:7077347 C>T maps to NM_001671.3 W211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:33521025 G>A maps to NM_152462.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:52981123 C>A maps to NM_005486.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr17:72954436 G>A maps to NM_030630.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr19:55690385 C>A maps to NM_003180.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr2:219892614 G>A maps to NM_194302.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr21:37781086 A>C maps to NM_005441.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr21:47588240 C>T maps to NM_001142854.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr22:50688080 G>C maps to NM_032019.5 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr3:42777324 C>T maps to NM_144719.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr3:169502468 A>T maps to NM_018657.4 K515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr3:178919315 G>C maps to NM_006218.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr5:148753932 C>G maps to NM_014443.2 *181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr6:26107883 A>G maps to NM_005323.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr8:38373958 C>T maps to NM_207412.1 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr8:38374030 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chr8:53573711 G>A maps to NM_014781.4 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B7-01A-31D-A20D-08 chrX:139866363 A>G maps to NM_004065.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr11:62407193 C>G maps to NM_198335.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr12:100476854 G>C maps to NM_015054.1 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr17:59560438 G>A maps to ENST00000393853 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr19:39226177 G>T maps to NM_144691.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr2:179474564 C>T maps to NM_133378.4 K14627K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr22:41545869 C>T maps to NM_001429.3 Q829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr3:175293968 A>G maps to NM_207015.2 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:13844960 G>C maps to NM_001369.2 V1752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:33588859 C>T maps to NM_030955.2 E903E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:79974806 C>G maps to NM_002439.3 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr5:180668593 C>G maps to NM_006098.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr6:35426084 G>T maps to NM_021922.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr7:129945684 G>A maps to NM_016352.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr7:149425659 C>G maps to NM_032534.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chr9:107267010 C>G maps to NM_001004485.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3B8-01A-31D-A20D-08 chrX:77372876 C>T maps to NM_000291.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:3697774 G>A maps to NM_020710.2 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:36235552 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:36367598 C>A maps to NM_012199.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:47110886 A>G maps to NM_022745.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:52442690 A>C maps to NM_002867.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:78050333 C>T maps to NM_015534.4 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:101362197 G>A maps to NM_133496.4 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:109731741 G>A maps to NM_020775.3 W425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:114512679 G>A maps to ENST00000426820 L1029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:150444195 G>T maps to NM_015203.3 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:176133010 A>G maps to NM_022457.5 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:186280666 G>A maps to NM_005807.3 V1244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:202569524 C>T maps to NM_177402.4 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:202935954 C>T maps to NM_016243.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:204587881 G>A maps to NM_201630.1 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:213032441 C>T maps to NM_014053.2 F216F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr1:227259909 C>T maps to ENST00000366766 K942K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:3162098 C>T maps to NM_002627.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:7621947 C>A maps to ENST00000256861 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:13655787 T>C maps to NM_003675.3 Y209Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:44112555 G>A maps to NM_145312.3 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:64911925 C>G maps to NM_030759.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:75634269 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:96025624 C>T maps to ENST00000371380 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr10:129903241 G>A maps to NM_002417.4 Q2288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:3026646 C>T maps to NM_001014437.2 V722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:6652343 T>A maps to NM_003737.2 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:64085713 G>A maps to NM_012094.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:64480979 C>A maps to NM_015080.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:65547231 T>A maps to NM_138368.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:66114947 C>G maps to NM_006876.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:68207302 G>T maps to NM_002335.2 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr11:118368670 T>G maps to NM_001197104.1 Y1895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:994163 C>T maps to NM_001184985.1 L1658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:8245361 C>G maps to NM_015509.3 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:44917076 A>G maps to NM_001145107.1 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:49488196 G>A maps to NM_021044.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:57598265 C>T maps to NM_002332.2 G3675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:62785201 G>A maps to ENST00000280377 R742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:65514280 A>G maps to NM_007191.4 H68H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:103246693 G>A maps to NM_000277.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:108912879 A>G maps to NM_007076.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr12:121947734 C>A maps to ENST00000377071 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr13:47409472 G>A maps to NM_000621.3 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr13:49050845 A>T maps to NM_000321.2 K844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr13:107145642 C>T maps to NM_004093.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:21834656 G>T maps to NM_007192.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:24518020 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:36277975 C>T maps to NM_194301.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:65203598 C>G maps to ENST00000394691 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:68233023 G>A maps to NM_015346.3 D1977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:73964941 G>T maps to ENST00000334988 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:92555134 C>G maps to ENST00000359819 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:99723961 C>T maps to NM_138576.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr14:102605681 C>T maps to NM_001017963.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr15:52534273 C>A maps to NM_018728.3 G843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr15:59548520 G>A maps to NM_004998.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr15:80872757 A>G maps to NM_014862.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:3119251 C>T maps to ENST00000416912 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:57719644 C>T maps to NM_170776.4 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:57786830 T>C maps to NM_005886.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:58538109 C>T maps to NM_001130487.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:71571353 G>A maps to NM_001166395.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr16:71706187 C>A maps to NM_015020.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:39923801 G>A maps to NM_021991.2 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:55195740 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:73569201 C>T maps to NM_001031803.1 A856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:74283885 G>A maps to NM_032134.1 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:74737128 C>G maps to NM_024311.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr17:79580441 G>A maps to NM_017921.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr18:20581687 A>G maps to ENST00000360790 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr18:21485587 G>T maps to ENST00000416669 E2242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr18:25532200 A>C maps to NM_001792.3 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:1462113 C>T maps to NM_005883.2 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:1785275 G>C maps to NM_138813.2 Y1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:12298626 T>C maps to NM_003437.3 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:41808693 C>T maps to NM_007040.3 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:42402701 C>G maps to NM_199002.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:47844238 G>T maps to NM_018485.1 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:47879303 C>T maps to NM_014681.5 Q811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:49238542 G>A maps to NM_017805.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:49316712 C>T maps to NM_016246.2 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:50315534 T>C maps to NM_025129.4 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr19:53311302 G>T maps to NM_006969.3 Y33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:275175 C>T maps to NM_004300.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:65248204 C>T maps to NM_003038.4 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:74762467 G>C maps to NM_032603.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:133540951 A>G maps to NM_207363.2 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:153575446 G>A maps to NM_152522.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:179472308 A>C maps to NM_133378.4 P15134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:187533613 T>C maps to NM_002210.3 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:192194755 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:202593267 G>A maps to NM_020919.3 F936F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:202899543 G>C maps to NM_003507.1 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:233322745 C>T maps to NM_001631.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr2:234460030 A>G maps to NM_018218.2 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:13856713 G>C maps to NM_025229.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:31688260 A>G maps to NM_182519.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:33735052 G>A maps to NM_018217.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:40049604 T>A maps to NM_032221.3 V1890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr20:60581775 G>A maps to NM_003185.3 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr21:35497669 G>A maps to NM_032476.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr21:45656810 C>A maps to ENST00000400379 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:5229969 C>T maps to NM_014674.2 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:47484414 T>C maps to NM_012235.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:130381084 C>G maps to NM_001102608.1 G2145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:148889890 C>G maps to NM_032383.3 S966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:195453216 C>G maps to ENST00000447234 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr3:195512567 T>C maps to NM_018406.5 V1961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:3449358 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:15626987 A>C maps to NM_012161.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:54232000 C>A maps to NM_152540.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr4:162697122 G>A maps to NM_020116.3 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr5:32089374 G>T maps to NM_178140.2 E1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr5:35779430 T>G maps to NM_024867.3 L1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr5:40972586 G>C maps to NM_000587.2 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:27101227 G>A maps to NM_021064.4 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:31239078 G>A maps to ENST00000383329 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:33623612 T>C maps to ENST00000374316 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:36483156 G>A maps to NM_007271.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:43156451 A>C maps to ENST00000354495 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:43571700 C>T maps to NM_006502.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:82936932 T>G maps to NM_015525.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:90422325 G>A maps to NM_014611.1 N2466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:91254346 A>C maps to NM_145331.1 Y405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:107011685 T>G maps to NM_001624.2 S1654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr6:154762423 A>C did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:6086640 T>C maps to NM_014413.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:16834566 T>C maps to ENST00000223274 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:43436488 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:120381637 T>C maps to NM_012281.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr7:148769266 G>A maps to NM_152411.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr8:16859520 G>A maps to NM_019851.2 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr8:114290866 G>C maps to NM_198123.1 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:79635343 G>A maps to NM_001013735.1 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:117846584 G>T maps to NM_002160.2 I678I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:140083593 G>A maps to NM_003731.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chr9:140508608 C>G maps to NM_152285.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chrX:14863347 C>A maps to NM_152633.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3N5-01A-11D-A21A-08 chrX:44922669 A>T maps to NM_021140.2 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:21329219 G>A maps to NM_001198801.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:33236197 C>G maps to NM_020888.2 S473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:155449221 G>A maps to ENST00000368346 Q1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr1:175066814 G>A maps to NM_022093.1 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:14839735 G>A maps to NM_000922.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:61978050 G>A maps to NM_002407.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:89885587 G>A maps to NM_005467.3 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr11:134180463 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr12:52574697 G>A maps to NM_182507.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr12:52574707 G>A maps to NM_182507.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr12:55523875 C>T maps to NM_001005243.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr15:64446166 C>T maps to NM_024798.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr15:65316098 C>T maps to NM_139242.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr15:80465389 C>T maps to NM_000137.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr16:69776285 C>T maps to NM_014062.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr16:70190727 C>T maps to NM_017990.3 F862F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:40705229 G>A maps to NM_000413.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:44626215 C>T maps to NM_001006607.2 F1237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr17:73231252 C>G maps to NM_024844.3 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr19:5244215 G>A maps to NM_002850.3 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr19:22271464 C>T maps to NM_033468.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr20:259902 G>A maps to NM_153269.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr20:37357146 C>T maps to NM_080552.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr22:29957497 G>C maps to NM_003634.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr22:30682065 C>T maps to ENST00000434291 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr22:50356726 C>G maps to NM_001001852.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:10401789 G>C maps to NM_001001331.2 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:50220146 C>T maps to NM_004186.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:122123147 G>A maps to NM_014367.3 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:151161337 C>G maps to NM_178822.4 V1799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr3:188933082 G>A maps to NM_198485.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:25664187 A>G maps to NM_006424.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:79462136 G>A maps to NM_025074.6 V3966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:104082408 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126238819 C>T maps to NM_024582.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126238825 C>T maps to NM_024582.4 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126239281 C>G maps to NM_024582.4 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126239577 C>G maps to NM_024582.4 S671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126239779 C>A maps to NM_024582.4 V738V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126240343 C>A maps to NM_024582.4 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126240562 C>G maps to NM_024582.4 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:126241102 C>G maps to NM_024582.4 V1179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr4:183710448 C>T maps to NM_001080477.1 T1836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr5:133942732 C>G maps to NM_016103.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr6:46657988 G>A maps to NM_001010870.2 Q708Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr6:108984896 G>A maps to NM_001455.3 Q287Q. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FD-A3NA-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr6:116442381 C>T maps to ENST00000430695 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr7:45015118 C>T maps to NM_033054.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr7:103202300 C>T maps to ENST00000428762 W1770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr7:148801423 G>A maps to NM_001001661.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:42183486 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:113241089 G>T maps to NM_198123.1 S3620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:120620214 T>C maps to NM_006209.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr8:144803788 G>T maps to NM_139021.2 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chr9:4574008 G>C maps to NM_004170.5 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3NA-01A-11D-A21A-08 chrX:49071569 G>C maps to NM_005183.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:6529487 C>T maps to NM_198681.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:8385896 G>T maps to ENST00000377479 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:24124666 C>T maps to NM_001008216.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:28208581 G>A maps to NM_001105556.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:41282935 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:48701485 C>T maps to NM_001135181.1 F434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:52861994 C>T maps to NM_004153.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:110882502 C>G maps to NM_022768.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:151491798 G>A maps to NM_020770.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:154471659 G>A maps to NM_001010846.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:157650525 C>T maps to NM_052939.3 Q664Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:161094072 G>A maps to ENST00000368005 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:176564282 G>T maps to NM_020318.2 G515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:176659423 A>G maps to NM_020318.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr1:202702684 T>A maps to ENST00000367264 A1287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:16990555 G>A maps to NM_001081.3 S1710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:43088095 G>A maps to NM_006955.1 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:61028375 G>A maps to ENST00000442566 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:91099692 G>A maps to NM_001549.4 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:103649228 A>G maps to NM_024541.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:116732025 C>T maps to NM_139169.4 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:122626259 C>A maps to NM_018117.11 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr10:124708191 C>T maps to NM_024942.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:27405923 C>G maps to NM_018490.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:30032650 C>G maps to NM_002233.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:36512194 C>T maps to NM_145803.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:55735792 G>A maps to NM_001005491.1 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:66190263 G>T maps to NM_178864.3 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:66191515 T>C maps to NM_178864.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:73067779 G>A maps to NM_014786.3 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr11:124440752 C>T maps to NM_001005194.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:41421761 G>T maps to NM_001843.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:52910467 G>A maps to NM_000424.3 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:106712229 A>G maps to NM_152772.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:113554885 C>T maps to NM_001193520.1 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr12:114823366 C>T maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr13:41766514 G>A maps to NM_032138.4 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr14:20586059 C>T maps to NM_001004715.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr15:24921967 C>G maps to NM_018958.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr15:93563488 G>A maps to ENST00000309818 R1718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:1129227 C>T maps to NM_001053.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:11850212 C>T maps to NM_014153.3 E814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:21211120 C>T maps to NM_003460.1 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr16:68021778 C>T maps to NM_022355.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:10216602 A>T maps to NM_003802.2 Y1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:34864916 C>A maps to NM_001163735.1 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:73738529 C>G maps to NM_001005619.1 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr17:78321833 C>T maps to NM_020914.4 V3282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:17426804 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:36278139 G>A maps to ENST00000007510 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:58491153 G>A maps to NM_025027.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr19:58862856 G>A maps to NM_130786.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:68408095 C>G maps to ENST00000409752 *190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:121744053 G>A maps to NM_005270.4 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:128036774 T>C maps to NM_000122.1 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:128408389 G>A maps to NM_005291.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:220326631 C>G maps to NM_005876.4 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr2:238303320 A>C maps to NM_004369.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr20:33147572 C>T maps to NM_181509.1 F83F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FD-A3SJ-01A-12D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr20:35547850 T>C maps to NM_015474.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr21:45746743 G>A maps to NM_002626.4 *781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr22:41077322 C>T maps to NM_005297.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:38743600 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:100992517 G>A maps to NM_016247.2 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:128979194 C>T maps to NM_016128.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr3:147128321 C>G maps to NM_003412.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr4:37687843 C>T maps to NM_001085399.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr4:71500194 G>A maps to NM_031889.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr5:887496 T>A maps to NM_001009877.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr5:154396082 G>T maps to NM_001099293.1 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr5:176863485 C>T maps to NM_002082.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr6:33235698 C>G maps to NM_022553.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr6:56464868 C>A maps to ENST00000361203 E3687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:84628905 G>A maps to NM_152754.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:94989395 G>A maps to NM_000940.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:97862207 G>A maps to ENST00000379795 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:140255468 C>G maps to NM_015689.3 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:149421875 C>G maps to NM_032534.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr7:151902228 G>C maps to ENST00000355193 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:56986682 C>T maps to NM_001146227.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:57354058 G>A maps to NM_001135690.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:72211938 T>A maps to NM_000503.4 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:75156997 C>T maps to NM_020647.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:98943550 G>C maps to ENST00000254898 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:139691859 C>T maps to NM_152888.1 K1024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:145154090 G>A maps to NM_030974.3 Q314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr8:146068515 C>G maps to ENST00000446747 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr9:4118289 T>C maps to NM_001042413.1 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chr9:79441571 C>G maps to NM_015225.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chrX:55050274 G>A maps to NM_000032.4 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SJ-01A-12D-A22Z-08 chrX:70811991 C>G maps to NM_052957.4 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:8927304 C>T maps to NM_001428.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:27094373 C>T maps to NM_006015.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:38161615 G>A maps to NM_018101.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:44423126 C>T maps to NM_014652.3 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:92181852 G>A maps to NM_003243.4 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:167339438 T>G maps to NM_002697.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:169696571 A>C maps to NM_000450.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:186022985 C>A maps to NM_031935.2 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr1:200569536 T>A maps to NM_014875.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr10:82036335 G>T maps to NM_000429.2 Y188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr10:99529458 G>A maps to NM_003015.3 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr10:119043390 G>C maps to NM_173791.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr11:6866954 C>T maps to ENST00000379831 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr11:108122623 A>G maps to NM_000051.3 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr11:122928486 G>A maps to NM_006597.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:49334729 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:51442968 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:52642495 T>G maps to NM_005556.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:57556104 G>T maps to NM_002332.2 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:110783085 G>C maps to NM_170665.3 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:111953956 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr12:123355587 G>A maps to NM_024667.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr13:99020426 C>T maps to NM_005766.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:23346424 G>T maps to NM_014045.3 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:30098273 T>C maps to NM_002742.2 V566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:32031320 C>T maps to NM_025152.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:89069336 C>G maps to NM_024824.4 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr14:91700959 G>A maps to ENST00000238699 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr15:34628776 G>A maps to NM_133647.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr15:62182380 G>A maps to NM_020821.2 S3108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr15:101813018 C>T maps to NM_018445.4 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr16:4511812 C>A maps to NM_020677.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr16:67197578 C>T maps to NM_018378.2 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:3194929 C>G maps to ENST00000397187 *322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:7577078 C>A maps to NM_001126112.1 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:18181484 G>A maps to NM_004618.3 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:37427046 A>T did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr17:64299004 G>A maps to NM_002737.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr18:30350173 C>T maps to NM_020805.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:1475147 G>T maps to ENST00000427685 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:14000222 C>G maps to ENST00000454313 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:32930032 A>G maps to NM_001172774.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:37045698 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:45767972 G>A maps to NM_031417.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:45895488 G>A maps to NM_001142502.1 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:49971708 C>T maps to NM_153329.3 D670D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr19:54483175 C>G maps to NM_031895.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr2:74776494 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr2:98341691 G>A maps to NM_001079.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr2:241661250 G>A maps to ENST00000373308 H1580H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr20:4854732 G>A maps to NM_203327.1 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr20:47248882 C>G maps to NM_020820.3 A1486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr21:47330883 C>T maps to NM_020528.2 I180I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FD-A3SL-01A-21D-A22Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr3:122399789 G>T maps to NM_017554.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr3:186793483 C>T maps to NM_003032.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr4:156136029 C>T maps to NM_000910.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:6750552 C>T maps to NM_006999.4 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:121786477 C>T maps to ENST00000379533 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:134143531 A>C maps to ENST00000452510 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:140249820 C>G maps to NM_018902.3 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:150660725 C>T maps to NM_001145017.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:156714071 G>T maps to ENST00000442283 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr5:161128776 T>A maps to NM_000811.2 *454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:32138225 G>A maps to NM_032741.4 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:83848596 T>A maps to NM_015018.2 S1612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr6:121577356 G>C maps to ENST00000275159 S603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:6862991 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:72883943 G>A maps to NM_032408.3 F923F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:92732104 A>G maps to NM_017654.3 A1102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:128484780 A>T maps to NM_001458.4 K1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr7:129663416 G>C maps to NM_016478.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:34971555 C>T maps to NM_015297.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:37486691 T>G maps to ENST00000377792 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:69423626 T>C maps to NM_001098805.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chr9:137804954 C>T maps to NM_002003.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chrX:109416576 C>A maps to NM_032227.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chrX:123040976 G>A maps to NM_001167.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SL-01A-21D-A22Z-08 chrX:142718329 G>A maps to NM_001184749.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:6639331 C>T maps to NM_138697.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:6639337 C>T maps to NM_138697.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:11561855 G>A maps to NM_020780.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:112308377 G>C maps to NM_007204.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:204125341 G>A maps to NM_000537.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr1:228556047 C>T maps to NM_001098623.1 V6566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:26558050 G>T maps to NM_001134366.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:28196615 G>C maps to NM_018076.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:61835133 T>A maps to NM_020987.2 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr10:115610375 G>C maps to NM_014881.3 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:376346 G>A maps to NM_178537.4 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:5142583 A>T maps to NM_001005222.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:46398101 C>T maps to NM_001105540.1 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:64033996 C>T maps to NM_000932.2 I1129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:65831158 C>G maps to NM_006842.2 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:67353984 C>G maps to NM_000852.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:67353994 C>T maps to NM_000852.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:72292402 G>A maps to NM_002599.3 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr11:123886664 G>A maps to NM_001004462.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:29498395 G>A maps to NM_016570.2 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:30802106 G>A maps to NM_006390.3 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:49427125 G>A maps to NM_003482.3 Q3788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr12:81111213 C>G maps to NM_005593.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr13:110435361 C>T maps to NM_003749.2 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr14:75017810 G>A maps to NM_000428.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:65032528 A>G maps to NM_001797.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:70934908 C>A maps to NM_032821.2 E3015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:89779124 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:89845228 C>T maps to NM_000135.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr16:89858461 C>T maps to NM_000135.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:6979313 G>A maps to NM_182906.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:6980294 G>A maps to NM_182906.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:34079686 C>T maps to NM_139285.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:65104786 G>A maps to NM_014877.3 F1515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr17:73491425 C>T maps to ENST00000375248 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr18:13068355 A>G did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr18:47379926 C>T maps to NM_001080467.2 E1371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:10689594 G>C maps to ENST00000453102 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:11168976 C>T maps to NM_001128849.1 R1523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:18650528 C>T maps to NM_012181.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:19136462 G>A maps to NM_001017392.3 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:20118010 C>A maps to NM_033196.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:48204666 C>T maps to NM_015711.3 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr19:51329141 G>A maps to NM_017509.2 D227D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:24930607 G>T maps to NM_003743.4 E757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:27884011 C>T maps to NM_014860.1 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:30965215 G>A maps to ENST00000295055 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:95766233 T>A maps to NM_031902.3 K306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr2:136562345 G>T maps to NM_002299.2 I1485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:43723921 G>A maps to NM_002251.3 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:55088465 G>A maps to ENST00000357348 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:55206427 G>A maps to NM_003222.3 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr20:60794804 G>C maps to ENST00000317393 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr22:50470354 G>A maps to NM_001080447.1 H489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr22:50717350 C>T maps to NM_012401.2 K1493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:48622543 G>A maps to NM_000094.3 F1300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:57543221 G>A maps to NM_177966.5 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:122598122 C>T maps to NM_032839.2 F445F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr3:183368536 C>T maps to NM_017644.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr5:79797731 G>C maps to NM_205548.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:27805963 G>A maps to NM_003510.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:34824634 C>T maps to NM_017754.3 Q454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:90402856 G>A maps to NM_014611.1 Q3298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr6:100896128 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr7:4830401 C>T maps to ENST00000450194 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr7:99367795 C>T maps to NM_017460.3 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:39044507 C>T maps to NM_145004.5 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:82626197 C>T maps to NM_024699.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:95392432 G>T maps to NM_012415.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:95392460 G>C maps to NM_012415.2 S720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr8:113529419 G>A maps to NM_198123.1 V1533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr9:130482602 G>T maps to NM_144965.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chr9:135781235 C>A maps to NM_000368.4 E577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SM-01A-11D-A22Z-08 chrX:123176494 G>A maps to NM_001042750.1 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:1563942 G>A maps to NM_080875.2 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:15959932 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:16358725 G>A maps to NM_004070.3 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:26153216 G>A maps to NM_001099626.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:33988999 A>G maps to ENST00000373381 D3432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:35657034 G>A maps to NM_005066.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:70736617 T>C maps to NM_030816.4 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:89654465 C>T maps to NM_052941.4 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:93812390 G>A maps to NM_001938.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:109805872 C>T maps to NM_001408.2 G1606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:113456584 A>C maps to NM_003051.3 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:114246789 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:117944918 G>A maps to NM_006699.3 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:119456780 G>A maps to ENST00000369429 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:144917917 G>A maps to NM_014644.4 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:152084108 G>A maps to NM_007113.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:165532805 G>A maps to NM_001005214.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:173953688 C>T maps to NM_172071.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr1:244218533 G>A maps to NM_205768.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:25312421 C>A maps to NM_024838.4 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:30316004 A>G maps to NM_020848.2 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:74899247 G>A maps to NM_001135752.1 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:85984110 C>T maps to NM_001017924.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:103868830 C>T maps to NM_001113407.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:103869735 C>T maps to NM_001113407.1 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:116307491 C>T maps to ENST00000277895 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:124739929 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr10:127486690 G>A maps to NM_000375.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:33308755 C>T maps to NM_005734.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:35492233 G>A maps to NM_015430.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:64119603 C>G maps to NM_032251.5 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:70349009 G>A maps to ENST00000338508 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:71152463 G>A maps to NM_001360.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:108277654 A>G maps to NM_152587.3 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:111853157 G>A maps to NM_001037954.2 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:128709868 G>A maps to NM_000220.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr11:130066284 G>T maps to NM_021978.3 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:6161923 C>T maps to NM_000552.3 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:7254566 G>A maps to NM_016546.2 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:29639198 T>G maps to NM_183378.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:30881857 C>T maps to NM_001002259.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:46244138 C>T maps to NM_152641.2 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:50036433 C>T maps to NM_001031698.1 F676F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:53607866 G>C maps to NM_000966.4 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:54576209 G>C maps to NM_014311.1 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:56637605 C>T maps to NM_173595.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:100452765 C>T maps to NM_015054.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:109530579 G>A maps to NM_001145375.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr12:113515256 C>T maps to NM_004416.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:62200932 C>T maps to ENST00000394997 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:73444930 C>T maps to NM_021260.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:78325483 G>A maps to NM_020421.3 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:88974365 T>C did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr14:91806269 G>A maps to NM_001080414.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:42434262 G>A maps to ENST00000397272 V825V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:65759414 G>A maps to NM_197960.2 I577I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:79063929 G>A maps to ENST00000258883 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr15:90774616 G>A maps to NM_006384.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:14738278 C>T maps to NM_016561.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:21272617 C>T maps to NM_001888.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:21721354 C>T maps to ENST00000286149 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:22826362 C>T maps to NM_006043.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:23400345 G>A maps to NM_153603.3 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:28857542 G>A maps to NM_003321.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:58621778 G>A maps to NM_016284.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:67694243 A>G maps to NM_001082486.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:69419339 C>T maps to NM_005652.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr16:69687307 C>T maps to NM_138713.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:2604799 C>T maps to NM_015229.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:5372146 C>T maps to ENST00000457531 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:9580107 C>T maps to NM_153210.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:12860052 C>T maps to NM_014859.4 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:46607196 G>A maps to NM_002144.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:55083550 G>A maps to NM_021626.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:72846042 G>A maps to NM_000835.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:73016474 G>A maps to NM_001545.1 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:74041407 C>T maps to NM_014230.2 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:74093985 G>A maps to NM_001145297.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr17:76115384 G>A maps to NM_007267.6 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr18:13057682 G>A maps to NM_032142.3 W1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr18:32682029 C>T maps to NM_014268.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr18:59888693 T>G maps to NM_020854.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:6427192 C>T maps to NM_173637.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:11533472 G>A maps to NM_145045.4 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:13411422 C>T maps to NM_023035.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:15562864 C>T maps to NM_022904.1 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:36159495 C>T maps to NM_007000.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:42744258 G>A maps to NM_019884.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:46914756 C>T maps to NM_032040.3 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:49132162 C>T maps to NM_020126.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:50046468 G>A maps to NM_020650.2 *329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:50139971 C>A maps to NM_006270.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr19:53668817 G>A maps to NM_024733.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:24521659 T>C maps to NM_006277.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:26533880 G>T maps to NM_001145168.1 Y905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:55882033 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:68592491 A>G maps to NM_002664.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:86459889 G>A maps to NM_022912.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:96943980 C>G maps to NM_014014.3 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:97779538 C>T maps to NM_001164315.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:103142765 C>T maps to NM_001011552.3 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:120438761 G>A maps to NM_030577.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:120725490 T>C maps to NM_002830.2 Y879Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:162273100 G>A maps to NM_006593.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr2:179398126 G>A maps to NM_133378.4 L31837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr20:4768392 C>T maps to NM_014737.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr20:25038495 G>A maps to NM_032501.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr22:38875599 G>A maps to NM_016657.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:33110347 C>T maps to NM_000404.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:39228106 G>A maps to NM_194293.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:77657031 C>T maps to ENST00000332191 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:107474513 C>T maps to NM_001142568.1 Q299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:121251879 G>T maps to ENST00000393672 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:130694261 G>A maps to NM_001001486.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:192516516 G>A maps to NM_178496.3 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr3:196198863 T>A maps to NM_152617.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:1932435 G>A maps to NM_133335.3 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:2900170 C>G maps to NM_014189.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:13543784 C>T maps to NM_001189.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:25253957 C>A maps to NM_018323.3 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:48096181 C>T maps to NM_003328.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:48517100 C>T maps to NM_015030.1 L2627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:49052779 C>T maps to NM_025087.2 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:57173840 C>T maps to NM_020722.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:65194230 A>G maps to NM_001010874.4 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:74453626 G>A maps to NM_201431.1 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:77818387 C>T maps to NM_001029870.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:81207684 G>A maps to NM_004464.3 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:84350761 G>A maps to NM_133636.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr4:165118254 G>A maps to NM_012403.1 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:52096665 C>T maps to NM_015946.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:79025760 G>A maps to NM_153610.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:118274973 C>T maps to NM_173666.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr5:127685048 A>G maps to NM_001999.3 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:27835259 C>T maps to NM_005322.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:31239457 C>T maps to ENST00000383329 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:31695034 G>A maps to NM_013974.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:31842777 G>A maps to NM_025257.2 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:33162524 G>A maps to ENST00000374685 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:36882093 G>A maps to NM_152734.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:41903778 G>A maps to NM_001760.3 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:70944595 C>T maps to NM_001851.4 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:108676918 A>G maps to NM_145315.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:112466046 G>A maps to NM_001105206.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr6:169648583 G>A maps to NM_003247.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:28858776 C>T maps to NM_182898.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:44556400 G>C maps to NM_013389.2 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:92462442 C>T maps to NM_001145306.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:100364684 C>T maps to ENST00000349350 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:107531735 T>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:128630023 G>A maps to ENST00000471166 Q531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:150817138 C>T maps to NM_031946.4 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr7:156746907 C>T maps to NM_138400.1 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr8:53853372 C>T maps to NM_005285.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr8:144997294 C>A maps to NM_201380.2 E2405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr9:98660208 C>T maps to NM_001010895.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr9:130911942 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chr9:140446838 G>A maps to NM_032477.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SN-01A-12D-A22Z-08 chrX:47842406 G>A maps to NM_006962.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:62263048 C>T maps to NM_176877.2 R451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:67890584 G>A maps to NM_001018067.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:89735196 G>A maps to NM_052942.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:100614273 C>T maps to NM_019083.2 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:111216258 C>G maps to NM_002232.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:120056979 C>T maps to ENST00000235547 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:145567754 G>A maps to NM_144698.3 *1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:150972347 G>A maps to NM_001163258.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:176833620 G>C maps to ENST00000281881 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:183853907 C>T maps to NM_015149.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:183920241 G>A maps to NM_015101.2 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:203191374 G>C maps to NM_003465.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:203693082 C>T maps to NM_001001396.1 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:236908073 C>G maps to NM_001103.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr1:247920937 G>A maps to NM_012353.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:7262478 G>A maps to NM_001018039.1 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:73326686 C>T maps to ENST00000398860 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:99770956 G>C maps to NM_018058.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:105780290 C>T maps to NM_014720.2 Q1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr10:119134252 G>A maps to NM_173791.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:1586885 C>G maps to NM_004420.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:17112889 G>A maps to NM_002645.2 F1623F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:21581918 C>T maps to NM_006157.3 C657C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:43380572 C>T maps to NM_018259.5 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:55433226 C>T maps to NM_001004704.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:60154218 C>T maps to NM_206939.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:64670062 G>C maps to ENST00000421419 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:67052908 C>T maps to NM_001619.3 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:68773666 C>T maps to NM_145015.4 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:76066698 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:96074993 G>C maps to NM_032427.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr11:102098266 C>T maps to NM_001130145.2 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:7526236 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:9225251 G>C maps to NM_000014.4 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:10587088 C>T maps to NM_002260.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:12871793 G>T maps to NM_004064.3 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:51389480 G>C maps to NM_001174125.1 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:53292538 C>A maps to NM_002273.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:93100661 G>A maps to NM_001037671.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr12:123789170 G>C maps to NM_001167856.1 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:28127505 C>T maps to NM_153371.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:30782760 C>T maps to NM_032116.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:46594681 G>C maps to ENST00000242848 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:48936982 C>T maps to NM_000321.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr13:92345939 C>G maps to NM_004466.4 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr14:91805716 G>A maps to NM_001080414.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr15:25616709 G>C maps to NM_000462.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr15:30064301 G>A maps to NM_003257.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr15:34064216 G>A maps to NM_001036.3 L2971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr16:22319515 C>G maps to NM_018119.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr16:30506047 C>T maps to NM_002209.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr16:75513366 G>C maps to NM_021615.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:1747275 A>T maps to NM_002945.3 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:1780583 C>T maps to NM_002945.3 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:7369148 C>G maps to NM_020899.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:7579528 C>T maps to NM_001126112.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:10419629 G>A maps to NM_005963.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:26731742 G>C maps to ENST00000440501 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:26732063 G>A maps to ENST00000440501 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:33463471 G>A maps to NM_018096.3 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:39671845 C>T maps to NM_002275.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:40723602 G>A maps to NM_170607.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:40933042 G>A maps to NM_032387.4 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:48696035 C>T maps to NM_018896.3 D1816D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:56233149 C>T maps to NM_012374.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:61514722 G>T maps to NM_001915.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:62864605 G>A maps to NM_199340.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:78314034 C>T maps to NM_020914.4 L2005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr17:80223667 C>T maps to NM_001893.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr18:23915182 G>A maps to ENST00000418698 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:1487785 G>A maps to NM_017573.3 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:1785611 G>A maps to NM_138813.2 I1083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:11489166 C>T maps to NM_000121.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:11890923 G>A maps to NM_152355.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:18174782 G>A maps to NM_005535.1 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:36206115 C>T maps to NM_014383.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:52448419 T>C maps to NM_001031721.3 Y428Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr19:54545035 G>A maps to NM_198481.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:1460026 G>A maps to NM_000547.5 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:74725260 G>A maps to NM_001009812.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:85893859 C>T maps to NM_198843.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:101656804 G>A maps to NM_001102426.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:163076435 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:178528628 C>A maps to NM_016953.3 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:222347093 G>A maps to NM_004438.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr2:233274449 C>G maps to NM_031313.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:35310977 C>T maps to ENST00000373803 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:37524348 C>T maps to NM_015568.2 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:43850440 T>C maps to NM_003008.2 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:50140649 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr20:60878722 G>A maps to NM_175573.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr21:28302317 C>T maps to NM_007038.3 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr21:34804514 C>G maps to ENST00000381995 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr22:17601327 C>T maps to NM_031890.3 W230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr22:30057256 G>T maps to NM_181832.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:42727253 C>T maps to NM_152393.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:44683587 G>A maps to NM_006991.3 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:47385223 G>C maps to NM_025010.4 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:48665890 C>T maps to NM_022911.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:49397642 C>T maps to NM_001664.2 *194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:98538213 G>A maps to ENST00000326857 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:101476574 G>A maps to ENST00000327230 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:113098283 G>A maps to NM_001164496.1 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:118647365 G>A maps to NM_152538.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:121414110 C>T maps to ENST00000393667 E1753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr3:129373851 T>A maps to NM_001017395.3 K536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:1977055 C>T maps to NM_133335.3 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:1991498 C>T maps to NM_005663.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:6711275 G>A maps to NM_203462.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:7016173 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:69870720 A>G maps to ENST00000381096 H481H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr4:186997898 G>A maps to NM_003265.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:10235355 G>T maps to NM_199133.2 Y154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:33596061 G>T maps to NM_030955.2 C877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:35957425 G>C maps to NM_152404.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:36265594 G>C maps to NM_001161429.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:37371052 C>T maps to NM_153485.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:63510307 G>A maps to NM_001113561.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:78944940 C>T maps to NM_173797.3 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:79734014 C>G maps to NM_014733.3 S504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:95011139 C>T maps to NM_031952.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:126214080 C>T maps to NM_178450.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr5:140558544 C>T maps to NM_019120.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:26199399 G>C maps to NM_021065.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:27419546 C>T maps to NM_007149.2 Q597Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:47544788 G>T maps to NM_012120.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:51497405 C>T maps to NM_138694.3 L3874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:57012190 T>C maps to NM_001031623.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:128222208 G>T did not map to a codon.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:151671703 C>T maps to NM_005100.3 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr6:152477103 C>T maps to NM_182961.2 T7973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:23810668 C>T maps to NM_031414.3 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:31018735 G>A maps to NM_000823.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:41739720 C>T maps to NM_002192.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:83823833 C>T maps to NM_006080.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:103018060 C>T maps to ENST00000354356 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr7:151860302 G>A maps to ENST00000355193 F3453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr8:145689920 G>A maps to NM_138496.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:7174704 G>A maps to NM_015061.3 Q1049Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:8485768 C>A maps to NM_002839.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:27561629 G>C maps to NM_018325.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:86917178 G>A maps to NM_022127.2 R154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:94493357 C>T maps to NM_004560.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:95784613 G>A maps to NM_033086.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:109690176 C>G maps to NM_021224.4 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:121929415 C>T maps to NM_014618.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:121930183 C>T maps to NM_014618.2 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:130506923 G>A maps to NM_170600.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:135153599 G>A maps to ENST00000372169 F2233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:137809708 C>G maps to NM_002003.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chr9:139726761 G>A maps to NM_001173988.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chrX:15474082 G>C maps to NM_003662.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chrX:49065841 C>T maps to NM_005183.2 R1622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SO-01A-11D-A22Z-08 chrX:136113173 C>T maps to NM_054021.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:47548039 G>A maps to NM_178134.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:70504188 C>T maps to NM_020794.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:89523876 G>C maps to NM_002053.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:156845926 C>T maps to NM_002529.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:157514226 C>T maps to NM_031281.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:158449926 C>G maps to NM_001004472.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr1:211433477 C>A maps to NM_001136223.1 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr10:1405297 G>A maps to NM_018702.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr10:117228808 C>T maps to NM_207303.2 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:18460093 G>C maps to NM_017448.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:26587102 T>C maps to NM_001135091.1 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:46786764 C>T maps to ENST00000415402 K1151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr11:89133384 G>A maps to NM_016931.3 Q337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:6078421 G>A maps to NM_000552.3 Q2562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:42853913 G>T maps to NM_153026.2 Y731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:49444390 C>A maps to NM_003482.3 E994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:56086672 G>A maps to ENST00000347027 S977S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr12:93100778 C>T maps to NM_001037671.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr14:24546220 G>A maps to NM_006032.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr14:54417547 G>A maps to NM_130850.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr16:10631800 G>A maps to NM_001424.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr17:7576885 C>T maps to NM_001126112.1 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr17:27308686 C>T maps to NM_178860.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr17:40831909 C>A maps to NM_016602.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:8429402 G>C maps to NM_139314.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:9087677 C>T maps to NM_024690.2 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:17367353 G>A maps to NM_031941.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:39805226 G>A maps to NM_020862.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:40902542 C>T maps to NM_181882.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:43763020 G>A maps to NM_002784.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:47236402 G>A maps to NM_001039877.1 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr19:52497323 C>T maps to ENST00000354939 Q346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:73446020 G>A maps to NM_006062.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:219292747 C>T maps to NM_007127.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr2:238296564 G>A maps to NM_004369.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr20:31021671 C>G maps to ENST00000375687 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr22:20073752 G>A maps to NM_022720.6 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr22:32242866 G>A maps to NM_001136029.1 T1014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:48694482 G>A maps to NM_001407.2 S1349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:49136833 G>A maps to NM_005051.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:49394856 G>T maps to NM_000581.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:57658152 G>A maps to NM_152678.2 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr3:186006619 C>T maps to NM_001346.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr4:143044481 C>A maps to NM_003866.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr5:39377091 A>G maps to NM_001343.2 F599F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr5:140222945 G>A maps to NM_018911.2 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr6:28967309 G>A maps to NM_001010877.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr6:129475824 A>G maps to NM_000426.3 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr7:107253834 G>A maps to NM_001008405.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr9:19376293 T>C maps to NM_001010.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr9:106900436 A>G maps to NM_001042550.1 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chr9:139273422 G>A maps to NM_003086.2 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SP-01A-31D-A22Z-08 chrX:77275741 G>C maps to ENST00000355691 G942G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:89845981 G>A maps to NM_198460.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:115118215 G>T maps to NM_005872.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:120254677 C>T maps to NM_006623.3 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr1:155774914 G>A maps to ENST00000368331 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr10:31137575 C>T maps to NM_182755.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr10:135202546 C>T maps to NM_152911.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr11:6290929 C>T maps to NM_176875.2 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr12:266744 C>T maps to NM_001170738.1 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr14:36946211 C>T maps to NM_001101341.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr14:59798178 C>T maps to NM_014992.1 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr17:27447753 G>A maps to NM_078471.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr17:48755295 C>T maps to NM_003786.3 I1190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr19:7117210 A>G maps to NM_000208.2 C1335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr19:8188892 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr19:55816953 G>C maps to NM_032430.1 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr2:121107200 C>T maps to NM_002193.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr2:170011071 G>A maps to NM_004525.2 R4065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr2:234545236 C>T maps to NM_019075.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr21:47531965 G>C maps to NM_001849.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr22:18210179 C>T maps to NM_015367.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr22:46859619 G>T maps to NM_014246.1 C1389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr22:46859880 G>A maps to NM_014246.1 F1302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:46542024 C>G maps to NM_031440.1 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:51266208 A>T maps to NM_004947.4 K589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:127325533 C>G maps to NM_004526.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:140140010 C>T maps to NM_022131.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr3:184062487 C>T maps to NM_144635.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:68514896 G>A maps to NM_018227.5 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:88226450 A>T maps to NM_178135.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:126238268 C>T maps to NM_024582.4 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr4:126239450 C>A maps to NM_024582.4 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:79375840 G>A maps to NM_003248.4 W875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:86679589 C>T maps to NM_002890.1 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:178310334 G>A maps to NM_058230.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr5:178579178 C>T maps to NM_014244.4 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr6:29141693 G>A maps to NM_030905.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chr9:125585293 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SQ-01A-21D-A22Z-08 chrX:70331383 C>T maps to NM_000206.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:7724544 G>A maps to NM_015215.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:40214743 C>G maps to NM_006112.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:208234157 C>A maps to NM_025179.3 E871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr1:248637271 C>T maps to NM_001005495.1 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr10:72300919 C>T maps to NM_014431.2 F657F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr11:64882276 C>G maps to NM_003273.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr11:64884236 C>A maps to NM_014205.2 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr11:117864080 C>T maps to NM_001558.3 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:15807189 G>T maps to NM_004447.5 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:46243817 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:53012245 G>A maps to NM_175068.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr12:56334763 G>A maps to NM_201554.1 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr14:75265974 A>G maps to NM_019589.2 E1325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr16:71220683 C>A maps to NM_032821.2 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr18:50976987 C>T maps to NM_005215.3 I1116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr19:45895560 C>T maps to NM_001142502.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr19:58005152 G>T maps to NM_001098491.1 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr2:105979820 G>A maps to ENST00000344213 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr3:51747291 C>G maps to NM_000839.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr3:52248034 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr4:1985772 C>T maps to NM_005663.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr4:3319745 C>T maps to NM_198229.2 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr4:170608905 C>A maps to NM_173872.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr5:80600668 A>C maps to NM_032280.2 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr5:113698510 G>A maps to NM_021614.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:33284495 C>T maps to NM_001145338.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:37622221 G>T maps to ENST00000297153 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:90573428 T>A maps to NM_012115.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr6:152551704 G>A maps to NM_182961.2 Q7058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr7:30094399 C>G maps to ENST00000440706 S317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr7:47930252 T>C maps to NM_138295.3 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr7:122261660 C>T maps to NM_001167940.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:32633771 G>A maps to NM_153809.2 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:107580988 G>A maps to NM_005502.3 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chr9:137710578 G>A maps to NM_000093.3 P1436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SR-01A-11D-A22Z-08 chrY:4968003 C>T maps to NM_032973.1 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:6181224 G>A maps to NM_015557.2 R1618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:10335484 G>C did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:28477481 G>T maps to NM_001164721.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:42049172 C>T maps to NM_024503.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:43805110 G>A maps to NM_005373.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:47406994 G>A maps to ENST00000371904 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:53755275 C>T maps to NM_004631.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:57489207 G>A maps to ENST00000371231 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:62237175 C>T maps to NM_176877.2 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:101704980 G>A maps to NM_001400.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:109339275 G>A maps to NM_007269.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:110280350 A>T maps to NM_000849.4 L132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:111862082 G>A maps to NM_201653.2 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:145296563 C>G maps to NM_001039703.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:153923846 G>T maps to NM_181715.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:158450383 C>T maps to NM_001004472.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:165648805 G>T maps to NM_000696.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:170959045 T>C maps to NM_001163629.1 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:170965665 G>C maps to NM_001163629.1 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:202097338 C>T maps to NM_004767.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:202703014 C>G did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:207314611 C>T maps to NM_000715.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:220208270 C>T maps to NM_004446.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:241951318 G>A maps to NM_144625.4 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr1:246810439 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:48413871 C>T maps to NM_016204.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:49440293 G>A maps to NM_001018071.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:81932587 T>C maps to NM_145869.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:91469116 C>T maps to ENST00000416354 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr10:102740933 G>C maps to NM_017893.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:18636603 G>C maps to NM_194285.2 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:36302291 G>A maps to NM_014186.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:44098827 G>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:65412520 C>T maps to NM_153253.29 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:66360333 C>T maps to NM_018219.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:66456632 G>A maps to NM_006946.2 Q1990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:68838872 C>T maps to NM_139075.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:88583123 C>T maps to NM_001143831.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr11:130319038 C>T maps to NM_139055.2 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:9229989 G>A maps to NM_000014.4 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:11506648 G>A maps to NM_005039.3 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:20903660 C>T maps to NM_017435.4 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:53242450 G>A maps to NM_173352.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr12:110874485 G>A maps to NM_005719.2 C85C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:20039687 G>A maps to NM_199254.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:46103989 G>A maps to NM_031431.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:114009746 G>T maps to NM_024719.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr13:114077229 G>A maps to NM_138430.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:58604813 G>A maps to ENST00000438670 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:65198191 C>T maps to ENST00000394691 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:88450814 G>A maps to NM_000153.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:102749864 C>G maps to NM_014226.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:105243077 G>T maps to NM_001014432.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr14:105406883 C>T maps to NM_138420.2 K4968K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:34159806 G>A maps to NM_020371.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:41228777 C>T maps to NM_019074.3 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:58256148 G>A maps to NM_003888.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:72581515 G>A maps to NM_052840.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr15:91809816 C>G maps to NM_014848.4 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:783367 C>A maps to NM_022493.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:4797520 G>A maps to NM_139170.2 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:21078641 C>T maps to NM_017539.1 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:66998584 C>T maps to NM_024922.5 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:84199454 G>A maps to NM_178452.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:89800435 C>T maps to NM_001113525.1 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr16:90016034 G>A maps to NM_207514.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:4455915 C>T maps to NM_001105538.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:15532171 C>T maps to NM_006470.3 E484E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:28749807 C>G maps to NM_001304.4 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:34251716 C>T maps to NM_145654.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:34964209 C>T maps to NM_024864.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:38027017 G>T maps to NM_199321.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:40028326 C>T maps to ENST00000401700 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:40039485 C>A did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:43515224 C>T maps to NM_014798.2 *1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:45897372 G>A maps to NM_145798.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:45897591 G>C maps to NM_145798.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:54991172 C>T maps to NM_005082.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:56405155 G>A maps to NM_004758.2 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:62018967 C>T maps to NM_000334.4 E1558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:65052308 C>T maps to NM_000727.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:67519676 C>T maps to NM_002758.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:72297243 C>T maps to NM_023036.4 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr17:72832681 C>T maps to NM_017728.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr18:51898904 C>T maps to ENST00000382911 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:1969890 G>A maps to NM_001319.6 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:14591575 G>A maps to NM_202470.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:22156690 G>C maps to NM_007153.3 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:33334853 G>A maps to NM_014270.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:43382131 G>A maps to NM_006905.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:50864259 C>T maps to NM_004851.1 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:51890571 C>T maps to NM_030657.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:54139968 G>C maps to NM_001012728.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:58370964 C>T maps to NM_032828.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr19:59063423 C>T maps to NM_014453.2 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:1926916 G>A maps to ENST00000399161 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:8870992 G>A maps to NM_020738.2 Q1725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:32264362 G>C maps to ENST00000452582 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:36994258 G>A maps to NM_053276.3 Q170Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:69045055 C>T maps to NM_001007231.2 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:86364194 C>T maps to NM_017952.5 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:112858207 C>T maps to NM_032824.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:122122824 G>A maps to NM_015282.2 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:141533802 C>T maps to NM_018557.2 K1788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:170366330 C>T maps to NM_006063.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:185803227 G>A maps to NM_194250.1 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:197654764 G>A maps to NM_012086.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr2:228881141 C>T maps to NM_001142644.1 V1476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:3838391 G>A maps to NM_020746.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:3869935 G>A maps to NM_153638.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:9459590 G>A maps to NM_001172646.1 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:13514764 G>A maps to NM_017714.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:18297182 C>G maps to ENST00000401790 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:49576559 G>A maps to NM_014484.3 W394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr20:62194087 G>A maps to NM_001037335.2 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr21:42762520 G>A maps to NM_002463.1 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr22:24622207 C>T maps to NM_001099781.1 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr22:40139833 C>T maps to NM_152512.3 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:9776367 C>A maps to NM_001003694.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:9945785 C>T maps to NM_153483.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:11067484 C>T maps to NM_003042.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:43122497 G>A maps to NM_032806.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:45000760 G>C maps to NM_016598.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:45000793 G>A maps to NM_016598.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:46306894 C>G maps to NM_178328.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:58486801 C>T maps to NM_153331.3 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:111603733 C>G maps to NM_001134438.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:115395212 T>C maps to NM_001130064.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr3:194117343 C>T maps to NM_004488.2 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:9783853 G>A maps to NM_000798.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:9783919 C>T maps to NM_000798.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:70359470 G>C maps to NM_021139.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:114276667 G>A maps to NM_001148.4 E2298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:123843691 C>G maps to NM_007083.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:153691891 C>A maps to NM_145720.2 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:153691919 C>T maps to NM_145720.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr4:155665888 C>G maps to NM_004744.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:40852631 C>T maps to NM_032587.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:55178993 C>T maps to NM_139017.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:66386047 A>G maps to NM_001164664.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:112103070 G>T maps to NM_001127510.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:139917810 C>T maps to ENST00000253810 Q2474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:140166144 C>T maps to NM_018900.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr5:180326336 G>C maps to NM_001040462.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:24528377 C>T maps to NM_170740.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:26184091 G>A maps to NM_003523.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:33284066 G>A maps to NM_001145338.1 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:37336787 C>T maps to NM_003958.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:43555014 G>A maps to NM_006502.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:90420472 G>C maps to NM_014611.1 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:105577270 A>G maps to NM_007073.4 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:138619774 G>A maps to NM_020340.4 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr6:158735143 G>A maps to NM_020245.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:99247764 G>C maps to NM_000777.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:116380131 G>A maps to NM_001127500.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr7:149129349 C>T maps to ENST00000440594 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:17813069 C>T maps to NM_006197.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:39537619 C>T maps to NM_014237.2 Q566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:41906304 G>C maps to NM_006766.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:77766228 C>T maps to NM_024721.4 Q2358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:95556076 G>A maps to NM_015496.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr8:100866425 G>A maps to NM_017890.3 A3628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:37948663 C>T maps to NM_003028.2 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:86586834 C>A maps to NM_031262.2 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:102729972 C>T maps to NM_017919.2 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:112042114 G>A maps to NM_019114.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:126143803 C>T maps to NM_020946.1 Q979Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:139873473 C>T maps to ENST00000224167 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chr9:139908490 C>T did not map to a codon.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:15540528 C>T maps to NM_203281.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:55479334 C>T maps to NM_014061.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:102004756 C>T maps to NM_001142530.1 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:105281030 G>A maps to NM_000354.5 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:107319442 A>G maps to NM_001170553.1 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:135593695 G>T maps to NM_014500.4 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:153135919 G>A maps to NM_000425.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FD-A3SS-01A-12D-A22Z-08 chrX:153557915 C>T maps to NM_012253.3 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:23111207 G>A maps to ENST00000400191 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:24857724 C>G maps to NM_013441.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:26073232 G>T maps to NM_020379.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:33058580 C>T maps to NM_001040441.1 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:33272133 T>A maps to NM_003680.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:120930096 G>A maps to NM_001017986.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:150676595 G>A maps to NM_032132.4 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:156047420 C>T maps to NM_001093725.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:171506531 G>A maps to ENST00000392078 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr1:228464925 C>T maps to NM_001098623.1 L2222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:4889678 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:81050723 G>A maps to NM_020338.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:105942271 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:119799754 C>A maps to ENST00000369199 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr10:124339406 C>T maps to ENST00000368915 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:433381 G>A maps to NM_001012302.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:28057954 G>A maps to NM_031217.3 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:44129412 G>T maps to NM_000401.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:47267304 C>T maps to NM_001610.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:59283251 G>T maps to NM_001004711.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:59283287 G>A maps to NM_001004711.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:64010753 C>T maps to NM_057092.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:70201867 G>A maps to NM_003626.2 K813K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:94731430 C>T maps to NM_018039.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr11:125769667 G>A maps to NM_001134793.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:29598223 G>C maps to NM_183378.2 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:52470628 G>A maps to NM_021934.4 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:53216963 G>C maps to NM_175834.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:81746947 C>G maps to NM_003625.2 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:110002953 C>T maps to NM_052845.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:114793705 G>A maps to NM_000192.3 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:117175648 G>A maps to NM_024738.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr12:133420655 C>A maps to NM_001161344.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr13:27216529 G>A maps to NM_006646.5 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr13:76124113 C>T maps to NM_006002.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:23846483 G>A maps to ENST00000339180 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:71374674 C>G maps to NM_014982.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:74523873 C>T maps to NM_025057.2 I497I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr14:95569760 C>T maps to NM_177438.2 K1324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr15:43784618 G>A maps to NM_001141980.1 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr15:72608197 C>T maps to NM_052840.4 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr15:91423193 C>T maps to NM_002569.2 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr16:51173969 C>T maps to ENST00000251020 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:3819556 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:27370278 G>A maps to NM_016518.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:39846393 C>T maps to NM_005801.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:39883362 C>A maps to ENST00000310778 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:45993796 C>T maps to NM_003110.5 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:57262919 G>A maps to NM_018304.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr17:64961110 C>T maps to NM_014405.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:4548447 C>G maps to NM_032108.3 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:34685410 G>A maps to NM_001114093.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:36727427 C>G maps to NM_007145.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr19:56382201 C>T maps to NM_134444.4 F788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:27258519 G>A maps to NM_017727.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:27447626 G>A maps to NM_004341.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:74834256 G>A maps to NM_138804.3 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:95815562 G>A maps to NM_032788.1 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:101584863 C>T maps to NM_002518.3 F343F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:103059777 G>A maps to NM_003853.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:170502385 G>A maps to NM_001085447.1 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:179471895 C>T maps to NM_133378.4 W15243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:203826042 G>A maps to NM_024744.14 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:219209679 G>A maps to NM_015488.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr2:238726128 C>T maps to NM_001080504.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr20:2320504 G>A maps to NM_003245.3 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr20:2819729 T>C did not map to a codon.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr20:57829686 C>T maps to NM_178457.1 A1641A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FJ-A3Z7-01A-12D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr21:33296929 C>T maps to NM_014586.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr21:45837923 C>T maps to ENST00000397932 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr21:46911161 C>T maps to ENST00000359759 V1112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:29092916 G>T maps to NM_001005735.1 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:29940523 G>C maps to NM_003678.4 Y55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:36695010 G>A maps to NM_002473.4 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr22:37868557 G>A maps to NM_002405.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:19479719 C>T maps to NM_144633.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:38601886 C>T maps to NM_001099404.1 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:47956391 C>G maps to ENST00000426837 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:52939152 C>G maps to NM_016329.3 *867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:119562102 T>A maps to NM_002093.3 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr3:151112624 C>T maps to NM_053002.4 L1895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:3237488 C>T maps to NM_002111.6 L2923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:40123291 C>T maps to NM_018177.3 N1187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:71888181 C>T maps to ENST00000504952 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:85742699 G>A maps to NM_014991.4 H376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:106155203 G>A maps to ENST00000513237 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:177058702 C>T maps to NM_170710.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr4:183603123 C>T maps to NM_001080477.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr5:32712403 C>G maps to ENST00000265074 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr5:41840600 C>T maps to NM_000436.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr5:169122826 C>G maps to NM_004946.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:11185603 G>A maps to NM_006403.3 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:29913230 G>C maps to ENST00000376806 *372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:31500658 C>T maps to ENST00000417556 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:88321836 C>G maps to NM_181837.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr6:111628631 G>A maps to NM_002912.3 Q3062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:5353240 G>C maps to NM_001080495.2 L2427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:21599257 G>T maps to NM_003777.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:31611745 C>T maps to NM_194300.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:48349570 C>T maps to NM_152701.3 L3117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:105672956 C>T maps to NM_152750.4 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:107315424 G>A maps to NM_000441.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr7:157926661 G>C maps to NM_002847.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr8:67047318 C>T maps to NM_184085.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr8:77766596 G>A maps to NM_024721.4 T2480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:16437084 G>A maps to NM_017637.5 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:84607085 G>A maps to NM_001001670.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:91090080 G>A maps to NM_006717.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:96015213 G>A maps to ENST00000297954 S628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:103348231 C>T maps to NM_001018116.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:104171808 C>T maps to NM_003452.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:111812855 G>C maps to NM_032012.3 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:127617982 C>T maps to NM_001045476.1 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chr9:130887693 C>T maps to NM_025072.5 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chrX:63411968 C>A maps to NM_152424.3 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chrX:75649247 C>T maps to NM_020932.2 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3Z7-01A-12D-A23M-08 chrX:96854278 C>G maps to NM_006729.4 S1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:1248251 G>A maps to NM_017871.4 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:45480181 C>T maps to NM_000374.4 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:62739458 G>A maps to NM_181712.4 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:91178153 C>A maps to NM_020063.1 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:145561388 C>T maps to NM_144698.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:149785175 G>A maps to NM_001123375.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:155104033 G>A maps to NM_004428.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:157557730 A>G maps to NM_031282.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:158590241 G>A maps to NM_003126.2 F2045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:159802971 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:160209812 C>A maps to NM_015726.3 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:165860505 C>T maps to NM_012474.4 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:178483196 G>A maps to NM_032126.4 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:183933110 C>A maps to NM_015101.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:185278643 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr1:198713181 G>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:17277193 T>C maps to NM_003380.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:64913494 G>T maps to NM_030759.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:75523668 T>A maps to NM_198597.1 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:89472928 C>G maps to NM_001015880.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:98807754 T>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:100185613 C>T maps to NM_000195.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:118228770 T>C maps to NM_001011709.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:126519947 C>T maps to NM_032182.3 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:126683151 G>A maps to NM_022802.2 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr10:135053569 C>T maps to NM_014468.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:9522677 G>T maps to NM_003442.5 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:60635045 C>G maps to NM_207341.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:65417136 G>C maps to NM_153253.29 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:92715237 C>G maps to NM_005959.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:108206597 T>A maps to NM_000051.3 A2726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr11:125221257 C>A maps to NM_022062.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:1940230 G>A maps to NM_001163926.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:55357673 G>T maps to NM_001098815.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:56733305 C>T maps to NM_016584.2 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:57989741 G>C maps to NM_024779.4 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:70070773 G>A maps to NM_032735.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:104327816 C>T maps to NM_003299.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr12:123481052 C>A maps to NM_020845.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr13:99532220 G>T maps to ENST00000428223 Y958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr13:113803476 C>A maps to NM_000504.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:20876346 T>A maps to NM_007110.4 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:21024719 C>T maps to NM_001110361.1 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:37777259 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:57689134 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:76107312 C>A maps to NM_017791.2 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:89148327 C>T maps to ENST00000380664 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:104642733 C>G maps to NM_015656.1 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr14:105354103 G>C maps to ENST00000453495 R1177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:50211047 C>A maps to NM_024837.2 G675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:56152721 G>T maps to ENST00000508342 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:75981329 G>A maps to NM_001897.4 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr15:91500712 G>A maps to NM_033544.2 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:1034809 G>T maps to NM_014587.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:2168841 G>A maps to NM_001009944.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:3140432 C>A maps to NM_032805.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:9014214 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:15133843 T>A maps to NM_173474.2 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:16130385 C>T maps to ENST00000399408 N245N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:20084881 G>T maps to NM_001002911.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:23388688 G>A maps to ENST00000307331 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:27556789 C>G maps to NM_001520.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:58314502 G>A maps to NM_001080492.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:70605035 G>T maps to NM_012426.4 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr16:74452025 T>A maps to NM_001011880.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:34251641 G>A maps to NM_145654.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:56232573 C>G maps to NM_012374.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:63221385 G>A maps to NM_003835.3 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:71426747 C>T maps to NM_001144952.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr17:79207837 C>G maps to NM_144679.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr18:30350104 G>A maps to NM_020805.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:8609324 G>A maps to NM_012335.3 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:9001858 T>C maps to NM_024690.2 R13463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:11609126 C>T maps to NM_138783.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:15121756 G>A maps to NM_173482.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:36303752 C>G maps to NM_021232.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:42132179 T>A maps to NM_001817.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:44636768 A>T maps to NM_013362.2 K668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:45860916 C>G maps to NM_000400.3 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:49863218 G>T maps to NM_003598.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr19:50657921 C>T maps to NM_152358.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:1168817 C>T maps to NM_018968.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:42990185 G>A maps to NM_148962.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:62081095 G>A maps to ENST00000404929 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:96798411 C>A maps to NM_001002036.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:127821518 G>A maps to NM_139343.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:143959729 C>T maps to NM_018460.3 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:179403928 C>T maps to NM_133378.4 K30343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:190428406 C>A maps to NM_014585.5 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:192255218 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr2:216240427 G>A maps to NM_212482.1 G1967G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:2596781 G>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:30672192 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:30672278 G>A maps to NM_002110.3 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:45912356 T>C maps to ENST00000471951 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:50048712 G>A maps to NM_012340.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:62162260 C>T maps to NM_005975.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr20:62337723 C>T maps to NM_003224.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:23626222 G>C maps to NM_004327.3 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:37266563 C>G maps to NM_013416.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:45601540 C>T maps to NM_001009880.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr22:50658875 T>C maps to NM_020461.3 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:19389401 C>A maps to NM_144633.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:38649640 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:150931786 G>A maps to NM_014879.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr3:191074895 C>T maps to NM_178335.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:10084737 C>A maps to NM_017491.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:94343959 T>A maps to NM_001510.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:121958320 G>A maps to NM_024574.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:162463735 C>T maps to NM_020116.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr4:189068456 C>A maps to NM_178556.3 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:10254300 A>C maps to NM_012073.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:131821921 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:140209724 G>A maps to NM_018909.2 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:154393910 G>T maps to NM_001099293.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr5:169101350 G>C maps to NM_004946.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:3154783 C>G maps to NM_001069.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:30571978 C>A maps to NM_002714.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:41621213 G>T maps to NM_005586.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:86227734 T>C maps to NM_153816.3 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr6:129636974 T>C maps to NM_000426.3 S1268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:2404032 G>A maps to ENST00000314800 W342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:101944427 G>C maps to ENST00000306803 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:105190499 A>G did not map to a codon.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:128850353 G>A maps to NM_005631.4 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:149482089 G>A maps to NM_198455.2 Q960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:150878037 C>G maps to ENST00000422024 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr7:158824637 C>T maps to ENST00000402066 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:2944709 A>T maps to NM_033225.5 P2461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:27327364 G>A maps to NM_000742.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr8:54142078 A>G maps to NM_000912.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:21187496 G>A maps to NM_021068.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:33468849 C>A maps to NM_022917.4 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:84607838 G>T maps to NM_001001670.2 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:135553560 G>C maps to NM_012204.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:136323080 G>A maps to NM_139025.3 S1314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chr9:139418226 G>A maps to NM_017617.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chrX:12939699 G>C maps to ENST00000311912 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chrX:57936037 G>A maps to NM_007156.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZE-01A-11D-A23M-08 chrX:77271358 A>G maps to ENST00000355691 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:2529729 C>T maps to NM_033467.3 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:2530148 G>C maps to NM_033467.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:20972085 G>A maps to NM_032409.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:114380325 G>A maps to NM_015967.5 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:154951210 C>T maps to NM_001826.2 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:196250088 G>A maps to NM_198503.2 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:206225297 C>T maps to NM_000707.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr1:248525925 G>A maps to NM_001004696.1 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr10:61830969 C>T maps to NM_020987.2 V3223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr10:124813244 G>A maps to NM_001609.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:17113137 G>A maps to NM_002645.2 R1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:33369460 G>A maps to NM_005734.3 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:75439963 C>G maps to NM_025098.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:89184973 A>G maps to NM_016931.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr11:104897664 C>T maps to NM_033292.2 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:52758101 G>A maps to NM_002283.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:56515126 C>T maps to NM_032786.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:56818909 C>T maps to NM_003920.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:57864226 C>T maps to NM_005269.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:58143280 G>A maps to NM_000075.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:120106159 G>A maps to NM_006253.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr12:130923032 G>A maps to NM_015347.4 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:43816950 C>T maps to ENST00000382031 Q1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:45408926 G>A maps to NM_207581.3 W185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:76958033 T>A maps to ENST00000324767 K869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:90617418 C>T maps to NM_198526.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:91428340 C>T maps to NM_002005.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:99696484 C>T maps to NM_022905.4 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr15:101938608 C>T maps to NM_002570.3 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:18856888 G>A maps to ENST00000389467 I2027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:24803019 G>A maps to NM_014494.2 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:31485479 C>A maps to NM_001042454.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:56436916 C>T maps to NM_001144.4 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr16:87493734 G>A maps to NM_015144.2 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr17:26958633 G>A maps to NM_014680.2 Q1388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr17:31203815 G>A maps to NM_015194.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr17:55027347 G>A maps to NM_004645.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr18:9553377 G>A maps to NM_001042388.1 Q745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr18:33744589 G>A maps to ENST00000442325 W703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:10405104 C>A maps to NM_003259.3 C673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:12154730 G>A maps to NM_001080404.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:16790903 C>T maps to NM_024074.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:17611151 C>A maps to NM_198580.1 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:17611370 C>G maps to NM_198580.1 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:31768031 C>T maps to NM_020856.2 Q889Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:40901225 C>T maps to NM_181882.2 G1011G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:45996514 G>T maps to NM_005619.3 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:48919323 C>T maps to NM_000836.2 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr19:49643308 C>T maps to NM_003660.2 R778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:11338882 C>T maps to NM_004850.3 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:27825412 C>G maps to NM_032434.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:56144827 G>C maps to NM_001039349.1 Y163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:62067208 C>T maps to ENST00000404929 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:101869620 G>A maps to NM_017546.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:157182438 G>A maps to NM_006186.3 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:158406899 T>C maps to NM_145259.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:166850695 C>T maps to NM_001165963.1 W1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:179343040 G>T maps to ENST00000350591 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:179617849 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:220089300 G>C maps to NM_024085.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:220251130 C>T maps to NM_012100.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr2:230377517 G>A maps to NM_139072.3 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr20:48808575 G>T maps to NM_005194.2 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr21:43867193 G>T maps to NM_018961.2 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr22:41553349 G>T maps to NM_001429.3 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:12447408 C>A maps to NM_015869.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:47040468 G>A maps to NM_015175.1 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:49692494 G>T maps to NM_003458.3 E1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:51673631 C>T maps to NM_015106.2 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:58095301 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:112710055 C>T maps to NM_014170.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:119456226 G>A maps to NM_033364.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:158983101 C>T maps to NM_001042705.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr3:196753549 C>T maps to NM_005929.5 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:47574246 G>A maps to NM_020453.3 Q1080Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:62800706 G>A maps to ENST00000506720 K754K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:66356359 C>A maps to NM_004439.5 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:77817829 G>T maps to NM_001029870.1 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr4:146058793 G>A maps to ENST00000447906 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:53815260 C>T maps to NM_052870.2 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:64629867 C>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:72192881 G>C did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:90055401 G>A maps to NM_032119.3 K4039K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:140481672 A>G maps to NM_018937.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:141309810 C>T maps to NM_014773.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr5:161580367 C>A maps to NM_198903.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:26273578 A>T maps to NM_003525.2 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:31675750 G>A maps to ENST00000375834 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:39847177 C>T maps to ENST00000398904 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:42930027 A>G maps to NM_018960.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr6:73951906 G>A maps to ENST00000370385 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr7:100485475 C>T maps to NM_015908.5 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:36693883 G>A did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:77763531 C>T maps to NM_024721.4 L1459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:100443873 G>A maps to NM_017890.3 V1064V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:114327002 A>T maps to NM_198123.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:127569334 G>C maps to NM_174911.4 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr8:145731255 C>T maps to NM_005309.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr9:7798476 C>T did not map to a codon.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr9:101536317 C>T maps to ENST00000375018 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chr9:127113224 G>A maps to NM_001166171.1 *348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chrX:7175543 C>T maps to NM_000351.4 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FJ-A3ZF-01A-11D-A23M-08 chrX:153588565 C>T maps to NM_001110556.1 S1199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:35227229 C>T maps to NM_153212.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:120438647 A>T maps to NM_021794.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr1:247025299 T>A maps to ENST00000428671 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr10:38407013 C>G maps to NM_003421.2 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr10:97141471 G>T maps to NM_001034954.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr11:1463776 C>T maps to NM_003957.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr11:66636411 G>C maps to NM_022172.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr11:105923954 A>G maps to NM_198439.2 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr12:1940431 G>A maps to NM_001163926.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr12:5020961 G>T maps to NM_000217.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr12:131476885 C>T maps to NM_198827.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr13:48985611 G>A maps to NM_005767.5 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr14:104471726 C>T maps to NM_153046.2 I566I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr16:15705591 C>T did not map to a codon.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr16:67262274 G>A maps to NM_014187.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr17:3936217 G>A maps to NM_015113.3 V2221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr17:8417199 C>T maps to ENST00000360416 K839K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr18:28737510 C>G maps to NM_024421.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr19:10099814 T>C maps to NM_015719.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr19:58232718 T>C maps to ENST00000335820 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr2:26624884 C>T maps to NM_145038.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr2:121747296 C>T maps to NM_005270.4 S1269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr20:60714932 G>A maps to NM_002792.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:236601 G>A maps to NM_004168.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:1406323 C>A maps to NM_001044.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:89990018 C>A maps to NM_032119.3 Y2482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:112257851 G>A maps to NM_005669.4 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:171773244 C>T maps to NM_001017995.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr5:179263586 G>A maps to NM_003900.4 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr6:31477643 G>C maps to NM_005931.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr6:37429338 G>A maps to NM_015050.2 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr7:26237280 C>T maps to NM_031243.2 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr7:42005030 G>A maps to NM_000168.5 Q1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr7:100244898 G>A maps to NM_016188.4 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr8:8235549 C>T maps to NM_001080826.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chr9:115652598 G>A maps to NM_033051.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FT-A3EE-01A-11D-A202-08 chrX:128638780 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:2327261 C>T maps to NM_007033.4 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:11854050 G>A maps to ENST00000376585 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:57351742 C>T maps to NM_000562.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:110029716 G>C maps to NM_153340.4 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:120510123 G>C maps to NM_024408.2 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:159825826 G>A maps to NM_001013661.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:211192469 G>A maps to NM_172362.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr1:230903407 C>T maps to NM_006615.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr10:5437319 G>A maps to NM_024803.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr10:72496494 C>T maps to NM_139155.2 F518F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr11:49175903 G>T maps to NM_004476.1 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr11:124482879 T>C maps to NM_052959.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr12:102060549 T>C maps to ENST00000441232 N770N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr12:124345621 C>T maps to NM_207437.3 Y2153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr14:64625482 G>A maps to NM_182914.2 E5311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr14:104177480 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr15:42042439 C>G maps to ENST00000219905 S2261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr15:43896297 C>T maps to NM_153700.2 W1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr16:30997086 C>T maps to NM_025193.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr16:67696466 C>T maps to NM_016948.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:26940460 C>T maps to NM_001174103.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:27008290 C>G maps to NM_003170.3 S456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:37343110 G>A maps to NM_000723.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:45901690 G>C maps to NM_145255.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:54526503 G>A maps to NM_153228.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr17:62864654 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr18:3119939 G>A maps to NM_003803.3 N1015N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr18:43205652 C>G maps to NM_007163.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr19:10395564 C>G maps to NM_000201.2 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr19:39106877 G>A maps to NM_001042600.1 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr19:56953097 C>T maps to ENST00000342634 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr2:20901368 C>T maps to ENST00000381090 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr2:24930107 C>G maps to NM_003743.4 S590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr2:223423424 C>G maps to NM_152386.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:30804434 C>T maps to NM_015352.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:48522406 G>A maps to NM_006038.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:61511414 G>A maps to NM_033081.2 Q1965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr20:61512977 G>A maps to NM_033081.2 L1444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:9146378 G>A maps to NM_014850.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:37033450 G>C maps to NM_014805.3 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:44497014 G>T maps to NM_181489.5 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:51317568 C>T maps to NM_004947.4 L952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:100467339 C>T maps to NM_001007565.2 Q390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:105459360 C>G maps to NM_170662.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:121228969 G>A maps to ENST00000393672 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:155199035 C>T maps to ENST00000340059 K1601K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr3:179294031 G>A maps to NM_004301.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr4:8214431 G>C maps to NM_018986.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr4:83858432 C>G maps to NM_194282.2 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr5:38955779 C>T maps to ENST00000296782 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr5:108290633 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr5:171773244 C>T maps to NM_001017995.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr6:35543682 C>A maps to NM_001145775.1 E435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr6:40360392 G>A maps to NM_020737.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr6:90642372 G>A maps to NM_001170794.1 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr7:42005907 G>A maps to NM_000168.5 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr7:73811472 G>C maps to NM_003388.4 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr8:43197469 C>T maps to NM_001005365.2 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr8:53853372 C>T maps to NM_005285.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr9:125316095 C>A maps to NM_001004457.1 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chr9:133589744 A>G maps to NM_007313.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chrX:47044530 C>A maps to NM_005676.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chrX:53436093 C>A maps to NM_006306.2 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chrX:54022188 G>A maps to NM_001184896.1 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EC-01A-11D-A17V-08 chrX:70470473 G>C maps to ENST00000373988 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:15809800 C>T maps to ENST00000442979 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:15821947 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:21268769 G>A maps to NM_001198801.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:22178282 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:22987516 C>T maps to NM_000491.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:32205545 C>T maps to NM_001703.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:33236756 C>T maps to NM_020888.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:154705585 G>A maps to NM_002249.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:236908061 C>T maps to NM_001103.2 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:238053788 T>C maps to NM_021186.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr1:240071791 G>A maps to NM_000740.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:6258136 G>T maps to NM_004566.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:14939476 G>A maps to NM_001193424.1 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:79740027 C>A maps to NM_007055.3 E1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:124036304 G>A maps to ENST00000368994 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr10:127464240 G>C maps to NM_147191.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:3249789 G>A maps to ENST00000328215 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:3687402 G>A maps to NM_020402.2 F429F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:20181519 G>A maps to ENST00000227256 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:47183187 G>A maps to NM_001003677.1 *338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:55579622 G>A maps to NM_001004738.1 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr11:123848239 A>C maps to NM_001004474.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:344378 G>A maps to NM_016615.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:9346774 C>G maps to NM_002864.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:62790134 G>C maps to ENST00000280377 L877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:75676042 G>A maps to NM_032606.3 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:81111210 C>T maps to NM_005593.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:101017393 C>T maps to NM_174942.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:110024577 T>C maps to NM_001114185.1 H217H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:121867871 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:132426134 G>C maps to NM_025215.5 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr12:132426464 G>C maps to NM_025215.5 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr13:37584736 C>T maps to NM_001014286.2 Q718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr13:103301810 C>G maps to ENST00000376052 S976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr14:22102305 C>T maps to NM_001005466.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr14:62207726 G>A maps to ENST00000394997 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr15:41056392 C>T maps to NM_005258.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr15:41056395 C>T maps to NM_005258.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr15:86790935 C>T maps to NM_152336.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr16:4908645 C>T maps to NM_016936.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr16:67986271 C>A maps to NM_005072.4 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:1703352 G>C maps to NM_052928.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:16327059 C>T maps to NM_016113.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:48068881 C>T maps to NM_005220.2 *288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:49231767 C>T maps to ENST00000393198 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:72436223 C>T maps to NM_022036.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:74388107 G>A maps to NM_022066.3 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr17:77808593 C>A maps to NM_003655.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:4364105 C>T maps to NM_003025.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:7565878 G>T maps to NM_198534.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:9868196 G>C maps to NM_001077624.1 S519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:10561308 C>T maps to NM_001111307.1 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:16337278 C>T maps to NM_001130524.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:24309977 T>C maps to NM_203282.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:38973698 C>T maps to NM_000540.2 V1551V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:42827850 C>T maps to ENST00000406159 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:47219390 C>T maps to ENST00000449438 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:55594760 G>A maps to NM_133180.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr19:55824271 G>A maps to NM_001085488.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr2:48906487 G>A maps to NM_172311.2 K1152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr2:109086466 C>T maps to NM_181453.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:825767 C>T maps to NM_031424.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:23549012 C>T maps to NM_080610.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:36662411 G>A maps to NM_021215.3 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr20:46313303 C>T maps to NM_001161841.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr22:19794229 C>T maps to NM_053004.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr22:23404080 G>A maps to NM_014433.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr22:24472151 C>A maps to NM_012295.3 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:49452276 C>G maps to NM_022171.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:52558713 G>A maps to NM_001134231.1 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:129289673 C>T maps to NM_015103.2 S1235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:138219387 G>A maps to NM_024491.2 Q464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr3:170945998 G>C maps to NM_015028.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr4:25160684 G>C maps to NM_016955.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:41057462 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:66449323 G>A maps to NM_001164664.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:67576547 C>G maps to ENST00000396611 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:133326752 C>T maps to NM_003374.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:134910272 G>A maps to NM_004887.4 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr5:156381552 C>T maps to NM_138379.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:26056392 C>T maps to NM_005319.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:33423780 C>T maps to NM_152735.3 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:56880030 G>A maps to NM_152731.2 W133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:144860467 C>G maps to NM_007124.2 L2136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr6:150048188 C>T maps to NM_198887.1 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:7678738 C>A maps to NM_002947.3 G46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:48318167 T>C maps to NM_152701.3 F2459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:57188659 G>A maps to NM_033273.1 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:73275586 C>G maps to NM_182504.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:81355230 T>C maps to NM_000601.4 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:99312306 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:136935979 G>A maps to NM_002825.5 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr7:140301531 C>T maps to NM_015689.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr8:10466759 G>A maps to NM_178857.5 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr8:121170471 G>A maps to NM_021110.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chr8:143603351 C>T maps to NM_001702.2 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EF-01A-12D-A18F-08 chrX:70514378 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:16255002 C>G maps to NM_015001.2 Y756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:110882242 G>A maps to NM_022768.4 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:145281696 C>T maps to ENST00000454606 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:147124334 G>A maps to NM_016361.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:151131259 C>G maps to NM_024575.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:152882413 G>A maps to NM_005547.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:183853948 C>T maps to NM_015149.3 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr1:203015063 C>G maps to ENST00000367238 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr10:78649234 G>A maps to NM_001161352.1 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr10:102295783 C>T maps to ENST00000442724 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:57075937 G>T maps to NM_033396.2 S1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:59211228 C>T maps to NM_001004728.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:59211278 C>A maps to NM_001004728.1 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:62396346 G>A maps to NM_198335.2 Q714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:83641424 G>C maps to NM_001142699.1 S481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:89028452 G>A maps to NM_000372.4 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr11:132082041 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:53298669 G>A maps to NM_002273.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:109927778 C>G maps to NM_183415.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:109937444 C>G maps to NM_183415.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr12:125834166 C>T maps to NM_052907.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:21175889 C>T maps to NM_175605.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:29599308 T>C maps to NM_001033602.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:53422430 C>T maps to NM_002590.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr13:92560308 C>T maps to NM_004466.4 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:20248954 A>T maps to NM_001005500.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:51378883 C>T maps to NM_002863.4 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:77273019 G>A maps to NM_015305.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr14:95669498 G>A maps to NM_024734.3 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:44788617 G>A maps to NM_016396.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:50152595 G>C maps to NM_024837.2 S1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:65667593 C>A maps to NM_004884.3 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:78566698 C>T maps to NM_018602.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:83447542 C>T maps to NM_001007122.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr15:89402346 G>A maps to NM_013227.3 V2177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:844107 C>T maps to ENST00000455171 D647D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:2546211 C>T maps to ENST00000434757 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:2546964 C>T maps to ENST00000434757 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:24816469 C>T maps to NM_014494.2 Q1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:67298322 C>T maps to NM_004594.2 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr16:67692068 C>T maps to NM_001082486.1 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:3661135 G>C maps to NM_002208.4 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:38173106 C>T maps to NM_000759.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:38253436 G>C maps to NM_021724.3 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:66988370 G>A maps to NM_080283.3 R1221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:73887138 G>C maps to NM_173547.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:76113637 C>T maps to NM_007267.6 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr17:80788478 G>A maps to NM_024702.2 R571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr18:21508632 C>T maps to ENST00000416669 F2782F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr18:77894027 G>A maps to NM_014913.3 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:2097471 C>T maps to NM_001039846.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:8533686 C>T maps to NM_005968.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:10602629 C>T maps to NM_203500.1 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:18705143 C>T maps to NM_004750.4 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:41522599 C>A maps to NM_000767.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:45998200 C>A maps to NM_005619.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:51274255 C>G maps to NM_001506.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:52090204 G>A maps to NM_007147.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:55086013 C>G maps to NM_001130917.1 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr19:55607502 G>A maps to NM_017607.2 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:10712232 C>T maps to NM_024894.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:21228216 A>G maps to NM_000384.2 N3841N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:27162913 C>T maps to NM_020134.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:46583347 G>A maps to NM_001430.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:46583933 G>C maps to NM_001430.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:54080792 G>A maps to NM_006794.2 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:128255776 C>A maps to NM_017969.2 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr2:179622542 G>T maps to NM_133432.3 I3422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr20:2377243 C>T maps to NM_198994.2 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr20:5170442 G>C maps to NM_003818.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr21:34721713 C>G maps to NM_000629.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr21:45726579 C>G maps to NM_002626.4 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr22:19799810 G>A maps to NM_053004.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr22:42209301 C>T maps to NM_024821.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr4:104082503 C>G maps to NM_001813.2 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr4:106157171 T>G maps to ENST00000513237 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr4:187525000 G>C maps to ENST00000260147 S3563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:5182155 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:14746023 G>A maps to NM_054027.4 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:35954390 G>A maps to NM_152404.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:36671302 G>A maps to NM_004172.4 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:80911376 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr5:140755383 G>C maps to NM_018919.2 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr6:151203954 C>T maps to NM_015440.3 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr6:158074649 G>A maps to NM_024630.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr6:160169272 G>C maps to NM_004906.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:20199868 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:31378711 C>T maps to NM_022728.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:38431489 G>A maps to NM_001635.3 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:57193754 T>A maps to NM_033273.1 K78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:76982907 G>T maps to NM_017439.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:82390089 C>G maps to NM_033026.5 V5051V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:86548626 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:89887467 G>A maps to NM_001039706.2 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:94175011 C>T maps to NM_022900.4 N544N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:97821645 C>T maps to NM_014916.3 H623H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:128489028 C>T maps to NM_001458.4 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr7:151846036 C>T maps to ENST00000355193 L4382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:53084871 C>T maps to NM_014682.2 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:68112662 G>A maps to NM_006421.3 L1785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:69030844 C>T maps to NM_024870.2 C1129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:142437046 G>A maps to NM_032611.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr8:144808669 G>A maps to NM_198488.3 F987F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:82335205 G>A maps to ENST00000376537 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:95482947 G>T maps to NM_001003800.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chr9:131504958 G>A maps to NM_006336.2 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:2836236 G>A maps to NM_001669.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:34149300 C>T maps to NM_203408.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:52825555 G>C maps to NM_001009616.2 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:63488785 C>G maps to NM_017677.3 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:70787372 T>C maps to NM_181672.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:120182791 G>T maps to NM_012084.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:125685765 C>A maps to NM_178470.4 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:129148661 G>A maps to ENST00000303743 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EJ-01A-11D-A17V-08 chrX:153880853 C>T maps to NM_020994.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:32797277 C>T maps to NM_004964.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:145103955 C>T maps to NM_004892.4 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr1:186024540 C>T maps to NM_031935.2 T2293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr10:134563025 C>G maps to NM_005539.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr12:53776441 C>G maps to NM_138473.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr14:65259854 C>T maps to ENST00000389723 Q846Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr17:33769075 G>C maps to NM_144682.5 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr17:78166303 C>G maps to NM_024110.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr2:86258590 C>G maps to NM_015425.3 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr2:86258742 C>A maps to NM_015425.3 E1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr20:58545165 C>T maps to NM_177980.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr22:25011026 C>T maps to NM_005265.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr3:14862506 G>A maps to NM_152536.3 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr3:119305345 G>A maps to NM_001125.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr4:13601145 C>A maps to NM_148894.2 E2460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr5:140188973 G>A maps to NM_018907.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr6:26234606 T>C maps to NM_005320.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr6:138198246 G>A maps to NM_006290.2 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr7:84751132 T>C maps to NM_152754.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr7:138310791 G>A maps to NM_001139456.1 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr9:112145728 G>A maps to NM_002829.3 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chr9:140811876 C>G maps to ENST00000277549 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EK-01A-22D-A18F-08 chrX:44870259 C>T maps to NM_021140.2 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:9633410 C>A maps to NM_032315.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:16532691 G>C maps to NM_153213.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:18808554 C>T maps to NM_152375.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:25167379 G>A maps to NM_013943.2 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:36202662 G>C maps to NM_022111.3 S1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:38192826 G>A maps to NM_001099439.1 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:43896195 G>T maps to NM_015284.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:65243753 C>T maps to ENST00000294428 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:110301958 C>T maps to NM_139053.1 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:112309337 G>C maps to NM_007204.4 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:113159452 C>T maps to NM_017744.4 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:115236062 C>A maps to NM_000036.2 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:120461053 C>T maps to NM_024408.2 A1968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:145293518 C>G maps to NM_001039703.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:150960574 C>T maps to NM_003568.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:151261859 C>T maps to NM_020832.1 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:151263515 C>G maps to NM_020832.1 S1182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:155109405 T>C maps to NM_018845.3 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:156912572 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:157514313 C>T maps to NM_031281.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:159284101 G>A maps to NM_001004467.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:160136488 G>T maps to NM_144699.3 E407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:161046191 G>C maps to NM_030916.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:162468056 C>T maps to NM_175866.4 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:166039522 C>T maps to NM_001017961.3 W247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:166845421 C>A maps to NM_053053.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:171251467 G>C maps to NM_002021.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:201981808 C>T maps to NM_004433.4 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:205628643 G>C maps to NM_033102.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:206652435 C>G maps to NM_014002.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:206772965 C>T maps to NM_006893.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:209974758 G>C did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:227149127 C>T maps to NM_020247.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:227923157 G>A maps to NM_053052.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:233314876 G>A maps to NM_014801.3 F1037F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:246811272 G>A maps to NM_152609.2 E590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr1:246923503 C>G maps to NM_016002.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:13154580 C>G maps to NM_021980.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:15121000 C>T maps to NM_001039844.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:43089325 G>A maps to NM_006955.1 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:45877974 C>T maps to NM_000698.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:60145994 G>A maps to NM_003201.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:70719869 G>A maps to NM_004728.2 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:89501081 C>T maps to NM_001015880.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:104678700 C>G maps to NM_017649.3 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr10:116307535 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:618013 G>A maps to NM_021924.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:9435955 C>T maps to NM_006391.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:12341261 C>T maps to NM_032867.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:13435140 C>T maps to NM_032320.5 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:18309161 G>A maps to NM_181507.1 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:26584756 G>C maps to NM_001135091.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:32955537 C>T maps to NM_001076786.1 Q783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:46397142 G>A maps to NM_001105540.1 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:47254408 C>T maps to NM_000107.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:48152047 C>T maps to NM_002843.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:56043551 G>A maps to NM_001004745.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:59271962 C>T maps to NM_001004706.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:62414701 G>C maps to NM_030628.1 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:62415292 G>A maps to NM_030628.1 V753V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:64410026 G>A maps to NM_138734.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:65427189 G>C maps to NM_021975.3 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:67022405 G>A maps to NM_012308.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:73718075 C>T maps to NM_003356.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:75298604 C>T maps to NM_033063.1 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:120169014 C>T maps to NM_014352.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr11:122805333 C>T maps to NM_024806.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:2690860 C>A maps to NM_199460.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:2933048 C>T maps to NM_018463.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:10124257 C>T maps to ENST00000355690 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:12247764 C>G maps to NM_138722.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:20801785 G>A maps to NM_000921.3 L910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:39703447 G>C maps to ENST00000395670 S1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:40629490 G>A maps to NM_198578.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:51323816 G>T maps to NM_014033.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:51467851 C>T maps to NM_030809.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:54367562 G>T maps to NM_014212.3 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:56822357 C>A maps to NM_003920.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:68707439 G>C maps to NM_017440.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:85466778 C>T maps to NM_001079910.1 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:112585912 C>T maps to NM_006700.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr12:124398923 G>A maps to NM_207437.3 L3349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr13:102235650 T>A maps to NM_004791.1 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr13:109613988 C>T maps to NM_015011.1 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:24901327 C>G maps to NM_015299.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:50175882 G>T maps to NM_172193.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:53248519 G>A maps to NM_198066.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:73404760 C>G maps to NM_015604.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:73576062 C>T maps to NM_021239.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr14:74411203 G>C maps to NM_152445.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:22369078 C>T maps to NM_001004719.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:32929005 C>T maps to NM_014783.3 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:42021427 C>T maps to ENST00000219905 R1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:45965960 C>T maps to NM_021199.2 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:58285148 G>A maps to NM_003888.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:71256226 C>T maps to NM_017691.3 Q293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:75014949 C>T maps to NM_000499.3 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr15:90799462 C>T maps to ENST00000438251 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:1741916 G>A maps to ENST00000382711 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:3077241 C>T maps to NM_024339.3 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:3777745 C>T maps to NM_004380.2 T2434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:15718771 G>C maps to NM_014647.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:22157564 G>C maps to NM_173615.3 V913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:24802033 C>T maps to NM_014494.2 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:28603593 G>A maps to NM_001054.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:31075324 G>A maps to NM_001172669.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:31500574 C>G maps to ENST00000431354 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:48237195 G>C maps to NM_032583.3 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:48329967 C>T maps to NM_031490.2 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:53498193 C>G maps to NM_005611.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:57732920 C>T maps to NM_032269.5 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:58319876 C>T maps to NM_001080492.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:58621269 G>C maps to NM_016284.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:66426235 G>C maps to NM_001795.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:67709504 C>T maps to NM_030819.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:67918029 C>T maps to NM_014329.3 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:68293166 C>T maps to NM_012320.3 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:70843805 C>T maps to NM_032821.2 L4920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:74706419 G>C maps to NM_152649.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:74920243 C>A maps to NM_030581.3 E824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:81960751 C>G maps to NM_002661.2 S828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:88706323 C>G maps to NM_013278.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr16:89929888 C>T maps to NM_032451.1 F527F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:2202597 G>A maps to NM_017575.4 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:3779564 G>A maps to ENST00000381771 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:4451466 G>A maps to NM_001105538.1 F565F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:7761958 G>A maps to NM_144607.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:8794165 C>G maps to NM_001142633.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:19642973 G>A maps to NM_000691.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:27228277 G>A maps to NM_144683.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:34073060 G>A maps to NM_139285.2 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:34076185 G>C maps to NM_139285.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:35631156 G>C maps to NM_198834.1 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:38978737 G>A maps to NM_000421.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:39022937 C>T maps to NM_000223.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:39580733 G>A maps to NM_003770.4 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:44144093 G>A maps to NM_015443.3 Q553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:48669296 G>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:54893198 G>A maps to NM_001085430.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:60108954 G>A maps to NM_005121.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:60767310 G>A maps to NM_006039.3 Q1210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:66925207 G>A maps to NM_007168.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:73055612 G>A maps to NM_015353.1 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:74387650 G>A maps to NM_022066.3 F1084F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:76451809 G>A maps to ENST00000389840 F3348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:78115613 G>A maps to NM_014740.3 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr17:78115642 G>A maps to NM_014740.3 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:5398075 G>A maps to NM_012307.2 R806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:12706693 C>G maps to NM_020232.4 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:29848661 C>A maps to ENST00000269209 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:34839144 G>A maps to NM_020180.3 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:43221186 C>A maps to NM_007163.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:44702591 G>T maps to NM_016097.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:47918544 G>A maps to NM_145060.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr18:56585881 G>A maps to NM_018181.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:1068606 G>A maps to NM_012292.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:4453978 C>T maps to NM_025241.2 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:5694464 G>A maps to NM_004793.2 F751F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:6928194 C>T maps to ENST00000381407 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:7569022 C>T maps to NM_198534.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:7968918 C>G maps to ENST00000425613 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:9090785 G>C maps to NM_024690.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:10250948 G>A maps to NM_001130823.1 F1193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:10335095 G>A maps to NM_004230.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:10461568 G>A maps to NM_003331.4 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:11121152 G>A maps to NM_001128849.1 E740E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:12126041 G>T maps to NM_001080411.1 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:13218410 G>A maps to NM_001136035.2 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:17631814 G>A maps to NM_012088.2 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:18684101 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:22940550 A>C maps to ENST00000397104 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:33490609 C>T maps to NM_033103.4 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:34791500 G>A maps to NM_014686.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:36054366 C>T maps to NM_000704.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:36211233 C>T maps to NM_014727.1 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:36230989 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:39804677 G>C maps to NM_020862.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:39882055 G>C maps to NM_017592.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:40902006 G>C maps to NM_181882.2 S751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:41029486 G>C maps to NM_020971.2 L1266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:45262793 C>T maps to NM_005178.4 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:45976194 C>T maps to NM_006732.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:46215529 G>T maps to NM_001080469.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:47535975 C>T maps to NM_002517.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:48801463 G>T maps to NM_144577.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:49436971 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:49661513 G>A maps to NM_017636.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:51293712 C>G maps to NM_033068.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:55420602 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:55570558 G>A maps to NM_001145971.1 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr19:59025543 C>T maps to NM_032792.2 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:29519818 G>A maps to NM_004304.3 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:32678918 C>T maps to NM_016252.3 F1554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:39477776 A>G maps to NM_003618.2 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:39505624 G>A maps to NM_003618.2 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:43992599 C>T maps to NM_172069.3 Q1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:73339500 G>A maps to NM_015470.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:73339599 G>A maps to NM_015470.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:97529514 G>C maps to NM_017789.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:136626326 G>A maps to NM_005915.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:137852589 G>A maps to ENST00000272643 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:153006743 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:165349548 G>C maps to NM_004490.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:175436405 G>C maps to NM_003387.4 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:196718189 C>T maps to NM_018897.2 E2886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:203842023 C>G maps to NM_024744.14 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:216213869 C>T maps to NM_004044.6 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:219532975 G>A maps to NM_022453.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:219920402 C>T maps to NM_002181.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:228174027 C>T maps to NM_000091.4 F1583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr2:228883229 C>T maps to NM_001142644.1 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:854973 G>C maps to NM_015985.2 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:1447414 C>A maps to ENST00000476071 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:18286393 C>T maps to ENST00000401790 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:20177311 C>G maps to ENST00000389655 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:33764070 G>A maps to NM_006404.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:33891805 G>A maps to NM_018244.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:34776318 C>T maps to NM_012156.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:39832341 G>A maps to NM_015035.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:44642134 C>A maps to NM_004994.2 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:45850057 C>A maps to ENST00000471951 G1109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:62198550 G>C maps to NM_001037335.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:62198715 G>C maps to NM_001037335.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr20:62329777 G>A maps to NM_003823.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr21:35183343 G>A maps to NM_003024.2 W795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr21:37833717 G>A maps to NM_001146077.1 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:17624009 C>T maps to NM_033070.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:21138314 G>A maps to NM_000185.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:32188757 C>G maps to NM_001136029.1 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:32627027 C>G maps to NM_014227.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:37902201 G>C maps to NM_014550.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:39483103 G>T maps to NM_021822.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:40661276 C>G maps to ENST00000454349 S362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:46759984 C>T maps to NM_014246.1 K2981K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr22:50523235 C>T maps to NM_015166.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:5246761 G>C maps to NM_014674.2 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:36899291 G>A maps to NM_014831.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:38962666 G>A maps to ENST00000302328 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:48698804 C>G maps to NM_001407.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:49049461 G>A maps to NM_018031.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:52558486 C>T maps to NM_001134231.1 *558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:52696217 C>T maps to ENST00000296302 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:53783405 C>T maps to NM_001128840.1 F1142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:66434682 G>A maps to NM_015541.2 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:100277339 C>T maps to ENST00000403410 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:100961750 G>A maps to NM_016247.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:112185018 G>C maps to NM_181780.3 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:120461333 C>T maps to NM_173825.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:129214428 C>A maps to NM_052985.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:138195289 G>A maps to NM_031913.3 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:139092110 C>T maps to NM_004766.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:151154668 G>A maps to NM_178822.4 I2560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:155633962 C>T maps to NM_003875.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:183225915 G>A maps to NM_130446.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr3:195102745 C>A maps to NM_012287.5 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:37839180 C>T maps to NM_018290.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:56236182 C>T maps to NM_024592.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:62542621 C>T maps to ENST00000506720 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:100503107 C>G maps to ENST00000511045 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:104079968 C>T maps to NM_001813.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:141555213 G>C maps to NM_015130.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr4:186392203 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:7789837 G>A maps to NM_020546.2 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:13862844 G>A maps to NM_001369.2 I1536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:32087405 C>T maps to NM_178140.2 L1284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:37064930 G>A maps to NM_133433.3 L2784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:54922342 C>G maps to NM_173514.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:65349977 C>T maps to ENST00000506030 F944F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:80604426 C>T maps to NM_032280.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:82850805 C>T maps to NM_004385.4 L3228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:133502934 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:140209835 G>A maps to NM_018909.2 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:140580554 T>A maps to NM_018931.2 L403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:140769070 C>G maps to NM_003736.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:145252371 G>A maps to NM_001080516.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:176637916 G>A maps to NM_022455.4 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:176827415 C>T maps to NM_001029886.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr5:180041110 G>A maps to NM_182925.4 D1096D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:7229505 C>T maps to NM_001003699.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:13592070 G>A maps to NM_012241.3 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:26184037 G>A maps to NM_003523.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:29694182 G>T maps to NM_018950.2 *347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:31685394 C>G maps to ENST00000375834 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:31711762 C>G maps to ENST00000375742 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:33380559 G>A maps to NM_024165.2 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:33383646 G>C maps to NM_024165.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:33383742 G>A maps to NM_024165.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:42655959 G>A maps to NM_015255.2 P1620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:43172786 C>T maps to ENST00000354495 F1522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:44219876 C>G maps to NM_007355.2 S535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:46660715 C>G maps to NM_001010870.2 L1617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:46661398 C>G maps to NM_001010870.2 S1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:46996734 G>A maps to ENST00000283297 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:49754285 C>T maps to NM_138733.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:73751753 G>A maps to NM_001160133.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:74150011 G>T maps to NM_138441.2 S345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:90442462 G>A maps to NM_014611.1 F1585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr6:166844057 C>T maps to ENST00000510118 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:2957019 C>G did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:11468660 C>G maps to ENST00000423059 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:44192942 C>T maps to NM_000162.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:44193017 C>A maps to NM_000162.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:48319281 C>T maps to NM_152701.3 L2831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:53104098 C>T maps to NM_182595.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:55873033 G>A maps to NM_207366.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:73588772 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:76984618 G>A maps to NM_017439.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:77256780 C>T maps to NM_002835.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:100087044 C>G maps to ENST00000423930 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:107115257 G>A maps to NM_005295.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:107430025 G>C maps to NM_000111.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:142571844 G>A maps to NM_018646.2 I501I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:150028005 G>A maps to NM_138434.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:150732744 G>A maps to ENST00000297504 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr7:158437064 G>C maps to NM_017760.5 S1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:17739571 G>C maps to NM_201552.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:37728858 G>T maps to NM_001002814.2 S1154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:42179978 G>A maps to NM_001556.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:43197331 C>G maps to NM_001005365.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:48711930 C>T maps to NM_006904.6 Q3378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:67507964 C>T maps to NM_001080416.2 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:98155284 C>T maps to ENST00000325141 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:99234790 C>A maps to NM_024759.1 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:131200402 G>A maps to NM_018482.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:144463987 G>A maps to ENST00000422773 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr8:146156261 G>A maps to NM_006958.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:13224525 G>A maps to ENST00000319217 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:14805088 C>T maps to ENST00000380880 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:37776349 C>T maps to NM_144964.2 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:102722412 C>T maps to NM_017919.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:112144706 C>T maps to NM_002829.3 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:127289099 C>A maps to NM_033334.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:130580996 G>A maps to NM_001114753.1 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:130914209 C>T maps to ENST00000373013 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:131190686 C>T maps to NM_016174.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:131369931 G>T maps to NM_001130438.2 E1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:135776114 G>C maps to NM_000368.4 S871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:138657498 G>A maps to ENST00000298480 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chr9:139937505 C>T maps to ENST00000371600 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2EO-01A-11D-A17V-08 chrX:53106213 C>G maps to NM_018969.5 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:3548888 A>G maps to NM_017818.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:10239489 C>G maps to NM_001105562.2 T1239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:41493985 G>T maps to NM_001031694.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:43636435 C>T maps to NM_001159936.1 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:44461718 C>T maps to NM_152499.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:52874276 G>C maps to NM_032864.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:74670825 T>C maps to NM_003838.3 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:78177466 T>A maps to NM_015017.3 K822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:114196635 A>G maps to NM_001142782.1 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:150679027 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:151020343 G>A maps to NM_017860.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:155145216 G>A maps to NM_173852.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:155247575 C>T maps to NM_020897.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:155490914 C>T maps to ENST00000368346 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:156180071 G>A maps to NM_014655.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:156561601 C>T maps to ENST00000446584 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:161140929 A>C maps to NM_001122764.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:175086246 G>A maps to NM_022093.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:179989992 C>A maps to NM_014810.4 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:196712594 G>A maps to NM_000186.3 V1049V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:205312534 G>C maps to NM_018203.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:206628298 G>A maps to ENST00000414359 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr1:248020676 C>T maps to NM_015431.3 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:17275815 C>T maps to NM_003380.3 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:71129054 C>T maps to ENST00000439900 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:75609036 G>A maps to ENST00000423381 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:101953101 T>G maps to NM_001278.3 S687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:105110682 A>C maps to NM_001011663.1 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr10:118187432 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:556085 C>T maps to NM_173573.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:46895137 T>C maps to ENST00000256991 A1457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:55798059 C>T maps to NM_001001921.1 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:59863128 A>C maps to NM_000139.4 *245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:60636672 C>T maps to NM_207341.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:60889101 G>A maps to NM_014207.3 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:64977855 G>A maps to NM_005186.3 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:71943350 C>T maps to NM_001567.3 H561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:108464257 C>T maps to NM_015065.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:113775662 C>G maps to NM_006028.3 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:120690612 C>T maps to NM_014619.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr11:123676310 G>A maps to NM_001005325.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:15100818 T>C maps to NM_001175.4 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:26810950 G>A maps to NM_002223.2 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:49392961 C>A maps to NM_015086.1 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:53689714 G>A maps to NM_002624.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:57037666 G>A maps to NM_001686.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:65116857 G>T maps to ENST00000418919 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:100378000 C>T maps to NM_152788.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:102569338 A>G maps to NM_017915.3 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:114358487 G>C maps to NM_016196.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:132547110 G>A maps to ENST00000333577 Q2769Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:132547116 G>A maps to ENST00000333577 Q2771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:132547119 G>A maps to ENST00000333577 Q2772Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr12:133381317 G>A maps to NM_005895.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr13:86370508 T>G maps to NM_032229.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr13:108518491 G>A maps to NM_001080396.2 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:20296467 T>A maps to NM_001004723.1 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:20848087 C>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:70512798 C>T maps to NM_183002.1 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:88459415 C>T maps to NM_000153.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:102452340 C>T maps to NM_001376.4 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr14:102493552 T>C maps to NM_001376.4 V2938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:23931698 C>T maps to NM_002487.2 W222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:31239407 C>T maps to NM_017762.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:41280031 T>C maps to NM_017553.1 R1237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:42168428 C>T maps to ENST00000320955 L1335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:43531078 G>A maps to NM_201631.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:73616529 G>T maps to NM_005477.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:76222339 C>T maps to NM_147188.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:78758654 G>A maps to NM_004136.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:86123758 A>T maps to NM_006738.4 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr15:100821442 G>A maps to NM_139057.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:5083317 C>T maps to NM_016256.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:18864944 C>T maps to ENST00000389467 T1576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:19656272 T>C did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:28883958 T>A maps to NM_001145795.1 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:28914208 C>T maps to NM_173201.3 I907I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:29994161 G>A maps to NM_016151.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:31157214 G>A maps to NM_173502.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:31288290 C>G maps to NM_001145808.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:58621688 G>A maps to NM_016284.3 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:69370491 C>G maps to NM_032382.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:70367483 G>A maps to NM_007242.4 *480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:70506487 C>T maps to NM_145059.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr16:89962446 C>T maps to NM_014972.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:7761742 C>T maps to NM_144607.4 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:18513443 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:19316616 A>C maps to NM_007148.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:27076070 C>T maps to NM_004295.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:28506136 A>G maps to NM_032141.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:39925390 C>T maps to NM_021991.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:40025747 T>A maps to ENST00000401700 V1054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:63156667 G>A maps to NM_003835.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:73489995 C>T maps to ENST00000375248 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:73559177 C>T maps to NM_001031803.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:74003726 G>A maps to NM_001988.2 I1853I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:79668079 C>T maps to NM_004712.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr17:79916821 G>A maps to NM_178493.5 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:3255844 A>T maps to NM_006471.2 K149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:13059226 G>C maps to NM_032142.3 S1468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:13069783 C>T maps to NM_032142.3 L1701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:43487975 G>A maps to NM_020964.2 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:72913706 C>T maps to NM_175907.4 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr18:77794533 G>T maps to NM_024805.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:872057 G>T maps to NM_005481.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:4159760 G>A maps to NM_032607.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:17837422 C>T maps to NM_018174.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:18965702 G>A maps to ENST00000418384 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:33072193 G>A maps to NM_004708.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:34919420 C>T maps to NM_005499.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:35758180 C>T maps to NM_205834.2 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:40901698 G>A maps to NM_181882.2 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:42797417 G>A maps to NM_015125.3 K1260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:49652415 G>A maps to NM_003660.2 Q1092Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr19:56388433 G>A maps to NM_134444.4 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:27821011 G>A maps to NM_032434.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:61724136 C>T maps to NM_003400.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:86325856 A>C maps to NM_015425.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:97483117 G>A maps to NM_017623.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:131127378 C>T maps to NM_014369.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:155555299 C>T maps to NM_002239.2 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:179422609 G>T maps to NM_133378.4 L26589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr2:238475308 G>A maps to NM_015893.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:279102 G>T maps to NM_033089.6 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:1286300 C>G maps to ENST00000381876 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:2413167 C>A maps to NM_198994.2 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr20:3052880 G>A maps to NM_000915.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr21:40574386 C>T maps to NM_018963.3 R1483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr21:42780075 G>A maps to NM_002463.1 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr21:47769712 C>T maps to NM_006031.5 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:57107938 C>T maps to NM_181727.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:100103343 C>T maps to NM_014820.3 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:122437770 C>T maps to NM_017554.2 H1591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:142140316 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:148863303 C>T maps to NM_032383.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr3:153847390 G>A maps to NM_015595.3 K384K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:682808 G>A maps to ENST00000404286 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:44709781 C>T maps to NM_138335.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:71459066 C>T maps to NM_016519.4 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:81123530 C>T maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:84364762 C>T maps to NM_133636.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:87770172 G>A maps to NM_197965.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:104066983 A>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:111539517 G>A maps to NM_153426.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:151223936 C>T maps to NM_006726.3 L2630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr4:154243968 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:7867566 T>C maps to NM_024091.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:37059267 G>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:54436169 G>C maps to NM_001170402.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:78280774 G>A maps to NM_000046.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:94245026 T>C maps to NM_024717.4 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:110097169 A>T maps to NM_138773.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:112903524 C>T maps to NM_022828.3 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:132197955 A>G maps to NM_005260.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr5:137622193 G>A maps to NM_001790.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr6:70386121 C>T maps to NM_018368.3 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr6:151857487 G>T maps to ENST00000367290 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:23313137 A>G did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:30197061 G>A maps to NM_152793.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:42964311 C>T maps to NM_002787.4 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:90895379 G>A maps to NM_003505.1 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:138312174 G>A maps to NM_001139456.1 F367F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:143793099 A>G maps to NM_001004135.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr7:151864229 C>T did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:101076155 T>C maps to NM_015668.3 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:145660257 C>T maps to NM_013432.4 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:145697773 C>T maps to NM_145754.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr8:145738371 C>T maps to ENST00000428558 E871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr9:6007546 G>A maps to NM_001017969.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chr9:123852673 G>A maps to NM_007018.4 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chrX:117959284 G>A maps to NM_173798.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A2ES-01A-11D-A17V-08 chrX:133511785 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:110754240 C>T maps to NM_004978.4 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:118537063 G>T maps to NM_206996.2 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr1:158517010 G>T maps to NM_001005189.1 Y295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr11:55322490 T>C maps to NM_001001920.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr11:57996149 G>A maps to NM_001004471.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr11:60229777 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr14:31349662 C>T maps to NM_004086.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr14:88983602 G>A maps to NM_007039.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:48452830 G>T maps to NM_001166131.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr17:79826898 G>A maps to NM_004309.4 Y156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr18:21119388 G>A maps to NM_000271.4 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:10206747 G>A maps to NM_031917.2 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:17972199 C>A maps to NM_000980.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:31040188 G>T maps to NM_014717.1 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:38262255 C>T maps to NM_001172690.1 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr19:46443267 C>T maps to NM_002516.2 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr2:75915022 C>T maps to NM_003203.4 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr2:80101254 G>A maps to ENST00000402739 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr2:122038801 C>A maps to NM_014553.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr3:195975135 G>A maps to NM_005017.2 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr5:79027443 G>T maps to NM_153610.3 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr5:111576459 G>T maps to NM_022140.3 C281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr6:32029937 C>A maps to ENST00000375244 V2388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr6:36652019 C>T maps to ENST00000448526 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr7:148511212 C>A maps to NM_004456.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr8:124787453 C>T maps to NM_144963.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IB-01A-11D-A20D-08 chr9:87366902 C>A maps to NM_006180.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:2938570 G>A maps to NM_080431.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:24768669 C>T maps to NM_020448.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:33987120 G>A maps to ENST00000373381 F3473F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:38003555 G>A maps to NM_024700.2 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:98039505 T>C maps to NM_000110.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:103487274 T>C maps to NM_080629.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:197072566 C>T maps to NM_018136.4 R1938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:204501324 C>G maps to NM_002393.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:210187103 C>G maps to NM_001146261.1 S108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:222833628 C>T maps to NM_198551.2 R1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr1:236205224 C>A maps to NM_002508.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:5798581 C>T maps to NM_017782.4 L2205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:13361207 C>G maps to NM_012247.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:28348589 T>C maps to NM_173496.3 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:50819358 C>T maps to NM_003055.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr10:129899668 C>T maps to NM_002417.4 Q3186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:4608386 C>T maps to NM_001005170.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:10821736 G>C maps to ENST00000429377 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:64514250 G>A maps to NM_005609.2 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:66272177 C>T maps to NM_005700.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:67223205 G>T maps to NM_145200.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:67789326 G>A maps to NM_001161473.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:85630483 C>G maps to NM_173556.3 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:96124928 A>G maps to NM_003772.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:104034598 C>T maps to NM_025208.4 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:108236127 G>T maps to NM_000051.3 E3022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:108236159 G>A maps to NM_000051.3 V3032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:110582891 C>T maps to NM_020809.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:113608338 G>C maps to NM_004724.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr11:117306393 C>T maps to NM_020693.2 K1674K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:2788755 G>A maps to NM_199460.2 E1794E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:21355521 A>G maps to NM_006446.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:50232585 G>A maps to NM_181708.2 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:53045824 C>G maps to NM_000423.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:53621230 G>A maps to NM_000966.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:57637671 C>A maps to NM_145064.1 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:104044295 G>A maps to NM_017564.9 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr12:124401029 C>T maps to NM_207437.3 F3465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr13:77714226 C>T maps to NM_015057.4 Q2491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr13:102359163 C>G maps to NM_004791.1 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:20848599 G>A maps to NM_007110.4 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:23533581 G>A maps to NM_014977.3 I866I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:77242468 G>A maps to NM_014909.4 K255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:88459325 G>A maps to NM_000153.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr14:92471336 G>A maps to NM_004239.3 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:22925787 G>T maps to NM_014608.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:43820097 G>T maps to ENST00000382031 E2381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:48548006 G>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:75308955 G>A maps to ENST00000361900 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:75942837 C>G maps to NM_153271.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:76797228 A>G maps to ENST00000324767 N975N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr15:99459286 G>C maps to NM_000875.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:4310207 C>T maps to NM_003223.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:16297331 G>A maps to NM_001171.5 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:20787319 C>T maps to NM_005622.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:29918390 C>T maps to NM_178863.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:57693504 C>G maps to NM_005682.5 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:57693540 C>G maps to NM_005682.5 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:57693570 C>G maps to NM_005682.5 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr16:74493621 G>C maps to NM_012201.5 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:5009119 C>G maps to NM_014519.2 *445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:8272482 G>C maps to NM_213597.2 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:34856679 G>A maps to NM_001163735.1 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:40317637 G>A maps to NM_012285.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:40321611 G>A maps to NM_012285.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr17:73488565 G>C maps to ENST00000375248 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr18:57363927 C>A maps to NM_133459.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:2042509 C>T maps to NM_199054.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:2933591 C>G maps to NM_021217.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:3620191 C>A maps to NM_021231.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:4910992 C>A maps to ENST00000398240 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:4911004 C>T maps to ENST00000398240 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:6466562 G>A maps to NM_174881.2 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:8615473 C>T maps to NM_012335.3 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:10602629 C>T maps to NM_203500.1 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:16770801 C>T maps to ENST00000358726 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:42583876 C>T maps to ENST00000222339 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:49954845 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:50881972 C>T maps to NM_007121.4 Q223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr19:57335837 C>T maps to NM_006210.2 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:10263126 G>A maps to NM_001165931.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:26706332 C>T maps to NM_194248.2 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:27997347 G>A maps to NM_004891.3 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:45616463 G>A maps to NM_018079.4 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:62066590 G>T maps to ENST00000404929 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:69002383 G>A maps to NM_001007231.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:108994855 C>T maps to NM_006588.2 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:168103797 C>T maps to NM_152381.5 Q1966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:172928566 C>G maps to NM_199227.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:191841751 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:202025317 G>A maps to NM_001127183.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr2:231110621 G>T maps to NM_007237.4 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:30753245 G>C maps to NM_014742.3 *643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:41385231 G>C maps to ENST00000373198 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:44442073 A>G did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:49576334 C>A maps to NM_014484.3 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr20:61041538 C>T maps to NM_080473.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:18933791 C>T maps to NM_001338.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:33069063 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:34640811 C>T maps to ENST00000433395 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:34717649 C>T maps to NM_000629.2 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:41142977 C>G maps to NM_001080444.1 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:43800262 C>A maps to ENST00000380399 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:45743761 C>T maps to NM_002626.4 F537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr21:45948466 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:24376502 G>A maps to NM_000853.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:50530601 G>C maps to NM_018995.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr22:50726222 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:9935059 G>A maps to NM_032492.3 *184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:15297658 G>A maps to NM_004844.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:32582546 T>C maps to NM_016141.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:44763164 C>T maps to NM_033210.4 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:50340339 G>T maps to NM_153281.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:57312521 C>T maps to ENST00000295941 R2808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:87018079 A>G maps to NM_016206.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:113847751 G>A maps to NM_000796.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:124413236 G>A maps to NM_001024660.3 V2488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr3:172165774 G>A maps to NM_198407.2 F143F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G2-A3IE-01A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr4:54968001 G>C maps to NM_133267.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr4:74279156 C>T maps to NM_000477.5 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr5:79965994 C>A maps to NM_002439.3 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:348770 T>C maps to ENST00000457386 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:4943830 C>T maps to ENST00000328908 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:6589065 T>A maps to NM_004271.3 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:10891744 G>C did not map to a codon.
Multiple mappings detected for codon TCGA-G2-A3IE-01A-11D-A20D-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:33408986 G>T maps to NM_006772.2 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:34059675 C>T maps to NM_000841.1 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:34664290 C>T maps to NM_024294.2 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:34985688 C>T maps to NM_015245.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:35211827 G>C maps to ENST00000394681 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:43492226 G>C maps to NM_020750.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:138483237 G>A maps to NM_020340.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr6:160664742 G>A maps to NM_003058.3 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:2978459 C>T maps to NM_032415.4 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:7421177 C>T maps to NM_001037763.2 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:48318543 G>T maps to NM_152701.3 E2585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:86794343 C>A maps to NM_021145.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:105752609 G>C maps to NM_006754.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:105752621 G>C maps to NM_006754.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:139661803 C>T maps to NM_001166253.1 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:148921657 C>G maps to NM_003575.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr7:150068791 C>T maps to NM_001099695.1 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:68044263 G>A maps to ENST00000389042 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:80992660 C>A maps to NM_001025252.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:145736234 C>G maps to NM_138431.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr8:145979131 C>T maps to NM_138367.1 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:117909 G>A maps to NM_207305.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:18928109 G>A maps to NM_153707.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:39178357 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:79324196 G>C maps to NM_015225.2 S998*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:86955490 G>A maps to NM_022127.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:96259827 C>T maps to ENST00000333936 Q294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:131340464 G>T maps to NM_001130438.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chr9:136555521 G>A maps to NM_007101.3 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3IE-01A-11D-A20D-08 chrX:46913970 G>T maps to NM_001077445.1 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:2541194 C>T maps to NM_033467.3 W123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:16262748 G>A maps to NM_015001.2 K3338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:16767291 C>T maps to NM_018090.4 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:22303558 C>T maps to NM_007352.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:26752885 C>G maps to NM_024674.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:32140870 G>A maps to NM_001856.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:33237529 C>G maps to NM_020888.2 S917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:36932896 G>T maps to NM_156039.3 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:38227611 C>T maps to NM_001099439.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:44422328 G>T maps to NM_014652.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:50956337 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:65316593 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:67518489 G>C maps to NM_015139.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:75188927 A>T maps to NM_001889.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:94473257 T>G maps to NM_000350.2 T1979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:110169424 G>C maps to ENST00000393689 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:120539791 C>T maps to NM_024408.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:120539833 A>G maps to NM_024408.2 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:146639437 C>T maps to NM_005399.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:150240427 G>A maps to NM_001077628.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:152281451 A>T maps to NM_002016.1 S1970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:152283395 A>T maps to NM_002016.1 S1322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:156622476 C>T maps to NM_021948.3 R579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:158615286 G>A maps to NM_003126.2 Q1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:160766039 G>A maps to ENST00000263285 Q21Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:162767597 G>A maps to NM_016371.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:167024973 G>C maps to NM_005814.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:171621211 C>T maps to NM_000261.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:173523899 G>C maps to NM_178527.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:204438083 G>A maps to NM_002646.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:212120008 C>T maps to NM_015434.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:214542944 C>T maps to NM_005401.4 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:224804935 C>T maps to NM_152495.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr1:228210568 C>T maps to ENST00000366753 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:15154864 G>C maps to ENST00000378143 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:75011599 G>C maps to NM_016065.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr10:124008641 G>A maps to NM_206862.2 L2877L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:8120356 C>T maps to NM_003320.4 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:9450609 G>A maps to NM_006391.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:18637592 G>C maps to NM_194285.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:62348891 G>C maps to NM_022830.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:64026395 C>G maps to NM_000932.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:64457928 G>A maps to NM_015080.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:64895934 C>T maps to NM_172230.2 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:66458982 G>C maps to NM_006946.2 L1779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:66625619 C>T maps to NM_024036.4 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:89133451 G>A maps to NM_016931.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr11:113286259 G>A maps to ENST00000355319 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:6761553 G>C maps to NM_001127582.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:9305843 C>T maps to NM_002864.2 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:46764967 G>A maps to NM_018976.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:47472632 G>T maps to NM_001143668.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:49226344 G>A maps to NM_004818.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:50195681 C>T maps to NM_001037806.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:52774947 G>A maps to NM_033045.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:56188172 T>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:66698777 C>G maps to NM_033647.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:79837967 A>C maps to NM_005639.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:81647168 C>G maps to NM_024560.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:85517895 G>A maps to NM_001079910.1 K1202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:104049331 C>A maps to NM_017564.9 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:120759996 C>A maps to NM_000928.2 *149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:121018921 G>A maps to NM_015918.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:122825452 G>C maps to ENST00000302528 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:124315200 C>A maps to NM_207437.3 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr12:125284768 G>T maps to NM_005505.4 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:41766847 G>A maps to NM_032138.4 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:46946325 G>A maps to NM_025113.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:58207297 G>A maps to NM_001040429.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:97639536 G>A maps to NM_080818.3 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:99537284 G>A maps to ENST00000428223 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr13:102051407 G>A maps to NM_052867.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:24619593 G>A maps to NM_017999.4 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:61995798 G>C maps to NM_006255.3 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:64467417 C>T maps to NM_182914.2 Q1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:74514681 C>T maps to NM_025057.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:75130692 G>A maps to NM_001039479.1 Q760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:80677656 G>A maps to NM_001007023.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:104552128 G>T maps to NM_001080464.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr14:105954548 G>A maps to NM_001311.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:22993124 C>T maps to NM_014608.2 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:34647760 C>T maps to ENST00000438749 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:38614539 G>T maps to NM_152594.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:43018339 C>A maps to NM_138477.2 E1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:43675566 C>G maps to ENST00000399460 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:56981643 G>C maps to NM_017661.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:65157297 G>A maps to NM_025201.4 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:65917857 C>A maps to NM_004727.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:75108986 C>T maps to NM_021819.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:90784742 C>T maps to NM_001013657.2 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr15:101872077 C>A maps to NM_002570.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:632998 C>T maps to NM_148920.1 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:3100350 C>G maps to NM_022468.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:16349967 C>T maps to ENST00000263012 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:31470892 C>T maps to ENST00000408912 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:48368169 C>T maps to NM_031490.2 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:66651179 C>G maps to NM_178818.2 *235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:66783139 T>A maps to NM_006141.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:76556044 A>G maps to NM_033401.3 E881E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:81077670 C>G maps to NM_015251.2 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:81078382 G>A maps to NM_015251.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:88594546 G>T maps to NM_153813.2 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr16:89799708 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:1564435 G>A maps to NM_006445.3 F1453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:1564633 G>A maps to NM_006445.3 F1423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:4013095 G>C maps to NM_015113.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:4200036 G>A maps to NM_003342.4 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:4498616 C>T maps to NM_001114974.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:8157481 A>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:8808181 G>A maps to NM_001142633.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:18045032 G>C maps to ENST00000205890 L1866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:26824193 C>T maps to NM_001145975.1 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:28380874 G>T maps to NM_198529.3 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:33749639 G>C maps to NM_018042.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:35800674 C>T maps to NM_001166105.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:36523880 C>T maps to NM_014598.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:40336366 G>C maps to NM_001524.1 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:61488929 G>A maps to ENST00000389520 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:67023211 G>C maps to NM_080283.3 S652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:71231890 G>T maps to NM_017941.4 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:72350299 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:73830497 G>A maps to ENST00000412096 Q736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:78111250 G>C maps to NM_014740.3 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr17:79893380 C>T maps to ENST00000432920 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr18:12948140 C>T maps to NM_001013437.1 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr18:63526159 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr18:72345041 C>A maps to NM_017757.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:7615489 G>A maps to NM_001166111.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:8841488 C>T maps to NM_001004699.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:8969427 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:9083459 C>G maps to NM_024690.2 V2785V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:10476363 C>G maps to NM_003331.4 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:10478978 G>A maps to NM_003331.4 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:12155621 G>A maps to NM_001080404.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:12156002 G>C maps to NM_001080404.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:14040948 G>C maps to NM_017721.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:15728815 T>G maps to NM_007253.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:18304801 C>T maps to NM_032683.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:19218756 G>A maps to NM_178526.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:22939879 A>T maps to ENST00000397104 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:33467500 G>C maps to NM_152266.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:36357213 C>A maps to NM_199180.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:39103252 G>C maps to NM_001042600.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:39208628 G>A maps to NM_004924.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:40368510 G>A maps to NM_003890.2 F4279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:40433167 G>A maps to NM_003890.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:42728830 G>A maps to NM_133444.1 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:44571218 C>G maps to NM_013361.4 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:47195049 G>A maps to ENST00000449438 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:48643249 G>C maps to NM_000234.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:49481246 G>C maps to NM_002103.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:51452166 A>G maps to NM_012427.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:52663799 C>T maps to NM_001102657.1 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr19:54937897 C>G maps to ENST00000391739 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:8933972 G>A maps to NM_020738.2 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:26532907 C>G maps to NM_001145168.1 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:28248193 G>A maps to NM_004899.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:36583614 C>T maps to NM_016441.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:46583939 C>G maps to NM_001430.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:54883056 G>T maps to NM_003128.2 E1990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:55559820 C>A maps to ENST00000436346 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:63631243 G>A maps to NM_015910.4 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:71791216 C>T maps to NM_001130987.1 I813I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:73677372 C>G maps to NM_015120.4 S1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:73677409 C>T maps to NM_015120.4 V1251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:74787418 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:80529573 G>T maps to NM_178839.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:86315960 G>T maps to NM_015425.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:86832070 G>C maps to NM_005667.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:109388218 C>T maps to NM_006267.4 L2638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:128016991 T>C maps to NM_000122.1 E699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:133542300 C>A maps to NM_207363.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:160027153 G>T maps to NM_033394.2 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:170050364 C>T maps to NM_004525.2 K2912K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:178705091 C>T maps to NM_016953.3 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:207621667 C>A maps to NM_001039845.1 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:219544718 C>G maps to NM_015690.3 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr2:234072503 C>T maps to ENST00000359570 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:31685466 C>A maps to NM_182519.2 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:32251483 G>T maps to NM_080825.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:35207316 C>A maps to NM_021809.6 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:42355268 G>A maps to NM_176791.3 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr20:62421401 G>A maps to NM_025224.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr21:30307436 G>T maps to NM_015565.2 G1669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr21:35147079 G>T maps to NM_003024.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr22:17468985 G>A maps to NM_001037814.1 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:4856164 G>T maps to ENST00000356617 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:32932039 G>A maps to NM_001039111.1 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:37035094 C>T maps to NM_000249.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:37368569 G>A maps to NM_001172713.1 Q1753Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:38292921 C>G maps to NM_005109.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:39374655 G>A maps to NM_005201.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:42687460 C>T maps to NM_005385.3 Y1461Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:42916915 C>G maps to NM_004391.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:48678957 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:49293673 G>A maps to NM_178173.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:51418782 C>T maps to NM_004947.4 V1962V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:108074153 C>G maps to NM_007072.2 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:123166642 C>T maps to NM_183357.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:190120205 T>C maps to NM_006580.3 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:194371613 G>C maps to NM_018385.2 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr3:195251627 G>A maps to NM_006241.4 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:30724468 C>T maps to NM_001173523.1 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:48078436 G>C maps to NM_003328.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:71824734 C>T maps to ENST00000396051 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:77952016 G>T maps to ENST00000510515 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:83552480 C>G maps to NM_001037582.2 *331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:110384479 C>G maps to NM_006323.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr4:174537199 A>G maps to NM_006792.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:54581606 C>G maps to NM_019030.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:76736793 G>A maps to NM_018268.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:96249153 C>T maps to NM_001130140.1 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:112238166 C>G maps to NM_005669.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:126862373 C>T maps to ENST00000330542 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:140476692 C>T maps to NM_018936.2 I773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:140516662 G>A maps to NM_015669.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr5:147449903 C>T maps to NM_001127698.1 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:31237267 A>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:35443425 G>A maps to ENST00000357281 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:35773513 C>T maps to NM_182548.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:38670779 G>A maps to NM_006708.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:44232768 C>G maps to NM_004556.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:47847058 A>C maps to NM_001013732.3 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:50740450 A>G maps to NM_172238.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:69949066 C>T maps to NM_001704.2 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:70964890 T>G maps to NM_001851.4 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:109766412 C>T maps to NM_022765.3 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:112420506 C>A maps to NM_001033564.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:132910507 G>C maps to NM_003967.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr6:146350755 C>T maps to NM_000838.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:15666537 G>A maps to NM_005924.4 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:87743931 C>G maps to NM_021723.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:100802371 G>A maps to NM_001283.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:100808034 C>T maps to NM_003378.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:123152296 G>C maps to NM_178827.4 S33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:123594166 C>G maps to NM_001174046.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:142459636 G>A maps to ENST00000486171 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:143826870 C>T maps to NM_001001659.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr7:155534733 G>A maps to NM_053043.2 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:3009030 G>T maps to NM_033225.5 T1973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:28196681 C>A maps to NM_006228.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:68536431 C>T maps to NM_020361.4 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:70650367 C>A maps to NM_030958.2 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:75737666 C>T maps to NM_015886.3 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:85441684 A>G maps to NM_001100391.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:87076267 G>A maps to ENST00000276616 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:125487415 C>G maps to NM_007218.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:131140336 C>T did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:133879280 C>T maps to NM_003235.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:134108560 C>T maps to NM_003235.4 L2506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:141525223 G>C did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr8:145140308 G>T maps to NM_003801.3 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:15490122 C>A did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:33797838 G>A maps to NM_007343.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:72892385 C>T maps to NM_015110.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:74489885 C>T maps to NM_016014.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:94487116 G>A maps to NM_004560.2 F553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:103090141 G>T maps to NM_017746.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:139405622 G>C maps to NM_017617.3 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chr9:140166653 C>T maps to NM_015456.3 F489F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:3229460 C>T maps to NM_015419.3 L2261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:11197422 G>A maps to NM_013427.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:48932867 G>A maps to ENST00000322995 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:50377283 G>A maps to NM_020717.3 Q597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:50377641 G>A maps to NM_020717.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:107084380 T>A maps to NM_012216.3 C162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:112033887 C>T maps to NM_001113490.1 Q683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:123518336 T>A maps to NM_001163278.1 G2148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:123680940 C>G did not map to a codon.
Sequencing variant TCGA-G2-A3VY-01A-11D-A22Z-08 chrX:129149534 G>A maps to ENST00000303743 Q929Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:3417235 G>A maps to ENST00000452816 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:6158567 C>T maps to NM_003636.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:84399295 G>A maps to NM_024686.4 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:152188365 G>A maps to NM_001009931.1 H1913H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:157739893 G>A maps to NM_030764.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:160769711 T>A maps to ENST00000263285 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:161789556 G>A maps to NM_007348.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr1:248084483 G>A maps to NM_001005522.1 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr10:16883019 C>T maps to NM_001081.3 A3230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr10:50740775 G>A maps to ENST00000515869 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr10:72360385 C>T maps to NM_005041.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:44296954 G>A maps to NM_021926.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:59415361 C>T maps to NM_152716.2 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:73958133 A>G maps to NM_016147.1 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:92531923 C>T maps to ENST00000298047 P1915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr11:116633512 G>A maps to NM_032725.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr12:13716715 G>A maps to NM_000834.3 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr12:81110944 C>T maps to NM_005593.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr13:25671774 C>G maps to NM_030979.2 S480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr13:29012387 C>T maps to NM_002019.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr13:96743175 C>G maps to NM_153456.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr14:21108980 T>C maps to NM_001001968.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr16:67289056 C>T maps to NM_004594.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr17:10398334 C>T maps to NM_005963.3 T1793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr17:38133154 C>T maps to NM_178171.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr17:46053300 G>A maps to NM_176096.1 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:5212394 G>A maps to NM_002850.3 V1574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:9076789 A>T maps to NM_024690.2 T3552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:22272042 C>T maps to NM_033468.2 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:35551677 C>T maps to NM_182983.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:39971573 G>A maps to NM_001001563.1 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr19:45783635 G>A maps to NM_031417.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr2:11911613 G>A maps to ENST00000396099 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr2:69575327 C>T maps to ENST00000357308 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr20:43142654 T>C maps to NM_006811.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr20:60913288 C>T maps to NM_005560.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr21:47349883 C>G maps to NM_020528.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:49928678 G>A maps to NM_002447.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:49928718 G>A maps to NM_002447.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:49929254 G>A maps to NM_002447.2 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr3:129150349 T>C maps to NM_003925.1 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr4:96761292 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr4:155527887 G>A maps to ENST00000407946 H374H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr5:65118646 G>A maps to NM_020726.4 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr5:79837647 C>T maps to NM_205548.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr6:90421881 G>A maps to NM_014611.1 Y2508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr6:117045537 G>A maps to NM_002269.2 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr7:72848450 G>A maps to NM_003508.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr7:111981065 G>A maps to NM_021994.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr8:139606404 C>T maps to NM_152888.1 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chr9:734745 A>G did not map to a codon.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chrX:90691634 G>A maps to NM_080832.2 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3BM-01A-11D-A22Z-08 chrX:109697192 A>G maps to NM_020769.2 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:34208905 C>T maps to ENST00000373381 K676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:144879255 C>A maps to NM_014644.4 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:144882723 G>A maps to NM_014644.4 Q1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:150679138 G>A maps to NM_032132.4 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:152080268 T>C maps to NM_007113.2 E1808E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr1:247151489 C>T maps to NM_020394.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:71008377 G>A maps to NM_025130.3 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:103534600 G>C maps to NM_033163.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:106960945 G>A maps to NM_014978.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:108371674 C>T maps to NM_001013031.1 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr10:108923756 G>T maps to NM_001013031.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr11:11986169 G>A maps to ENST00000450094 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr11:57135554 C>T maps to NM_002559.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr11:57188793 G>A maps to ENST00000428603 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:14649243 C>T maps to NM_018179.3 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:14923748 C>T maps to NM_175054.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:49435940 G>A maps to NM_003482.3 Q2014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr12:101442179 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr14:71445357 C>T maps to NM_014982.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr14:100166435 G>C maps to NM_006668.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr14:103369713 G>A maps to NM_145725.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr15:25959382 C>T maps to NM_024490.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr16:11076790 G>T maps to ENST00000409790 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr16:20344665 G>T maps to ENST00000424589 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr16:82183008 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:4905367 C>G maps to NM_006612.5 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:27935028 G>A maps to NM_152345.4 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:29557903 C>G maps to NM_001042492.2 S1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr17:31322625 C>T maps to NM_173847.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:3735873 C>G maps to NM_014428.1 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:12542301 C>T maps to NM_005815.4 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:20727611 G>C maps to NM_001159293.1 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:38881043 C>T maps to NM_001042522.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:40928871 G>C maps to NM_013376.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:49622030 G>A maps to NM_018111.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:53958359 C>A maps to NM_001008401.3 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr19:54803052 C>T maps to ENST00000251375 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:11802345 G>A maps to NM_012344.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:39964111 A>T maps to NM_025264.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:71060099 C>T maps to NM_015717.3 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:74842182 G>A maps to NM_138804.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:179497729 G>A maps to NM_133378.4 I11808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:227924257 G>T maps to ENST00000396625 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:230723894 G>C maps to ENST00000389044 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:241710490 G>C maps to ENST00000373308 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr2:242757401 C>T maps to NM_001167599.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr21:18977217 C>A maps to NM_001130914.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr21:45978004 G>C maps to NM_198696.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr22:21384119 C>T maps to NM_004173.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr22:46787590 G>A maps to NM_014246.1 I2029I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr4:6302886 G>A maps to NM_006005.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr4:107268794 G>A maps to NM_001142416.1 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr4:156135696 C>T maps to NM_000910.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr5:79950578 C>T maps to NM_002439.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr5:121767722 G>A maps to ENST00000379533 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr5:176794806 C>T maps to ENST00000398128 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:27775576 C>T maps to NM_003519.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:29274778 C>T maps to NM_030946.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:29640987 G>A maps to NM_001109809.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:90647889 C>T maps to NM_001170794.1 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:111983076 G>A maps to NM_153047.1 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr6:158922866 G>A maps to NM_020245.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:140158899 C>T maps to NM_013446.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:142985598 G>T maps to NM_032982.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:151949044 C>A maps to ENST00000355193 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr7:158827297 G>A maps to ENST00000402066 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:30620853 C>T maps to ENST00000265616 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:36642051 C>T maps to NM_001031836.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:63939793 G>C maps to NM_003878.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:73849755 T>C maps to NM_004770.2 N722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr8:101629925 A>G maps to NM_152628.3 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:84235444 G>A maps to NM_005077.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:130630319 G>A maps to ENST00000223836 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:130742368 G>A maps to NM_001035254.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:139571567 C>A maps to NM_006412.3 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chr9:140151343 G>A maps to NM_015456.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chrX:64959691 G>A maps to NM_002444.2 K557K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chrX:139866321 C>T maps to NM_004065.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chrX:151935356 T>C maps to NM_005362.3 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chrX:151935362 A>G maps to NM_005362.3 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3I6-01A-11D-A20D-08 chrX:153224925 G>A maps to ENST00000369984 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:47840884 C>T maps to NM_016308.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:161132714 G>A maps to NM_012475.4 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr1:186283841 G>A maps to NM_003292.2 Q2319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:5995117 C>T maps to NM_002189.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:50708621 C>G maps to NM_000124.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr10:71871381 C>T maps to NM_018649.2 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:47493802 C>T maps to NM_001172639.1 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:55587677 T>A maps to ENST00000395203 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr11:56380342 G>A maps to NM_001004740.1 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:31604939 G>A maps to NM_144973.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:54901656 C>G maps to NM_005337.4 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr12:111072479 C>T maps to NM_001082538.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr14:21852041 C>T maps to NM_007192.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr14:93125803 C>G maps to NM_024832.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr15:68118510 G>A maps to ENST00000380035 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr15:72552920 C>T maps to NM_020214.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:3977489 C>T maps to NM_015113.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:18167606 G>A maps to NM_148886.1 E309E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:40823446 C>T maps to NM_024927.4 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr17:62248556 G>C maps to NM_018469.3 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:4305977 G>A maps to NM_024333.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:22271789 C>G maps to NM_033468.2 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr19:52497182 G>C maps to ENST00000354939 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr2:170502422 G>C maps to NM_001085447.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr2:231978476 G>A maps to NM_000867.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:22869054 G>A maps to NM_080740.3 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:29966487 G>A maps to NM_003634.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:32506038 C>T maps to NM_000343.3 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr22:44892893 G>C maps to NM_032287.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:14756870 G>A maps to NM_032137.4 W463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:33134910 G>A maps to NM_001039770.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:38591868 A>G maps to NM_001099404.1 S1998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:122259633 G>A maps to NM_031458.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:130293316 G>A maps to NM_001102608.1 K1165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:171404523 G>A maps to NM_002662.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr3:180675619 A>G maps to NM_005087.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr4:175899001 C>T maps to NM_014269.4 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr5:179290666 G>A maps to NM_198868.2 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr6:26188993 C>T maps to NM_003539.3 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr6:32810815 C>T maps to NM_148919.3 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr7:66240336 G>A maps to ENST00000451741 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr7:143018479 G>A maps to NM_000083.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr7:143421795 G>C maps to NM_001130025.1 L837L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr8:125113409 C>T maps to NM_001039112.2 N1652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr9:35062057 C>T maps to NM_007126.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3OO-01A-11D-A22Z-08 chr9:137655582 C>T maps to NM_000093.3 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:45226005 C>T maps to NM_006845.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:52941115 C>T maps to NM_001009881.2 R705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:112525045 C>T maps to ENST00000315987 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:116932064 C>T maps to NM_000701.7 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:150532262 G>A maps to ENST00000369039 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr1:152287124 G>A maps to NM_002016.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr10:1042069 G>C maps to NM_012341.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr11:5878059 G>T maps to NM_001005168.1 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr11:19735318 C>T maps to ENST00000396087 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:2760831 C>T maps to NM_199460.2 S1372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:7459280 C>T maps to NM_001080454.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:49446855 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:104697750 C>T maps to NM_001008394.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:110397700 G>C maps to NM_057169.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:112696954 C>G maps to NM_001109662.2 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr12:122723262 A>G maps to NM_022916.4 N391N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr14:20345190 C>T maps to NM_001005501.1 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr14:75330506 G>A maps to ENST00000445876 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr14:76548710 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr16:2029283 C>G maps to NM_172168.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr16:81914555 G>A maps to NM_002661.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:19451305 G>C maps to ENST00000395585 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:25967774 C>T maps to NM_009587.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:27237352 G>A maps to NM_001033561.1 I750I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:28776729 C>T maps to NM_001304.4 L1011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:44144913 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr17:61787906 G>A maps to NM_001003787.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr18:13826366 G>A maps to NM_005913.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:5600271 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:12779428 C>T maps to NM_016145.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:14150701 C>T maps to NM_004843.2 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:19216401 C>T maps to NM_178526.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:19217161 C>T maps to NM_178526.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:44169568 G>T maps to NM_002659.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr19:49334930 C>T maps to NM_016246.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:85604470 G>A maps to NM_001135023.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:136603936 C>T maps to NM_005915.4 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:167056102 C>T maps to ENST00000303354 E1683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:217124124 G>T maps to NM_020814.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:219736441 G>A maps to NM_006522.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr2:219886643 T>C maps to NM_194302.2 E996E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr20:34063378 C>T maps to NM_007186.3 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr20:62198313 C>T maps to NM_001037335.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr21:43161771 G>A maps to ENST00000352483 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr22:25023475 C>A maps to NM_005265.2 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr3:14508094 G>C maps to NM_001134367.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr3:15045490 C>T maps to NM_003298.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr4:76797580 G>A maps to NM_006239.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr4:114284602 G>A maps to NM_001148.4 E3622E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr4:186380147 T>C maps to NM_152775.3 Q531Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr5:68684859 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr5:175823490 G>A maps to NM_007097.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:1131765 G>A maps to NM_001505.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:30891837 G>C maps to NM_032222.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:90896135 C>T maps to NM_003505.1 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr7:100490232 C>T maps to NM_000665.3 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr8:101719199 G>A maps to NM_002568.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr8:145697779 C>G maps to NM_145754.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr8:145732223 C>T maps to NM_005309.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr9:33943440 G>A maps to NM_018449.2 I564I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GC-A3RB-01A-12D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr9:96214619 C>G maps to ENST00000333936 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chr9:136634578 G>A maps to NM_001134398.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chrX:48650332 G>A maps to NM_002049.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RB-01A-12D-A21Z-08 chrX:101095526 T>C maps to ENST00000263032 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:1235579 G>A maps to NM_030649.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:1267924 G>A maps to NM_152228.1 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:9305293 C>T maps to NM_004285.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:12401927 C>T maps to NM_015378.2 T2906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:16265885 C>T maps to NM_015001.2 I3653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:19439181 G>A maps to ENST00000375267 V3879V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:19992500 G>A maps to NM_000871.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:21940119 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:24408601 G>C maps to ENST00000330966 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:27059193 C>T maps to NM_006015.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:32257897 A>T maps to NM_144569.4 S960S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:33134688 T>C maps to NM_005610.2 H239H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:35227556 C>T maps to NM_153212.2 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:44435912 G>A maps to NM_001384.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:55452005 C>A maps to NM_182532.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:74737352 C>T maps to NM_001112808.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:110199864 G>A maps to NM_000850.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:150307444 G>T maps to NM_004698.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:175334311 G>A maps to NM_003285.2 N807N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:176659285 C>T maps to NM_020318.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:181745298 C>T maps to ENST00000357570 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:185269205 G>A maps to NM_006469.4 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:186057736 G>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr1:246927627 T>C maps to NM_016002.2 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:12197893 A>T maps to NM_018144.3 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:70105548 C>T maps to NM_017987.4 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:81049570 G>A maps to NM_020338.3 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:98307746 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:103990675 C>T maps to NM_005029.3 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:105657329 C>T maps to NM_024928.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr10:123846946 T>C maps to NM_206862.2 P1644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:9167351 G>A maps to NM_015213.2 Y956Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:18048080 A>C maps to ENST00000341556 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:56127856 C>T maps to NM_001005205.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:57947215 G>A maps to NM_001005212.3 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:62301533 C>A maps to NM_001620.1 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:62553844 C>T maps to NM_006473.2 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:73498984 T>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:73681095 C>T maps to NM_153614.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:111749796 C>T maps to ENST00000428306 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr11:118374636 C>G maps to NM_001197104.1 S2677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:569631 C>A maps to NM_173593.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:6637880 G>A maps to NM_014865.3 A1112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:7064629 C>T maps to ENST00000416215 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:29786269 C>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:41337464 T>C maps to NM_001843.2 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:50571653 T>A maps to NM_001113546.1 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:52115496 C>G maps to NM_014191.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:60168666 C>G maps to NM_004731.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:96077359 C>T maps to NM_021229.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr12:123645930 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr13:48985569 T>C maps to NM_005767.5 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:65008895 G>A maps to NM_021979.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:65197645 C>G maps to ENST00000394691 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:94156519 G>A maps to ENST00000393153 L2442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:103465927 G>A maps to NM_006035.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:104165251 G>A maps to NM_005432.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr14:105685545 G>C maps to NM_001519.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:29400576 C>T maps to NM_005503.3 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:40268619 G>A maps to NM_001013703.2 Q608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:41319808 A>G maps to NM_017553.1 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:44067579 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:66587329 G>A maps to NM_001143688.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:73615331 G>A maps to NM_005477.2 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr15:75498409 G>A maps to NM_015492.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:227391 G>A maps to NM_000558.3 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:1817830 C>T maps to NM_015133.3 F1144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:11051689 G>A maps to ENST00000409790 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:27246540 C>T maps to NM_145080.3 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:49672417 G>A maps to NM_015069.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:68009694 G>A maps to NM_022357.3 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr16:90015914 G>A maps to NM_207514.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:5445292 C>T maps to NM_033004.3 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:7490057 C>T maps to NM_004870.3 C117C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:42635139 G>A maps to NM_001466.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:44788429 G>A maps to NM_006178.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:46607196 G>A maps to NM_002144.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr17:76122886 G>A maps to NM_007267.6 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:3982046 G>A maps to NM_001961.3 Y265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:4359176 C>T maps to ENST00000262967 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:7518412 C>G maps to NM_001130955.1 S451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:11038320 G>A maps to NM_024029.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:13220476 C>A maps to NM_001136035.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:13882932 A>G did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:14065246 A>C maps to NM_138353.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:17132939 G>A maps to ENST00000443236 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:18705188 C>G maps to NM_004750.4 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:35993779 G>A maps to NM_033317.4 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:49658509 G>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr19:51883514 C>G maps to NM_030657.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:20405116 G>T maps to NM_001006946.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:98779341 C>T maps to NM_144992.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:120221746 G>A maps to NM_002980.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:128185987 G>A maps to ENST00000409048 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:128324289 C>T maps to ENST00000389524 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:128399646 G>A maps to NM_017980.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:175304648 G>A maps to NM_152529.5 I763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:179587112 A>G maps to NM_133378.4 T6223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:220434967 G>A maps to NM_015311.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:234198933 T>C maps to ENST00000392018 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr2:234545482 A>C maps to NM_019075.2 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:33507278 C>T maps to NM_001076552.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:36937358 C>T maps to NM_001725.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:37353466 C>T maps to NM_080552.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:49510908 G>A maps to NM_181442.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr20:60706475 C>T maps to NM_144703.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:32525012 C>A maps to NM_003253.2 E1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:38139582 C>T maps to NM_000411.5 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:42218551 G>A maps to NM_001389.3 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:43916271 A>G maps to NM_080860.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr21:47953950 G>A maps to ENST00000318711 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr22:37904563 C>T maps to NM_014550.3 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr22:40415994 G>A maps to NM_138435.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr22:42952595 T>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:8607272 A>C maps to NM_014583.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:9785586 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:10400557 G>A maps to NM_001001331.2 R651R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:49053758 C>G maps to NM_001009996.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:54925414 C>T maps to NM_018398.2 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:88040156 A>G maps to NM_000866.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr3:132169585 C>G maps to NM_015268.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:1739042 A>G maps to NM_006342.1 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:6969150 G>A maps to NM_001113361.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:16175862 C>G maps to NM_153365.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:39448238 G>A maps to NM_175737.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:40123216 T>C maps to NM_018177.3 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:87671722 C>T maps to NM_080685.2 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:102946406 G>A maps to NM_017935.4 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:119678895 G>T maps to ENST00000379735 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:146071799 G>C maps to ENST00000447906 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:154216910 C>T maps to NM_015271.3 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:155156344 C>G maps to NM_017639.3 V2698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr4:156850778 T>C maps to NM_001334.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:9119186 C>T maps to NM_003966.2 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:65474671 C>G maps to NM_001077199.1 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:131530658 T>A maps to NM_001142599.1 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:158223454 C>T maps to NM_024007.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr5:176831359 C>T maps to NM_000505.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:25967106 A>G maps to NM_006355.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:33636828 G>T maps to ENST00000374316 T695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:37280748 C>T maps to NM_017772.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:47512340 G>A did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:79577520 C>T maps to NM_001010844.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:90660531 C>T maps to NM_001170794.1 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr6:126236523 C>G maps to NM_181782.4 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr7:16415850 G>A maps to NM_001101426.3 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr7:105752636 G>A maps to NM_006754.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr8:48771463 C>T maps to NM_006904.6 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr8:104897638 C>G maps to NM_001100117.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:6014800 C>T maps to NM_012416.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:6893117 C>T maps to NM_015061.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:34997057 C>A maps to NM_001135005.1 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:91963046 G>A maps to NM_024077.3 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:100862211 C>T did not map to a codon.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:131568172 C>T maps to NM_018201.3 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:131568241 C>G maps to NM_018201.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:131670864 G>A maps to NM_001127244.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:133370344 C>G maps to NM_000050.4 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:136253247 C>T maps to NM_153710.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:136599157 C>T maps to NM_007101.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chr9:137711984 C>A maps to NM_000093.3 L1490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chrX:7811786 G>A maps to NM_013452.2 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chrX:78216655 C>T maps to NM_198333.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chrX:84560910 A>G maps to ENST00000373145 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RC-01A-11D-A22Z-08 chrX:150912795 C>T maps to NM_005140.1 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr1:16053703 G>A maps to ENST00000420314 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr1:37945896 G>T maps to NM_025079.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr1:45242393 G>A maps to NM_001012.1 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr10:73587833 G>A maps to ENST00000373120 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:4869945 G>A maps to NM_001004758.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:5009488 C>T maps to NM_021801.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:67068496 G>A maps to NM_207354.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:105795421 G>T maps to NM_000829.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr11:110035201 G>A maps to NM_033390.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr12:4920040 C>T maps to NM_002235.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr12:117628252 C>T maps to NM_033624.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:48905225 G>T maps to NM_000138.4 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:50158633 G>A maps to NM_024837.2 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:50189506 G>A maps to NM_024837.2 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:52903958 G>A maps to NM_019600.2 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr15:83532987 C>A maps to NM_199330.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr16:54966774 G>A maps to NM_005853.5 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr17:7838453 C>A maps to NM_001037144.4 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:36369486 G>A maps to NM_001024807.1 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:39191750 C>T maps to NM_004924.3 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:45656275 G>C maps to NM_198478.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:51228558 C>T maps to NM_002975.2 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:52498045 G>A maps to ENST00000354939 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr19:56104595 G>A maps to NM_032836.2 F237F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr2:43927131 A>G maps to NM_172069.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr20:34389476 C>T maps to NM_016436.4 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr21:41452088 G>T maps to NM_001389.3 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr21:46875521 G>C maps to ENST00000359759 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr21:47847642 C>T maps to NM_006031.5 L2476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr22:36141975 G>A maps to NM_001082578.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr3:10417248 C>T maps to NM_001001331.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr4:114280166 G>T maps to NM_001148.4 E3465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr5:89923174 G>T maps to NM_032119.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr5:179263551 C>T maps to NM_003900.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr6:62757853 T>A maps to NM_152688.2 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr6:71665844 C>T maps to NM_080742.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr7:6634163 C>T maps to NM_024067.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr7:103007920 G>C maps to NM_002803.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr7:103008416 G>A maps to NM_002803.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr8:104388120 G>A maps to NM_138455.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chr9:118982345 C>A maps to NM_002581.3 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3RD-01A-12D-A22Z-08 chrX:118223491 G>A maps to NM_020721.1 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:50884576 G>A maps to NM_032110.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:99771656 C>T maps to NM_014839.4 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:110581816 C>T maps to NM_033088.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:145438894 G>C maps to NM_006472.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:145439608 G>C maps to NM_006472.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:227921240 G>A maps to NM_023007.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr1:228473944 C>T maps to NM_001098623.1 P3057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr10:28032224 G>A maps to NM_173576.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:1977517 G>A maps to NM_021134.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:55653303 G>T maps to NM_032681.3 E134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:111558771 A>T maps to NM_015191.1 K122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:118382707 C>G maps to NM_001197104.1 S3705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr11:128840031 C>T maps to NM_001142685.1 L1678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:9913401 A>G maps to NM_001781.2 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:39047684 C>T maps to NM_153634.2 *565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:46125014 C>T maps to NM_152641.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:49444141 T>A maps to NM_003482.3 K1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:56349287 G>C maps to NM_006928.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr12:70070716 G>A maps to NM_032735.2 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr14:21486649 G>C maps to NM_201537.1 S276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr14:68228127 C>T maps to NM_015346.3 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr15:40594184 G>C maps to NM_004573.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr15:41388441 G>A maps to NM_017553.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:7577081 C>A maps to NM_001126112.1 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:18394612 G>A maps to NM_001040078.2 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:74774373 C>T maps to NM_024311.2 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr17:79804358 C>T maps to NM_000918.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:13476200 A>G maps to NM_023035.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:17476790 C>T maps to NM_031310.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:36221655 G>A maps to NM_014727.1 W1775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:44378164 C>T maps to ENST00000324394 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:47440646 G>T maps to NM_004491.4 E1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr19:49649226 G>T maps to NM_003660.2 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr2:9637282 G>A maps to NM_003183.4 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr20:16360473 G>A maps to NM_024704.4 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr21:45389126 G>A maps to NM_001037553.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr22:38470961 C>G maps to NM_012407.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr3:64132827 G>A maps to NM_198859.3 F446F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr3:101060533 T>C maps to NM_020654.3 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr4:187540390 G>C maps to ENST00000260147 S2453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:5464639 C>G maps to NM_015325.1 L1731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:68603837 G>A maps to NM_176816.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:68616397 A>C did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:102432326 C>T maps to NM_017676.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr5:128430719 C>T maps to NM_016048.2 F87F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:17675189 G>A maps to ENST00000430136 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:30675514 C>T maps to NM_014641.2 Q947Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:38854692 C>T maps to ENST00000327475 R2784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr6:126210735 C>T maps to NM_181782.4 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:84651767 C>T maps to NM_152754.2 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:111580177 G>A maps to ENST00000428084 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr7:158935194 G>A maps to ENST00000402066 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr8:68956793 G>C maps to NM_024870.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr8:88218311 C>T maps to NM_173538.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr9:336579 A>T did not map to a codon.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chr9:139754395 C>G maps to ENST00000392881 L1167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chrX:111019558 T>C maps to NM_012471.2 Q968Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3WC-01A-31D-A22Z-08 chrX:149013351 T>C maps to NM_005364.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:16579617 G>A maps to NM_018994.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:39799982 C>T maps to ENST00000289893 Q1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:47767247 G>A maps to NM_001048166.1 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:47882466 C>T maps to NM_012186.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:62263086 A>G maps to NM_176877.2 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:67666497 G>A maps to NM_144701.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:110766109 C>T maps to NM_004978.4 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:147095709 C>T maps to NM_004326.2 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:202549681 C>G maps to NM_002481.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:226055672 C>T maps to NM_014698.2 Q143Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:228399582 C>T maps to NM_001098623.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:235969729 G>C maps to NM_000081.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr1:237794756 G>A maps to NM_001035.2 Q2157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr10:46967427 G>A maps to NM_031912.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr10:124402856 C>T maps to ENST00000368915 V2524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr11:36248839 G>A maps to NM_174902.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr11:55541542 G>A maps to NM_001001967.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr11:67051207 C>T maps to NM_001619.3 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:19406894 C>T maps to ENST00000429027 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:27235287 A>G maps to ENST00000398815 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:45173748 G>C maps to NM_001145107.1 S181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:50368530 C>T maps to NM_001652.3 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:50390834 G>C maps to NM_013277.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:56427077 A>T maps to NM_022465.3 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr12:109939196 G>A maps to NM_183415.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr13:37439762 G>C maps to NM_001127217.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr13:95114444 T>A did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr13:113729379 G>A maps to NM_001112732.1 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr14:86089432 A>G maps to NM_013231.4 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr14:93650481 C>A maps to NM_022151.4 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr14:99641435 C>T maps to NM_138576.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr15:75134484 G>A maps to NM_001099436.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr16:27761547 G>A maps to NM_015202.2 V1089V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr16:28840777 G>A maps to NM_148414.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr16:81194495 C>T maps to NM_052892.3 R1164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:556595 C>T maps to NM_001128159.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:3593443 C>T maps to ENST00000435558 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:5009424 G>A maps to NM_014519.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:8141718 C>G maps to NM_025099.5 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:10235463 G>T maps to NM_003802.2 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:10542948 G>C maps to NM_002470.2 L951L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:31324481 C>T maps to NM_173847.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:40939369 C>A maps to NM_032387.4 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:76134202 C>G maps to NM_152468.4 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr17:76167088 C>T maps to NM_004710.3 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr18:21399953 C>G maps to ENST00000416669 S768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:4048229 C>T maps to NM_015898.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:7682675 C>G maps to NM_001080429.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:10488944 G>A maps to NM_003331.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:36128213 G>A maps to NM_024321.3 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:37916854 G>A maps to NM_152484.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:42873013 G>A maps to ENST00000251268 P2167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:47910625 G>T maps to NM_020160.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:55676783 C>T maps to ENST00000301249 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:57327166 A>G maps to NM_006210.2 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr19:58371261 C>T maps to NM_032828.2 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:73993694 G>C maps to NM_003584.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:108626839 T>C maps to NM_021815.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:171356163 C>G maps to NM_138995.3 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:206869541 C>T maps to NM_017759.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:234079248 C>T maps to ENST00000359570 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr2:238277739 G>A maps to NM_004369.3 R1456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr20:390663 C>T maps to NM_031229.2 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr20:36870148 G>C maps to NM_001029864.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr20:60511868 C>T maps to NM_001794.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr21:47809234 C>T maps to NM_006031.5 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr4:82126174 T>C maps to NM_006259.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr4:148406958 C>A maps to NM_001957.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr4:154544212 C>T maps to NM_001131007.1 D1341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:464493 C>T maps to ENST00000315013 N591N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:7520894 G>A maps to NM_020546.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:74970364 C>A maps to NM_001099271.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:80640790 G>A maps to NM_130767.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr5:140348519 C>T maps to NM_018899.5 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:30698321 G>C maps to NM_005803.2 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:30884991 G>A maps to NM_001167734.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:31513917 G>A maps to NM_130463.2 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:31601374 G>A maps to NM_080686.2 R1513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:89388139 T>C did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:102483433 T>C maps to NM_021956.4 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr6:152686042 G>A maps to NM_182961.2 Q3362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr7:72892758 C>T maps to NM_032408.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr7:97944888 G>T maps to NM_018842.4 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr7:116869838 C>G maps to ENST00000323984 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:11405587 C>A maps to ENST00000427279 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:36644852 G>A maps to NM_001031836.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:38677878 C>T maps to ENST00000379931 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:48740728 C>T maps to NM_006904.6 Q2858Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:59506849 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr8:69358638 C>G maps to NM_052958.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:35094273 G>T maps to NM_032634.2 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:35094309 G>A maps to NM_032634.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:35735134 G>C maps to NM_006368.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chr9:140250820 C>G did not map to a codon.
Sequencing variant TCGA-GC-A3YS-01A-11D-A23M-08 chrX:154736680 G>A maps to NM_018196.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:1221397 C>T maps to NM_001130413.2 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:10715771 G>A maps to NM_001079843.1 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:11740481 G>A maps to ENST00000376669 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:27097693 C>T maps to NM_006015.4 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:35917361 C>T maps to NM_024874.4 V643V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086420 C>G maps to NM_031936.4 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086531 C>T maps to NM_031936.4 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086714 C>G maps to NM_031936.4 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110086723 C>T maps to NM_031936.4 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:110255279 C>G maps to ENST00000369812 S26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:145561859 G>A maps to NM_144698.3 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:150482399 C>T maps to ENST00000369049 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:154544294 G>A maps to NM_000748.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:158589082 G>C maps to NM_003126.2 V2153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:158725150 C>T maps to NM_001005184.1 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:172628517 G>A maps to NM_000639.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:204401356 C>A maps to NM_002646.3 E1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:204956660 T>C maps to ENST00000367172 Y969Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr1:223175803 A>G maps to NM_032890.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:11207532 G>A maps to NM_006561.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:50947853 G>T maps to NM_018245.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:69281695 G>C maps to NM_013266.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:71144658 G>A maps to ENST00000439900 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:75301467 G>A maps to NM_152586.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:76993968 C>T maps to NM_144589.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:96018854 C>G maps to ENST00000371380 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr10:98064409 C>T maps to NM_004088.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:33631369 G>T maps to ENST00000389726 G1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:45671792 G>C maps to NM_003654.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:57379281 C>T maps to ENST00000403558 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:63971070 G>A maps to ENST00000358794 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:66083094 C>T maps to NM_020404.2 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:70194496 G>T maps to NM_003626.2 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr11:77629998 G>C maps to NM_033547.3 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:15262115 C>T maps to NM_032918.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:49434817 G>C maps to NM_003482.3 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:55794818 C>A maps to NM_001005518.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:56998907 G>A maps to NM_013449.3 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:103246653 G>A maps to NM_000277.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr12:124236903 A>T maps to NM_012463.3 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:75469785 C>T maps to NM_014239.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:77861082 G>C maps to NM_001113475.1 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:95562204 G>A maps to NM_177438.2 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr14:100793637 C>T maps to NM_207117.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr15:56950641 C>T maps to NM_017661.2 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr15:67649728 G>C maps to NM_001031715.2 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr16:1828496 G>A maps to NM_080861.3 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr16:50118103 G>T maps to NM_182922.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr16:54966651 C>T maps to NM_005853.5 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:7680152 G>A maps to NM_020877.2 L1668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:26966616 G>C maps to NM_014680.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:27235834 C>T maps to NM_001033561.1 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:27379940 G>A maps to NM_016518.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:35479508 G>A maps to NM_198834.1 R2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr17:79891090 C>G maps to ENST00000432920 *347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr18:29867521 C>T maps to ENST00000269209 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr18:33689639 C>T maps to NM_012319.3 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr18:51851179 G>C maps to NM_139171.1 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:1978448 C>T maps to NM_001319.6 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:12954348 C>T maps to NM_014975.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:17373411 C>T maps to NM_031941.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:33202725 G>T maps to NM_001105570.1 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:38966026 C>G maps to NM_000540.2 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:41206058 C>T maps to NM_024876.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:41354575 C>A maps to NM_000762.5 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:44936419 G>C maps to NM_014518.2 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:49425625 C>G maps to NM_006184.5 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr19:53303585 G>A maps to NM_006969.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:21225672 T>C maps to NM_000384.2 K4207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:37487527 C>G did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:54856190 C>T maps to NM_003128.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:128399743 C>A maps to NM_017980.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:140990859 T>C maps to NM_018557.2 L4565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:166003407 C>T maps to NM_006922.3 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:166019258 C>G maps to NM_006922.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:166627185 T>A maps to NM_004482.3 K9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:167151172 C>T did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:174231088 C>T maps to NM_031942.4 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:179451490 G>A maps to NM_133378.4 T18811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:206480356 G>A maps to ENST00000406610 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:220367144 G>A maps to ENST00000373917 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:236617865 C>T maps to NM_001037131.1 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr2:242128094 G>A maps to NM_001001891.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr20:52645062 G>A maps to NM_003657.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr21:16337171 C>T maps to NM_003489.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr21:45161559 G>A maps to NM_003681.4 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr22:19951776 C>G maps to NM_001135162.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr22:26761375 G>T maps to NM_021115.4 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:99567198 G>A maps to NM_001042459.1 V1107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:124646787 C>G maps to NM_033049.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:180349346 C>T maps to NM_181426.1 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr3:195594700 G>C maps to NM_001010938.1 S886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:33683978 G>A maps to NM_030955.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:98115320 A>G maps to NM_001012761.2 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:131925438 G>A maps to NM_005732.3 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:131925447 G>A maps to NM_005732.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr5:138386693 G>A maps to ENST00000509534 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:4131045 G>A maps to NM_206836.2 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:7583320 C>A maps to NM_004415.2 L1942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:25972224 G>A maps to NM_006355.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:26123850 C>T maps to NM_003526.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:29576386 G>A maps to NM_001470.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:33283568 G>A maps to NM_001145338.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:44254252 C>T maps to NM_182539.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:136667000 C>T maps to NM_001198609.1 Q774Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr6:153316426 C>A maps to NM_019041.5 E123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:4917470 G>T maps to NM_018059.4 Y100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:21920408 G>A maps to NM_003777.3 L4102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:22533266 C>T maps to ENST00000441815 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:135262737 C>T maps to NM_015135.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr7:143701977 G>T maps to NM_001005281.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr8:71508502 C>G maps to NM_014294.5 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr8:73848918 C>T maps to NM_004770.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr9:117093119 G>A maps to NM_000608.2 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr9:135778174 C>G did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chr9:140196036 C>T maps to NM_001004354.2 *115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chrX:44966653 G>A did not map to a codon.
Sequencing variant TCGA-GD-A2C5-01A-12D-A17V-08 chrX:106359926 C>T maps to NM_018301.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:28863400 G>A maps to NM_001048194.2 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:44450628 C>T maps to ENST00000309519 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:46027484 C>T maps to NM_153326.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:70503870 T>C maps to NM_020794.2 N750N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:92515896 C>T maps to NM_173567.4 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:114128165 T>G maps to NM_001142782.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:150131672 C>G maps to ENST00000443480 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:151015531 G>A maps to NM_138278.3 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:154234111 G>A maps to NM_014847.3 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:154698405 G>A maps to NM_002249.4 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:158687407 C>A maps to ENST00000368146 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:169351298 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:186094826 A>G maps to NM_031935.2 T4197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:197641246 T>G maps to NM_001195215.1 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:201061109 C>T maps to NM_000069.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:223959544 C>T maps to NM_001748.4 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:226034878 C>T maps to NM_014698.2 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:236180523 G>A maps to NM_002508.2 I726I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:238049173 G>A maps to NM_021186.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:248436918 G>A maps to NM_001004695.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr1:248685807 C>T maps to NM_001013355.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:5808245 G>A maps to NM_001494.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:22830754 G>C maps to NM_005028.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:26800719 G>A maps to NM_019043.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:27423783 G>A maps to NM_139312.1 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:35317751 T>A maps to NM_001198778.1 K554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr10:131671830 G>A maps to ENST00000355311 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:20113768 G>T maps to ENST00000396087 L1949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:56020431 T>C maps to NM_001004747.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:57799185 C>T maps to NM_001005186.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:65318915 C>T maps to NM_001130144.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:66313209 G>A maps to NM_207340.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr11:121414361 C>T maps to NM_003105.5 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:1895204 C>T maps to NM_024551.2 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:49054187 C>T maps to NM_017822.3 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:50829319 C>T maps to ENST00000429001 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:51500366 G>A maps to NM_005653.4 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:52984644 G>C maps to NM_080747.2 S355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:53994748 C>A maps to NM_001130059.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:57398641 G>C maps to NM_014830.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr12:71960692 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:25008865 C>T maps to NM_006437.3 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:46708312 C>T maps to NM_002298.4 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:72053439 C>T maps to ENST00000359684 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:96274733 G>A maps to NM_198968.2 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:97999161 A>G maps to ENST00000376673 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr13:100637332 G>A maps to NM_007129.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr14:21960462 G>A maps to NM_014828.2 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr14:56122762 G>A maps to NM_001079521.1 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr14:99183485 G>T maps to NM_182560.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:28408391 G>A maps to NM_004667.4 Q3532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:51772765 G>C maps to NM_001174116.1 L2179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr15:89403659 C>T maps to NM_013227.3 H2312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:1417785 C>G maps to ENST00000508903 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr16:30134419 G>A maps to NM_002746.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:7674652 C>T maps to NM_020877.2 I1456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:8659710 C>T maps to NM_001128076.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:29220309 A>T did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:42397440 G>A maps to NM_001143780.1 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:60059761 G>T maps to NM_005121.2 S1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr17:60059865 G>T maps to NM_005121.2 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr18:19239255 C>T maps to NM_138340.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr18:40850419 G>A maps to NM_020783.3 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:8056715 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:14028881 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:14910474 G>C maps to NM_198944.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:14992002 G>C maps to NM_030901.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:15508412 C>T maps to NM_014371.2 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:42490309 C>T maps to ENST00000441343 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:44891131 C>T maps to NM_152354.3 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:49643259 G>A maps to NM_003660.2 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:50666220 C>A maps to NM_152358.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:53644298 C>T maps to NM_001172674.1 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr19:59022229 G>A maps to NM_012254.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:27900719 G>A maps to NM_018158.2 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:85836115 G>C maps to NM_001013649.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:95537569 C>T maps to NM_144705.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:99413947 C>T maps to NM_207362.2 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:152553183 T>C maps to NM_001164507.1 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:179482572 G>A maps to NM_133378.4 A13267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:179577066 G>T maps to NM_133378.4 S7950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:190333284 G>A maps to NM_032168.1 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:216965209 C>G maps to NM_138390.3 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr2:220077976 G>A maps to NM_005689.2 F597F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:3128234 G>C maps to NM_021826.4 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:3562948 G>A maps to NM_139321.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:33356290 C>A maps to NM_014071.2 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr20:42162961 G>A maps to NM_032107.4 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr22:25599846 C>G maps to NM_004076.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr22:31533773 G>A maps to NM_015715.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr22:36712696 C>T maps to NM_002473.4 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:11301167 C>T maps to NM_001098211.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:42226216 C>A maps to NM_001042646.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:42226283 C>T maps to NM_001042646.1 I157I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GD-A3OP-01A-21D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:57908653 G>A maps to ENST00000428312 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:74535679 T>C maps to NM_020872.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:98002336 A>G maps to NM_001005482.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:98217063 T>C maps to NM_001004737.1 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:112299548 C>T maps to NM_017945.2 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:132418249 C>T maps to ENST00000393156 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:156395593 G>A maps to NM_015508.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:179080189 G>A maps to NM_033540.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:182769980 G>A maps to NM_020166.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr3:195608973 G>A maps to NM_001010938.1 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:844869 G>A maps to NM_005255.2 Q1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:5961299 G>A maps to ENST00000324058 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:6843852 G>A maps to NM_014743.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr4:39512008 G>C maps to NM_003359.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:14399068 C>T maps to NM_007118.2 R1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:98209410 G>A maps to NM_001270.2 R1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:140552991 C>G maps to NM_018940.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:140553378 C>T maps to NM_018940.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:140751512 C>T maps to NM_018924.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:149677552 G>A maps to NM_001012301.2 R312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr5:171765984 G>A maps to NM_001017995.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:2683269 G>C maps to NM_001012418.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:27101101 C>A maps to NM_021064.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:29797698 G>A maps to ENST00000376828 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:131923476 G>T maps to ENST00000403834 S665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:153073416 C>T maps to NM_003381.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:160663434 C>G did not map to a codon.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr6:167352456 C>T maps to ENST00000428859 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:17382604 C>T maps to NM_001621.4 Q822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:45016618 C>T maps to NM_033054.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr7:99796486 G>A maps to NM_012447.2 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:28974497 G>A maps to NM_015254.3 S1229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:67040612 T>C maps to NM_184085.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:70744344 G>A maps to NM_030958.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:98718972 C>T maps to NM_178812.3 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:110495273 C>G maps to ENST00000426474 L3172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr8:141549522 C>A maps to NM_012154.3 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:17457538 G>A maps to NM_017738.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:87338521 C>T maps to NM_006180.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:103312380 A>T maps to NM_001198812.1 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chr9:133759971 G>A maps to NM_007313.2 K784K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:15818000 C>G maps to NM_005089.3 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:16707721 G>A maps to NM_001144002.1 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:19764520 G>A maps to NM_031892.2 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:32328261 G>C maps to ENST00000357033 L2018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:48214124 G>C maps to NM_021014.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:78010590 T>A maps to NM_005296.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:105970541 T>C maps to NM_194463.1 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:118284332 T>C maps to NM_020721.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:119670882 G>A maps to NM_003588.3 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:152821835 G>A maps to NM_001001344.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OP-01A-21D-A21Z-08 chrX:153224214 C>A maps to ENST00000369984 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:6188916 G>C maps to NM_015557.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:19491417 C>T maps to ENST00000375267 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:152282757 G>C maps to NM_002016.1 S1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr1:156131201 C>G maps to NM_022367.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr11:3147783 C>T maps to NM_020896.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr12:132624236 C>T maps to NM_175066.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:32563174 A>G maps to NM_001030055.1 K1100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:50360894 G>A maps to NM_001663.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr14:78023406 G>A maps to NM_004863.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr15:34648552 G>T maps to ENST00000438749 E772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr17:33903109 G>A maps to NM_000286.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:1487827 G>A maps to NM_017573.3 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:53056855 A>G maps to NM_001039886.3 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:53770825 G>A maps to NM_173857.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr19:58265940 T>C maps to NM_173632.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr2:96906234 T>A maps to NM_001037228.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr2:233710440 G>A did not map to a codon.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr3:131220432 T>C maps to ENST00000425847 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr4:54248501 G>A maps to NM_030917.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr4:151357946 G>A maps to NM_006726.3 Q2295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr5:10981932 C>T maps to NM_001332.2 L1123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr5:140214243 C>G maps to NM_018910.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr5:140228355 C>G maps to NM_031857.1 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr6:33694646 G>C maps to NM_054111.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr7:94163032 C>T maps to NM_022900.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr7:148768419 G>A maps to NM_152411.3 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr8:17422583 C>T maps to NM_001164771.1 Q676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr8:27145408 G>A maps to NM_171982.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr8:36766905 G>A maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chr9:117002528 C>T maps to NM_032888.2 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OQ-01A-32D-A21Z-08 chrX:14882864 G>A maps to NM_152633.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr1:101490987 G>A maps to NM_015958.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr1:145601613 G>A maps to NM_006468.6 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr1:248737332 G>C maps to NM_001001821.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr10:74690367 C>T maps to NM_152635.1 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr10:128925982 C>T maps to ENST00000398025 T913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr11:44146518 C>G maps to NM_000401.3 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr12:46318786 C>T maps to NM_004719.2 P1210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr12:124104078 C>T maps to NM_020936.1 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr14:33291374 C>T maps to NM_004274.4 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr16:1706029 G>T maps to NM_020825.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr16:81173268 G>A maps to NM_052892.3 I1822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:7193037 G>A maps to NM_015982.3 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:35300097 G>A maps to NM_005568.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:73055694 G>T maps to NM_015353.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr17:78444648 G>T maps to NM_002522.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr19:3151743 C>T maps to NM_002068.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr2:32640935 C>G maps to NM_016252.3 L859L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr2:179404370 G>A maps to NM_133378.4 D30239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr3:122354757 C>A maps to NM_001113523.1 Y616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr3:164697152 T>A maps to NM_001041.3 S1827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr4:10079466 G>A maps to NM_017491.3 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr4:94344055 C>T maps to NM_001510.2 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr5:110784839 C>G maps to NM_001744.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr6:12120591 C>T maps to NM_002114.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr6:45917027 G>T maps to NM_001114086.1 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr6:147648377 C>T maps to NM_001127715.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr7:8110598 C>A maps to NM_138426.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr7:97862829 C>G maps to ENST00000379795 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr8:108972968 A>G maps to NM_178565.4 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr8:145057979 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr9:90262308 G>T maps to NM_004938.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chr9:91926142 C>T did not map to a codon.
Sequencing variant TCGA-GD-A3OS-01A-12D-A21Z-08 chrX:103359014 C>T maps to NM_001143978.1 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:11596631 C>T maps to NM_020780.1 F1356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:22902807 G>A maps to NM_020526.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:27100987 C>T maps to NM_006015.4 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:46745287 T>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:100701033 G>C maps to NM_001918.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:155154487 C>T maps to NM_025058.3 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:155922417 C>A did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:196965185 C>A maps to ENST00000367414 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr1:202936372 G>C did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr10:76993950 C>T maps to NM_144589.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr10:119013595 T>C maps to NM_003054.4 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:3704661 C>T maps to NM_016320.4 E1562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:10022459 C>T did not map to a codon.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:62763285 G>C maps to ENST00000430500 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr11:64571829 G>C maps to NM_130804.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:21608983 G>A maps to NM_024854.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:48547242 G>A maps to NM_024095.3 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:48736908 C>T maps to NM_152320.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:53045869 G>A maps to NM_000423.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:73012709 C>T maps to NM_013381.2 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr12:100797868 T>C maps to NM_139319.2 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:32912513 C>G maps to NM_000059.3 S1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:49933857 G>A maps to NM_001079670.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:70681660 G>C maps to NM_020866.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:72146981 G>C maps to ENST00000359684 S484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr13:88329085 G>A maps to NM_015567.1 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr14:39717073 T>C maps to NM_054024.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr15:28231759 C>T maps to NM_000275.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr15:75122673 T>C maps to NM_001030005.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr15:89760378 G>A maps to NM_000326.4 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr16:30995214 G>A maps to NM_014712.1 K1665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr16:87921737 G>A maps to NM_001739.1 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:3432258 G>A maps to ENST00000381913 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:10231293 A>G maps to NM_003802.2 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:34094868 G>C maps to NM_024302.3 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:40379651 G>C maps to NM_012448.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:76866986 G>A maps to NM_003255.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr17:79891200 C>T maps to ENST00000432920 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:16045053 C>T maps to NM_021187.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:16982109 C>T maps to NM_015260.1 I863I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:34949726 A>G maps to NM_005499.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr19:46998593 G>A maps to NM_020709.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:21233835 G>A maps to NM_000384.2 V1968V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:37873445 G>A maps to NM_006449.3 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:42990227 G>A maps to NM_148962.4 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:48808502 C>A maps to NM_172311.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:64114601 G>T maps to NM_006759.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:172016854 C>T maps to ENST00000360843 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:189876409 G>C maps to NM_000090.3 V1437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr2:241421609 C>A maps to ENST00000401804 E959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr21:30307607 T>C maps to NM_015565.2 S1612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr22:19504099 G>A maps to NM_001178010.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr22:19951737 G>A maps to NM_001135162.1 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr22:46319095 C>T maps to NM_058238.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr3:44943288 G>C maps to NM_003241.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr3:47147507 G>A maps to NM_014159.6 F1606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr3:100463741 C>T maps to NM_001007565.2 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr4:1806111 C>T maps to NM_000142.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr4:170038902 G>A maps to NM_020870.3 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:37173928 G>A maps to NM_023073.3 F2033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:37816163 C>T maps to NM_001190468.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:43628316 A>G maps to NM_182977.2 E264E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:54640369 A>G maps to NM_015360.4 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:125967494 C>G maps to NM_207408.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr5:179151699 C>T maps to ENST00000415618 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr6:109471319 G>C did not map to a codon.
Alternatively spliced codon TCGA-GU-A42R-01A-11D-A23M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:91603050 T>C maps to NM_005751.4 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:107335097 G>T maps to NM_000441.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:128470903 C>T maps to NM_001458.4 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:150767331 C>T maps to NM_003040.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr7:151791434 C>T maps to NM_022087.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr8:22052269 C>T maps to NM_006129.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr8:109240614 C>G maps to NM_001568.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr8:133047064 C>T maps to ENST00000262283 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr9:37746351 G>A maps to NM_014907.2 G1441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr9:99381612 G>C maps to NM_033331.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chr9:116854868 G>A maps to ENST00000259410 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chrX:44966675 G>A maps to NM_021140.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chrX:48925200 C>T maps to ENST00000422185 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chrX:70351452 C>T maps to ENST00000333646 I1367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GU-A42R-01A-11D-A23M-08 chrX:73812255 T>C maps to NM_183353.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr1:27100374 C>T maps to NM_006015.4 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr1:228005155 G>A maps to NM_183062.2 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr10:120925083 C>A maps to NM_213649.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr11:617953 C>T maps to NM_021924.4 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr11:65123926 C>T maps to NM_145719.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr11:67077776 G>A maps to NM_017857.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr12:11000980 G>A maps to NM_007244.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr12:78360076 T>C maps to NM_014903.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr13:33635873 G>A maps to NM_004795.3 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr14:95688090 C>T maps to NM_024734.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr15:78790397 C>T maps to NM_004136.2 S935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr16:2818181 G>C maps to NM_016333.3 S2551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr16:3779152 C>T maps to NM_004380.2 E1965E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr17:1028676 G>A maps to NM_021962.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr18:19154690 T>C maps to NM_052911.2 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr19:8576364 C>T maps to NM_032370.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr19:8665901 G>A maps to NM_030957.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr2:1497622 C>T maps to NM_000547.5 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr20:126331 G>A maps to NM_030931.2 *112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr20:37117125 C>T maps to NM_020336.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr20:43572201 G>A maps to NM_006809.4 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr22:28193513 C>T maps to NM_002430.2 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:11058950 C>T maps to NM_003042.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:13376965 C>T maps to NM_024923.2 E1277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:13377028 C>T maps to NM_024923.2 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:61989041 C>T maps to NM_002841.3 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:68466475 G>A maps to NM_213609.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr3:119445048 G>A maps to NM_033364.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:5837698 G>A maps to NM_001014809.1 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:38016440 G>A maps to NM_015173.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:48549696 G>A maps to NM_015030.1 R1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr4:186545478 G>A maps to ENST00000355634 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:484633 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:1232400 C>T maps to NM_182632.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr5:140719539 C>T maps to NM_018915.2 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:33245983 C>A maps to NM_003782.3 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:71234833 C>T maps to NM_001162529.1 R683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:151055092 A>G maps to NM_001029884.1 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:158564167 G>A maps to NM_032861.3 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr6:162864341 C>T maps to NM_004562.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr7:72850004 C>T maps to NM_003508.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr7:148768942 T>C maps to NM_152411.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr8:117950662 C>T maps to NM_001025357.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chr8:125082840 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JV-01A-11D-A21Z-08 chrX:52844173 C>T maps to NM_130775.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr1:57373627 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr10:121663629 G>A maps to NM_007190.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr13:42876627 C>G maps to NM_016248.2 S1249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr14:24731537 G>A maps to NM_000359.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr14:70418940 C>A maps to NM_001034852.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr14:70991612 G>A maps to NM_003814.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:24268125 C>T maps to NM_006539.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:29883847 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr16:30545883 G>A maps to NM_023931.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:4718856 G>A maps to NM_002663.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:18155373 C>T maps to NM_002018.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:33769021 C>T maps to NM_144682.5 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:48155573 G>A maps to NM_002204.2 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:65941561 G>A maps to ENST00000321892 Q2372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr17:80333363 G>A maps to NM_018949.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr18:8624997 T>C did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr19:18778893 G>A maps to NM_018316.1 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr19:53644379 T>C maps to NM_001172674.1 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr19:58639721 G>A maps to NM_024620.3 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr2:103013324 G>A maps to NM_003855.2 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr2:108994730 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr3:5249806 C>T maps to NM_014674.2 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr3:33870427 G>A maps to NM_001162429.1 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr3:195512117 G>A maps to NM_018406.5 T2111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr4:79832994 C>T maps to NM_198892.1 V1098V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr5:112769744 G>A maps to NM_032028.3 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr5:140784366 C>T maps to NM_018921.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr6:18122764 C>A maps to NM_198586.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr7:99308459 A>C maps to ENST00000292414 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr9:130207139 A>G maps to NM_007135.2 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JW-01A-11D-A20D-08 chr9:131397987 C>A maps to NM_052844.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:3544177 G>A maps to NM_182752.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:6196892 G>C maps to NM_015557.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:19653761 C>T maps to NM_017765.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:23767921 G>A maps to NM_017707.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:38265847 C>T maps to NM_001113482.1 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:110050082 C>T maps to NM_020703.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:117633951 C>G maps to NM_003594.3 S864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:152770488 G>A maps to NM_178352.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:152770613 G>A maps to NM_178352.2 *115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:159897218 G>A maps to NM_001135050.1 F1152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:169825054 C>T maps to NM_181093.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:203676347 G>A maps to NM_001001396.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:207112587 C>T maps to NM_002644.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:212911827 C>T maps to NM_015471.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr1:220174522 G>T maps to NM_004446.2 S713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr10:18840785 G>T maps to NM_182543.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr10:75849104 C>T maps to NM_014000.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr10:102056961 C>T maps to NM_016112.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr11:61507076 C>T maps to NM_006133.2 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr11:118485344 C>T maps to NM_015157.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:53676184 C>G maps to NM_012291.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:85266413 G>C maps to NM_182767.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:94543415 C>G maps to NM_005761.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:104487162 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr12:110002928 G>A maps to NM_052845.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:48934193 C>T maps to NM_000321.2 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:53039468 C>T maps to NM_001098525.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:96246296 T>C maps to NM_198968.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr13:114523971 C>T maps to ENST00000357389 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:56142554 G>A maps to NM_001079521.1 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:58954656 T>G maps to ENST00000354386 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:74567921 T>C maps to NM_001024674.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:74825045 G>C maps to NM_018228.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr14:102718330 C>G maps to NM_014226.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr15:65702610 C>T maps to NM_020962.1 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr15:75183865 C>T maps to NM_002435.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:700001 G>A maps to NM_145294.4 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:3820784 G>C maps to NM_004380.2 S889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:20552066 G>T maps to NM_182617.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:30616004 G>C maps to NM_138447.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr16:83704468 C>T maps to ENST00000268613 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:1370775 G>A maps to NM_001080779.1 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:33430493 G>A maps to NM_002878.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:47699429 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:72368384 G>A maps to ENST00000440684 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr17:73231772 G>A maps to NM_024844.3 *657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:2921614 G>A maps to NM_014646.2 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:5489113 C>A maps to NM_012307.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:9570581 C>T maps to NM_001042388.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:12367071 G>C maps to NM_006796.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr18:14764039 T>C maps to NM_001145029.1 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:4511892 C>G maps to NM_001080400.1 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:4944247 C>G maps to ENST00000398240 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:6732094 C>T maps to NM_001080452.1 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:31039135 G>A maps to NM_014717.1 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:41737166 G>C maps to NM_021913.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:45805791 C>T maps to ENST00000262891 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr19:52994575 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:96048222 C>T maps to NM_013434.4 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:113940992 C>T maps to NM_012455.2 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:160833208 G>A maps to NM_007366.4 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:160840458 G>C maps to NM_007366.4 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:169681197 G>A maps to NM_001171631.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:179319143 C>T maps to NM_001042702.3 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr2:219508868 C>T maps to NM_001105537.1 E790E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr20:61512798 C>T maps to NM_033081.2 Q1503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr20:62038152 G>C maps to NM_172107.2 Y821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr21:43838514 G>A maps to NM_018961.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr22:36695027 C>A maps to NM_002473.4 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:10254973 C>G maps to NM_001570.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:13381431 G>A maps to NM_024923.2 L1131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:16475482 G>A maps to NM_015150.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:38988356 G>A maps to ENST00000302328 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:52859943 G>A maps to ENST00000485816 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr3:128973916 C>T maps to NM_016128.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:7398028 G>C maps to NM_020777.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:143045827 C>G maps to NM_003866.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:169108569 T>C maps to NM_007193.3 D320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr4:178274822 G>A maps to NM_018248.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:169622 C>T maps to NM_052909.3 H859H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:50685564 G>C maps to NM_002202.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:140750462 C>T maps to NM_018924.2 Q168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:150925436 C>A maps to NM_001447.2 E1751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr5:178977722 G>A maps to NM_025158.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr6:32156276 G>A maps to NM_002586.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr6:111697610 G>A maps to NM_002912.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr7:84671601 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr8:59522182 G>A maps to NM_001144772.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:128677987 G>T maps to ENST00000373487 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:131348069 G>A maps to NM_001130438.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:131348090 G>A maps to NM_001130438.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chr9:136917463 G>A maps to NM_007371.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chrX:129149372 C>G maps to ENST00000303743 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chrX:129149589 C>T maps to ENST00000303743 Q948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JX-01A-11D-A20D-08 chrX:150911829 C>A maps to NM_005140.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:1268135 C>T maps to NM_152228.1 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:2125220 C>T maps to ENST00000359030 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:11132176 C>A maps to NM_001001998.1 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:25599109 C>T maps to ENST00000357542 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:43637292 G>A maps to NM_001159936.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:75037068 G>C maps to NM_001002912.4 S1442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:115147613 C>T maps to ENST00000393274 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:118624182 T>C maps to NM_206996.2 K615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:144857624 G>A maps to NM_014644.4 I2143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:144882661 G>C maps to NM_014644.4 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:151065681 G>T maps to NM_144618.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:152191809 G>A maps to NM_001009931.1 H765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:155234439 G>A maps to ENST00000368361 I353I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:155630384 G>T maps to ENST00000368339 S577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:155891201 C>T maps to NM_014949.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:156230256 G>C maps to NM_015327.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:156698907 C>T maps to NM_015997.3 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:158747167 G>A maps to NM_001005278.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:159161792 G>A maps to NM_021189.3 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:159161861 G>A maps to NM_021189.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:167096653 C>A maps to NM_001080426.1 C762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:181019243 G>C maps to NM_001531.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:193028360 G>A maps to ENST00000367450 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:197398671 G>T maps to NM_201253.2 E924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:216850700 G>A maps to NM_001438.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:230415080 G>C maps to NM_004481.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:235383126 C>A maps to NM_016374.5 E522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr1:235611709 C>G maps to NM_003193.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:3155562 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:15326104 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:27437903 G>A maps to NM_139312.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:27437956 G>A maps to NM_139312.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:28897141 C>G maps to NM_016628.3 S316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:34805960 G>A maps to NM_019619.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:55569090 G>A maps to NM_001142769.1 R1578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr10:119014791 C>A maps to NM_003054.4 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:4616238 C>G maps to ENST00000450052 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:17172071 G>A maps to NM_002645.2 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:51412329 T>C maps to NM_001005272.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:59271356 C>T maps to NM_001004706.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:62293740 C>T maps to NM_001620.1 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:76506761 C>T maps to NM_015516.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:89424090 C>A maps to NM_153696.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr11:130275533 G>A maps to NM_007037.4 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:49447269 G>A maps to NM_003482.3 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51118559 C>T maps to NM_173602.2 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51585470 G>A maps to NM_002702.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51586128 G>A maps to NM_002702.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:51586206 G>A maps to NM_002702.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:54686941 G>C maps to NM_001136023.1 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr12:123338614 C>T maps to NM_003959.1 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr13:113814359 C>T maps to ENST00000342783 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr13:114503879 C>T maps to NM_182614.2 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:24606975 G>A maps to NM_176783.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:24727512 G>A maps to NM_000359.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:32560833 C>G maps to NM_001030055.1 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:52477649 G>A maps to NM_007361.3 V1222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:77492328 G>A maps to NM_024496.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:78397943 C>G maps to NM_020421.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:105242099 G>A maps to NM_001014432.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr14:105419486 C>T maps to NM_138420.2 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr15:31619855 C>G maps to NM_015995.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr15:62254673 C>A maps to NM_020821.2 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr15:67477080 C>G maps to NM_005902.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:677450 C>T maps to NM_021168.4 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:2237254 C>A maps to NM_020764.3 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:23724502 C>T maps to NM_033266.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:28145185 C>T maps to NM_015171.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:30776274 C>G maps to NM_014771.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:55363209 G>C maps to NM_024335.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69368865 G>C maps to NM_032382.4 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69370434 C>T maps to NM_032382.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:69373449 C>T maps to NM_032382.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr16:89352492 G>A maps to NM_013275.4 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:4876990 C>T maps to NM_015099.3 W697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:7330188 C>T maps to NM_175734.4 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:8048195 C>G maps to NM_002616.2 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:61678639 C>T maps to NM_016360.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:71391399 G>A maps to NM_001144952.1 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:78449359 G>T maps to NM_002522.3 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr17:79287596 G>A maps to NM_178520.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:22806744 C>T maps to NM_015461.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:23612473 A>T maps to ENST00000415083 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:47101863 C>T maps to NM_006033.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:47777949 C>G maps to NM_145020.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr18:67992251 G>A maps to NM_004232.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:7964520 C>T maps to NM_025061.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:7992541 C>T maps to NM_006351.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:12767435 G>A maps to NM_000528.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:15164701 G>T maps to NM_012114.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:30934885 C>T maps to NM_014717.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:34884964 C>T maps to NM_000175.3 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:38633218 C>T maps to NM_015073.1 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:40580581 C>T maps to NM_001142577.1 E590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:41351240 T>C maps to NM_000762.5 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:42796293 G>C maps to NM_015125.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:46178077 G>A maps to NM_000164.2 W209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr19:52785368 C>T maps to NM_001010851.2 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:20251206 G>C maps to NM_014713.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:20251239 G>A maps to NM_014713.4 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:25990550 G>A maps to NM_018263.4 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:27260563 G>A maps to NM_017727.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:37366872 C>T maps to NM_001135651.1 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:48573385 G>A maps to NM_002158.3 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:55523008 G>A maps to ENST00000436346 R1759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:65217169 C>T maps to NM_003038.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:71730409 C>T maps to NM_001130987.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:152468804 C>G maps to NM_001164507.1 L3900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:201469495 G>T maps to NM_001159.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr2:234386115 G>A maps to NM_018218.2 I1222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:33364228 C>T maps to NM_014071.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:33891824 C>T maps to NM_018244.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:42694695 C>A maps to ENST00000348077 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr20:60921966 A>C did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr21:35468010 C>T maps to NM_006933.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr21:46876058 C>G maps to ENST00000359759 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr22:29738342 C>T maps to NM_001127.3 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr22:30185084 C>A maps to NM_032204.3 E731*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GV-A3JZ-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-GV-A3JZ-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:19975087 C>A maps to NM_144715.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:53905382 C>A maps to NM_022899.4 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:58631353 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:74344387 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:101038511 G>A maps to NM_016247.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:105421028 G>C maps to NM_170662.3 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:121509012 C>A maps to NM_001023570.2 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:121642097 G>A maps to NM_021082.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:142682016 G>A maps to NM_198504.2 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:169539843 C>T maps to NM_001080460.1 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:179371084 C>T maps to NM_003940.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr3:184099749 C>G maps to NM_003741.2 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:4199381 G>A maps to NM_177998.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:38138895 G>A maps to NM_015173.2 R1149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:40104487 G>A maps to NM_018177.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:62849138 C>T maps to ENST00000506720 F1018F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:90857266 T>C maps to NM_007351.2 D812D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr4:119951528 G>A maps to NM_133477.2 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:38947494 C>T maps to ENST00000296782 L1419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:71494798 C>T maps to NM_005909.3 Q1873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:140563915 C>T maps to NM_020957.1 G594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:142435651 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:170319553 C>G maps to NM_022897.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr5:170610194 G>A maps to NM_022897.3 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:7727602 C>T maps to NM_001718.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:7727749 C>T maps to NM_001718.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:7891865 G>A maps to NM_030810.3 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:26184244 C>T maps to NM_003523.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:36982666 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:53516581 C>T maps to NM_001003760.4 W573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:74119056 G>A maps to NM_018665.2 Q422Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:136882783 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:150174189 G>A maps to NM_032832.5 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr6:152737831 G>A maps to NM_182961.2 Q1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:21840769 C>T maps to NM_003777.3 L3355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:33066464 G>A maps to NM_001002010.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:39500144 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:82997264 C>T maps to NM_012431.2 Q655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:87757966 G>C maps to NM_021723.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:92158135 G>A maps to NM_032120.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:98534848 G>A maps to ENST00000359863 L1394L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GV-A3JZ-01A-11D-A21A-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:100363104 C>T maps to ENST00000349350 F1466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:123092842 G>C maps to NM_178827.4 S777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:127978388 C>T maps to NM_018077.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr7:144097328 C>T maps to ENST00000467773 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr8:42611279 C>T maps to NM_004198.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr8:53084385 G>A maps to NM_014682.2 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr8:144940344 C>T maps to NM_031308.1 V2359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:33466614 C>T maps to NM_022917.4 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:36246415 C>G maps to NM_001128227.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:115806038 G>A maps to NM_003408.1 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:119461343 G>A maps to NM_012210.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:124535707 G>A maps to ENST00000408936 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:130265176 G>A maps to NM_001005374.2 *724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:136531910 G>A maps to NM_007101.3 F859F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chr9:139887393 G>C maps to NM_183241.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chrX:46434157 G>A maps to NM_019886.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3JZ-01A-11D-A21A-08 chrX:103267743 G>C maps to NM_001002916.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr1:37271788 C>A maps to NM_000831.3 E744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr1:84944969 G>T maps to NM_025065.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr1:93300334 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr10:18292238 C>A maps to NM_001145195.1 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:5410828 G>T maps to NM_001004756.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:20178182 C>T maps to ENST00000227256 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:55681671 G>T maps to NM_001001960.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:64494817 C>A maps to ENST00000320253 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr11:65392688 T>C maps to NM_032223.2 C989C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr12:117914393 C>T maps to ENST00000339824 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr12:122818657 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr12:124359911 G>A maps to NM_207437.3 K2573K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr14:20249176 T>A maps to NM_001005500.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:2813315 C>T maps to NM_016333.3 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:7645612 C>T maps to NM_145891.2 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:46638000 G>T maps to NM_024745.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr16:58620580 G>A maps to NM_016284.3 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr17:59821937 T>C maps to NM_032043.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr18:12794330 A>T maps to NM_002828.2 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr18:54694284 G>A maps to NM_015285.2 Q1440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr18:74980671 C>T maps to NM_001480.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:8161816 G>A maps to NM_032447.3 Y1787Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:31769795 T>C maps to NM_020856.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:42583135 C>G maps to ENST00000222339 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr19:51171700 G>A maps to ENST00000391814 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:1652947 C>T maps to NM_012293.1 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:71894599 G>A maps to NM_001130987.1 V1804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:101670702 G>A maps to NM_001102426.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:179644784 A>T maps to NM_133378.4 L1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:179644786 G>T maps to NM_133378.4 A1223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:197889931 T>A maps to NM_001195144.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr2:210559446 T>C maps to NM_002374.3 T851T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr20:32349814 G>A maps to ENST00000375200 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr21:45542226 G>A maps to NM_005049.2 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr3:127379998 G>A maps to NM_015720.2 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr3:138474749 T>C maps to NM_006219.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr5:70761988 A>G maps to NM_018429.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr6:29012934 A>G maps to NM_030903.3 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr6:41712174 G>A maps to NM_002630.3 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr6:151907136 G>A maps to ENST00000367290 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr7:31683173 C>T maps to NM_194300.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr7:45726144 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr7:88963714 T>C maps to NM_181646.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:2824090 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:110131362 C>T maps to NM_003301.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:110439237 C>T maps to ENST00000426474 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr8:120428804 C>T maps to NM_002514.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:429742 C>T maps to NM_203447.3 F1505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:34622476 T>C maps to NM_001017363.1 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:135777086 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chr9:139276291 G>A maps to NM_003086.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chrX:44922801 C>T maps to NM_021140.2 Q555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QF-01A-31D-A22Z-08 chrX:53106252 G>A maps to NM_018969.5 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr1:214814729 C>T maps to NM_016343.3 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr1:247614708 C>T maps to NM_001004492.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr1:248005057 G>A maps to NM_001001959.1 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr10:28908492 G>A maps to NM_016628.3 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr10:30915166 G>A maps to NM_183058.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr10:87487629 G>T maps to NM_017551.2 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr11:66297374 G>A maps to NM_024649.4 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr12:124846734 G>A maps to NM_006312.4 Q1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr15:83876118 G>A maps to NM_016073.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr16:56920341 C>G maps to NM_000339.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr17:1939320 G>T maps to NM_001383.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:5727328 C>A maps to NM_152784.3 C59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:46180988 C>G maps to NM_000164.2 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:48601510 C>T maps to NM_003706.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr19:49316805 G>A maps to NM_016246.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr2:100209851 T>C maps to NM_001025108.1 L782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr2:109379690 A>G did not map to a codon.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr20:1460372 C>T maps to NM_001122962.1 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr22:31486842 C>T maps to ENST00000454496 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr22:40161510 G>A maps to NM_152512.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr3:18427953 C>T maps to ENST00000332610 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr4:114286339 T>G did not map to a codon.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr4:155191120 G>A maps to NM_017639.3 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr6:17601038 C>T maps to NM_016255.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr6:53989533 C>A maps to ENST00000502396 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr6:109484116 C>T maps to NM_173830.4 R443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chr8:42045070 G>A maps to NM_000930.3 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QG-01A-11D-A21Z-08 chrX:12736409 C>T maps to ENST00000429478 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr1:116941292 G>A maps to NM_000701.7 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr10:15760898 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr10:115401141 A>G maps to ENST00000369358 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:1268536 C>A maps to ENST00000447027 S3479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:2975839 C>A maps to ENST00000399624 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:3380677 C>T maps to NM_001130520.1 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:18322408 C>T maps to NM_181507.1 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:48267008 C>T maps to NM_001004727.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:61039179 C>T maps to NM_152718.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:62397102 G>C maps to NM_198335.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:65547045 T>C maps to NM_138368.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:66360120 C>T maps to NM_018219.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:92616245 G>A maps to ENST00000298047 P4208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr11:119061143 G>C maps to NM_001145018.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr12:83081400 C>T maps to NM_152588.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr14:23596403 C>T maps to NM_012244.2 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr14:72196848 G>A maps to NM_015556.1 S1585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr15:66015200 G>A maps to ENST00000443035 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr15:69677201 C>T maps to NM_017705.3 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr16:46771855 C>T maps to NM_182493.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr16:64981661 A>C maps to NM_001797.2 Y745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr16:89735692 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:34077314 C>T maps to NM_139285.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:35615270 T>G maps to NM_198834.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:37868199 C>T maps to NM_004448.2 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr17:66899518 G>A maps to NM_007168.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr18:30804900 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr18:56816746 C>T maps to NM_033280.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr18:60241917 C>T maps to NM_017742.4 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:1231041 C>A maps to NM_152769.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:41782118 C>T maps to NM_007040.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr19:57133449 C>G maps to NM_021216.4 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr2:179411949 G>A maps to NM_133378.4 H28866H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr2:179582432 G>A maps to NM_133378.4 Q7146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr20:25656895 G>C maps to NM_015655.2 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr20:33364213 C>T maps to NM_014071.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr20:34526617 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr21:45479021 C>T maps to NM_003274.4 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr22:17976512 G>C maps to ENST00000400579 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr22:44532338 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr3:142840194 C>T maps to NM_004267.3 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr3:161221323 C>A maps to NM_001080440.1 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr4:26675452 C>T maps to NM_018317.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr4:187004825 C>T maps to NM_003265.2 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:7773124 C>T maps to NM_020546.2 I765I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:52351968 C>T maps to NM_002203.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:58021939 C>T maps to NM_138453.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:122881388 C>G maps to NM_001044723.1 S11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:140569144 G>A maps to NM_019119.3 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:140569219 C>T maps to NM_019119.3 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:140793095 G>A maps to NM_018913.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr5:179201772 G>T maps to NM_014757.4 G982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:43011252 G>A maps to NM_001168370.1 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:73110199 G>C maps to NM_014989.4 V1621V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:97561858 C>T maps to NM_052904.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr6:160239601 C>T maps to NM_173516.1 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:24745980 G>T maps to NM_001127453.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:28319233 A>C did not map to a codon.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:50468279 C>T maps to NM_006060.3 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:50660678 G>C maps to NM_005311.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:70255919 C>T maps to NM_015570.2 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:72193852 G>A maps to NM_001145440.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:124404067 G>A maps to NM_005302.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr7:140159648 G>C maps to NM_013446.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr8:11995858 G>A maps to NM_201402.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr8:68150722 C>T maps to NM_006421.3 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr9:71844152 G>T maps to NM_004817.3 E503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chr9:132590499 G>A maps to NM_016520.2 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chrX:10093066 C>T maps to NM_015691.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chrX:152815031 C>T maps to NM_001001344.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QH-01A-11D-A21Z-08 chrY:15466933 C>T maps to NM_007125.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:1374719 G>T maps to NM_022834.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:39800780 G>T maps to ENST00000289893 E1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:54670970 G>A maps to NM_016491.3 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:144864172 G>A maps to NM_014644.4 F1974F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:144877096 G>A maps to NM_014644.4 F1530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:146399627 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:153998044 G>A maps to NM_207308.2 V1365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:156640229 C>T maps to NM_006617.1 Q1250Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:158747266 T>C maps to NM_001005278.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:159166684 C>T maps to NM_021189.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:159683377 G>A maps to NM_000567.2 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:175086216 G>A maps to NM_022093.1 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:204170900 C>T maps to NM_198447.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:205561359 C>T maps to NM_181644.4 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:206566185 C>T maps to ENST00000414359 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:235964227 C>T maps to NM_000081.2 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr1:240072202 C>G maps to NM_000740.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:13481366 G>A maps to ENST00000396900 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:33211202 C>T maps to ENST00000374956 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:50820267 C>T maps to NM_003055.2 Y494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:70206089 C>T maps to NM_001080449.1 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:82269118 G>A maps to NM_030927.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:112650397 G>C maps to NM_014456.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr10:124357508 C>G maps to ENST00000368915 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:11987390 G>T maps to ENST00000450094 C265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:18434293 G>A maps to NM_017448.3 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:20940865 A>T maps to NM_006157.3 K249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:32781667 A>T maps to NM_001008391.2 L41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:33370304 C>T maps to NM_005734.3 V869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:40136114 C>A maps to NM_020929.1 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:44255774 G>T maps to NM_000401.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:46802035 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:56185024 G>A maps to NM_001004744.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:62292549 C>A maps to NM_001620.1 L3113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:70277331 G>C maps to NM_001184740.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:88780575 G>T maps to NM_001143831.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:94597965 C>T maps to NM_130847.2 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:108175523 T>C maps to NM_000051.3 C1873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:124310917 C>A maps to NM_012378.1 G22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr11:124440002 C>T maps to NM_001005194.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:6882427 C>A maps to NM_002286.5 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:20886038 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:48191919 G>C maps to NM_015401.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:48739258 T>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:50189720 G>T maps to NM_001037806.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:90004245 G>A maps to ENST00000428670 R763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:100048913 T>A maps to NM_152788.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:110290443 G>C maps to NM_016433.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:117724010 A>G maps to ENST00000338101 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:120195198 C>T maps to ENST00000392521 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:124403342 C>T maps to NM_207437.3 L3667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr12:132241140 A>T maps to NM_004592.2 K558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:24738748 G>A maps to NM_182836.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:24800295 G>A maps to NM_139247.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:29237879 G>A maps to NM_005249.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:61486257 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:64153044 C>A maps to NM_030791.2 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:67940531 A>G maps to NM_182526.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr14:94404062 G>C maps to ENST00000434324 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:34640692 A>G maps to ENST00000438749 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:45713303 C>T maps to NM_024063.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:69677080 G>A maps to NM_017705.3 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr15:79748438 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:20380852 G>A maps to NM_174924.1 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:28947483 G>C maps to NM_001178098.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:31090893 C>T maps to NM_014699.3 V1083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr16:77896682 C>T maps to NM_020927.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:3100985 C>T maps to NM_012352.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:4797303 C>T maps to NM_153827.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:6674104 A>T maps to NM_017523.2 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:18513401 C>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:35454053 C>G maps to NM_198834.1 L2256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:76554222 G>A maps to ENST00000389840 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr17:78179328 G>C did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:2688389 A>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:8784102 G>T maps to ENST00000456698 G691G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:67788893 C>T maps to NM_173630.3 L1142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:72999302 G>A maps to NM_005786.4 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr18:74580690 G>A maps to NM_007345.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:2216761 G>A maps to ENST00000221482 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:4361710 G>A maps to NM_003025.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:4504532 G>A maps to NM_001080400.1 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:9086870 G>T maps to NM_024690.2 A1648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:10116260 G>A maps to NM_015719.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:11558506 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:12984212 G>T maps to NM_014975.2 S1113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:13325351 G>T maps to NM_023035.2 S1938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:14640522 G>A maps to NM_138501.4 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:40354439 C>T maps to NM_003890.2 K5343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:42092191 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:50393823 C>A maps to NM_172374.1 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:51140566 C>T maps to NM_001160329.1 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:54848848 C>T maps to NM_012276.3 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr19:58265856 C>T maps to NM_173632.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:27821095 G>A maps to NM_032434.2 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:61416072 C>T maps to NM_014709.3 E3335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:77745524 A>T maps to NM_001134745.1 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:77746265 G>A maps to NM_001134745.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:88405959 C>A maps to NM_198274.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:98996643 G>A maps to NM_001298.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:121747230 T>C maps to NM_005270.4 Y1247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:130872848 G>A maps to NM_001099771.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:152330583 C>G maps to NM_018151.4 S2401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:163213344 C>T maps to NM_012198.3 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:166246147 C>A maps to NM_001040142.1 P1944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr2:198367981 G>A maps to NM_002157.2 *103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:3730478 C>T maps to NM_052970.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:34057720 C>G maps to NM_007186.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:43115336 A>T maps to NM_024331.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr20:52788148 C>A maps to NM_000782.4 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr21:45994246 C>T maps to NM_198687.1 C204C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:17073278 G>A maps to NM_014406.4 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:38119891 C>G maps to NM_001039141.2 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:38120038 C>G maps to NM_001039141.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:41257776 G>A maps to NM_145174.1 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr22:44031096 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:69113225 G>A maps to NM_003968.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:112059795 G>A maps to NM_001004196.2 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:113188078 G>C maps to NM_144718.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:113376933 G>A maps to NM_001009899.2 Q1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:121410944 C>T maps to ENST00000393667 L2422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:126142416 C>T maps to ENST00000505024 Q407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:127391915 C>T maps to NM_172027.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:136085924 C>G did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:138724663 G>A maps to NM_001134659.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:141497287 G>A maps to NM_139209.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:142681983 A>T maps to NM_198504.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr3:171427486 T>C maps to NM_002662.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:3424263 G>A maps to NM_198229.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:3449272 G>A maps to ENST00000511533 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:62800643 G>T maps to ENST00000506720 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:82355882 C>T maps to NM_152545.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:87080491 C>T maps to NM_138982.2 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:175898027 C>G maps to NM_014269.4 S451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr4:184367944 C>T maps to NM_017632.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:13753589 G>A maps to NM_001369.2 L3542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:127674744 C>A maps to NM_001999.3 E1118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:140209922 G>A maps to NM_018909.2 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:140255206 G>A maps to NM_018903.2 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr5:140573672 C>T maps to NM_018930.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:34003489 C>A maps to NM_000841.1 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:35586901 G>C maps to NM_001145775.1 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:41010862 T>C maps to NM_001159726.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:88775898 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:88854585 C>A maps to NM_016083.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:133769306 T>A maps to ENST00000452339 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:154727694 G>A maps to NM_173515.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:157222595 G>T maps to ENST00000367148 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr6:159404768 C>T maps to NM_031924.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:21826249 C>T maps to NM_003777.3 L3209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:24756951 G>A maps to NM_001127453.1 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:28763906 T>A maps to NM_182898.2 C220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:30831103 C>G maps to NM_032222.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:31014104 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:39247148 C>A maps to NM_007252.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:48081009 C>T maps to ENST00000430738 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:48316090 A>G maps to NM_152701.3 L2276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:50468168 G>T maps to NM_006060.3 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:53103681 C>G maps to NM_182595.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:75890732 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:76950708 A>G maps to NM_017439.3 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:91503774 A>T maps to NM_006980.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:98256631 C>T maps to NM_002523.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:99097526 G>A maps to NM_032164.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:100280766 G>C maps to NM_022574.4 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr7:154598702 G>T did not map to a codon.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:48694763 A>G maps to NM_006904.6 L3815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:70744122 G>T maps to NM_030958.2 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:110410760 C>G maps to ENST00000426474 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:113299302 T>C maps to NM_198123.1 P3107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:140715045 G>A maps to NM_016601.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr8:142441036 G>T maps to NM_032611.1 G139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:32544066 C>T maps to NM_005802.4 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:35792644 A>G maps to NM_003995.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:37745550 A>T maps to NM_014907.2 P1174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:72333392 C>A maps to NM_001099666.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:80043924 C>T maps to NM_004297.3 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:86518141 G>A maps to NM_017576.1 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:90266557 C>T maps to NM_004938.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:100433474 G>A maps to NM_002486.4 Q789Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:115931550 T>A maps to ENST00000446284 T1171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:127623765 C>T maps to NM_007209.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:135458597 A>G maps to NM_020064.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chr9:137687130 C>G maps to NM_000093.3 P923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chrX:1719724 G>T maps to NM_005088.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chrX:55777614 G>T maps to NM_016656.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chrX:67431997 T>C maps to NM_002547.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chrX:101153124 A>T maps to NM_001011657.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QI-01A-11D-A21Z-08 chrX:152807361 G>A maps to NM_001001344.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:15789242 C>T maps to ENST00000375924 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:32204222 C>T maps to NM_001703.2 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:46976773 C>A maps to NM_147192.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr1:89323051 G>A maps to NM_001514.5 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:7774362 G>A maps to NM_002216.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:27688158 G>A maps to NM_001034842.3 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:75011599 G>A maps to NM_016065.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:90427423 G>A maps to NM_001198829.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr10:124348478 C>T maps to ENST00000368915 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:1267502 G>A maps to ENST00000447027 T3134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:27398721 G>T maps to NM_018490.2 C364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:76944072 G>A maps to ENST00000376217 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:76944075 G>A maps to ENST00000376217 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr11:102586119 A>G maps to NM_002424.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr12:113325676 G>A maps to NM_001143854.1 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr12:113742152 C>T maps to NM_024959.2 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr13:35731302 G>T maps to ENST00000400445 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr13:73649891 C>T maps to NM_001730.3 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:21359943 G>T maps to NM_002935.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:95884263 G>A maps to NM_152592.3 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr14:100118592 C>T maps to NM_001127258.1 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr15:63128202 C>G maps to NM_015059.2 S2435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr16:46766180 C>A maps to NM_182493.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr16:67695398 G>A maps to NM_016948.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr17:61910949 G>A maps to NM_001098426.1 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:619038 G>A maps to NM_005035.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:12491948 T>C did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:12491954 A>C did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:18234407 G>A maps to NM_015016.1 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr19:34895678 C>T maps to NM_032346.1 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:39505627 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:73717137 A>G maps to NM_015120.4 V2683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:121708926 C>G maps to NM_005270.4 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:240061421 C>T maps to NM_006037.3 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr2:242065893 C>T maps to ENST00000358649 R812R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr20:472990 C>T maps to NM_177559.2 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr20:33162907 C>T maps to NM_080476.4 Q398Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr20:36760816 G>A maps to NM_004613.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr21:31859545 G>T maps to NM_181608.1 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr21:35468621 G>C maps to NM_006933.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr3:3887650 G>A maps to NM_020873.5 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr3:11340867 T>C maps to NM_006395.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr4:1107303 A>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr4:15542458 G>A did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr4:41263745 C>T maps to NM_004181.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:7695948 C>G maps to NM_020546.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:17275798 C>T maps to NM_006317.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:123983601 T>C maps to NM_020747.2 K825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr5:140188664 C>T maps to NM_018907.2 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr6:1612317 C>T maps to NM_001453.2 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr7:154564586 C>T maps to NM_130797.2 H357H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr8:53568650 T>C maps to NM_014781.4 L1246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr8:70588852 G>A maps to NM_030958.2 R694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr8:139609213 C>T did not map to a codon.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr9:115171289 C>T maps to NM_032303.4 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chr9:115806345 C>T maps to NM_003408.1 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chrX:99888428 C>T maps to NM_003270.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chrX:119589269 G>A maps to NM_013995.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chrX:140995383 C>T maps to NM_005462.4 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A3QK-01B-11D-A23M-08 chrX:152915678 G>T maps to NM_001395.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:28362170 G>C maps to NM_001990.2 S82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:28817514 C>G maps to NM_023923.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:155112685 G>A maps to NM_018973.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr1:190068167 C>T maps to NM_199051.1 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr10:89717614 C>T maps to NM_000314.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr10:112838905 G>A maps to NM_000681.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:30439146 T>C maps to NM_001584.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:55595182 T>C maps to NM_001004739.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:62415418 C>T maps to NM_030628.1 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:64939958 T>C maps to NM_001008778.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr11:65315516 C>T did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr12:21427509 A>C maps to NM_134431.3 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr12:50044478 C>T maps to NM_175736.4 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:23344897 G>A maps to NM_014045.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:24878128 C>T maps to NM_025081.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:45658162 A>C maps to NM_020937.2 A1646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:60193838 G>T maps to NM_021136.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr14:105408167 G>A maps to NM_138420.2 A4540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:29346683 G>A maps to NM_005503.3 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:42054513 G>A maps to ENST00000219905 R2615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:64968121 G>A maps to NM_015042.1 K1023K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:76995193 G>A maps to ENST00000324767 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:78790482 T>C maps to NM_004136.2 *964Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr15:88670428 G>A maps to NM_001012338.1 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr16:427569 G>A maps to NM_021259.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr17:3438936 G>A maps to ENST00000381913 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr18:31326429 A>T maps to NM_030632.1 A2206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:1080304 G>A maps to NM_012292.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:1817223 G>A maps to NM_020695.3 C1065C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:2733468 C>G maps to NM_144564.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:11313295 C>T maps to ENST00000319867 S1777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:21991452 G>C maps to NM_003423.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:39516074 C>T maps to NM_178820.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:46278205 C>G did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:52570183 G>C maps to NM_001136499.1 Y317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr19:56539146 C>T maps to NM_153447.4 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:18757542 G>A maps to ENST00000455492 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:73493770 C>T maps to ENST00000295133 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:170063206 G>C maps to NM_004525.2 V2341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr2:179474919 G>T maps to NM_133378.4 L14543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr20:33762598 G>A maps to NM_006404.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr20:37153560 C>A maps to NM_020336.2 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr21:44174149 C>T maps to NM_002606.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr22:35808506 C>T maps to NM_006739.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr22:40814491 G>A maps to NM_020831.3 I650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr3:38783970 A>C maps to NM_006514.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr3:52962227 G>A maps to NM_016329.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:41941218 T>C maps to NM_018126.2 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:123900542 T>G did not map to a codon.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr4:170017809 G>A maps to NM_020870.3 Q843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:5457793 G>C maps to NM_015325.1 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:140568499 G>A maps to NM_019119.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:140890658 C>T maps to NM_018915.2 N906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr5:145890060 A>G maps to NM_006706.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr6:31918656 C>G maps to ENST00000437789 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr6:136600966 G>T maps to NM_014739.2 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr6:148864864 C>G maps to NM_015278.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:2956959 G>C maps to NM_032415.4 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:82585933 C>T maps to NM_033026.5 Q1445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:143701409 C>G maps to NM_001005281.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr7:150845867 G>A maps to NM_001098834.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr8:98288923 C>T maps to NM_033512.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr9:34977115 G>T maps to NM_015297.1 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chr9:131010867 G>T maps to ENST00000372923 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40E-01A-12D-A23M-08 chrX:23411318 G>T maps to NM_173495.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:37319236 C>A maps to NM_000831.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:70616830 C>T maps to NM_017768.4 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:158325144 C>T maps to NM_030893.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:190067738 A>C maps to NM_199051.1 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:208072506 A>G maps to NM_001025109.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:223177435 G>A maps to NM_032890.2 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr1:223465952 G>A maps to NM_017982.3 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:1605846 G>A maps to NM_001005922.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:4967469 C>T maps to NM_001005329.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:58126260 G>A maps to NM_001005489.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr11:111853165 A>G maps to NM_001037954.2 *291W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:23793805 G>T maps to NM_006940.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:32136194 C>A maps to NM_018169.3 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:50044616 C>T maps to NM_175736.4 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr12:95656755 G>T maps to NM_017599.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr13:49050980 T>C did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr15:28456241 G>A maps to NM_004667.4 I2325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr16:71682798 T>A maps to NM_015020.2 A1322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:3119783 G>A maps to NM_014565.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:27011885 G>T maps to NM_003170.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:34894045 C>T maps to NM_178517.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:48628893 T>C maps to NM_022827.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:74011019 G>A maps to NM_001988.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:78180860 C>T maps to NM_024110.2 N928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr17:80400083 G>A maps to NM_173620.2 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:17295780 C>T maps to NM_004145.3 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:18779241 G>A maps to NM_018316.1 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:35449113 G>A maps to NM_175872.4 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:44832185 G>A maps to ENST00000412927 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:47646783 G>A maps to NM_005500.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:48919344 C>T maps to NM_000836.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr19:54314477 C>A maps to ENST00000391773 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:74756362 G>A maps to ENST00000258081 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:165350940 T>C maps to NM_004490.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:167108338 T>C maps to ENST00000303354 G1137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:179634498 G>A maps to NM_133378.4 Q2937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:206872143 C>T maps to NM_017759.4 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr2:234878871 G>A maps to NM_024080.4 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:43138621 G>A maps to NM_006811.2 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:44756828 C>A maps to NM_001250.4 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr20:61943385 C>T maps to ENST00000326996 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr22:30659955 G>A maps to NM_020530.3 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr22:32330183 G>A maps to NM_015372.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr3:6903548 G>A maps to NM_181874.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr3:44636002 T>G maps to NM_173658.1 Y106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr4:42895367 C>T maps to NM_001080476.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr4:85634392 C>T did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr4:186112119 T>C maps to NM_020827.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr5:172517871 A>G maps to NM_153607.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr6:34574586 C>G maps to NM_024294.2 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr6:129649558 T>C did not map to a codon.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr6:152651704 G>A maps to NM_182961.2 A4705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:27285923 G>A maps to NM_001989.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:93055889 G>A maps to NM_001164737.1 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:95442531 G>A maps to NM_004411.4 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr7:100731303 G>A maps to NM_030961.1 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr8:52321798 G>A maps to NM_144651.4 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr9:130265126 G>A maps to NM_001005374.2 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr9:136409599 C>T maps to ENST00000393061 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chr9:139750012 G>A maps to ENST00000392881 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chrX:69626161 C>T maps to NM_012310.4 T1010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GV-A40G-01A-11D-A23M-08 chrX:107433640 T>A maps to NM_033641.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr1:36636770 G>A maps to NM_018067.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr1:205273536 G>A maps to ENST00000441520 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr1:228433249 G>A maps to NM_001098623.1 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:102296388 G>A maps to ENST00000442724 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:124740003 C>T maps to NM_153336.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr10:126523362 C>T maps to NM_032182.3 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr11:35640996 C>T maps to NM_014344.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr11:56185063 G>T maps to NM_001004744.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr12:93149619 G>A maps to NM_001004330.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr14:64921556 C>T maps to NM_005956.3 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr16:88098938 G>T did not map to a codon.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr17:16029477 C>A maps to ENST00000395857 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr17:26821082 C>T maps to NM_001145975.1 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:10116236 G>A maps to NM_015719.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:37903794 G>A maps to NM_152484.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:38682829 G>A maps to NM_015073.1 L1492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr19:41188698 T>C maps to NM_004756.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:20202934 C>T maps to NM_002381.4 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:27361073 G>A maps to NM_178553.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:54531937 A>G maps to NM_138448.3 *100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:88894995 A>G maps to NM_004836.5 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr2:209189657 A>T maps to NM_015040.3 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr20:35064674 C>A maps to ENST00000339266 S388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr20:57875893 C>T maps to NM_207034.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr22:41833079 C>T maps to NM_016272.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr3:112998755 G>A maps to ENST00000273395 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr3:113753923 C>T maps to NM_020817.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr4:88099701 G>A maps to NM_020803.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr4:155506819 C>G maps to NM_000508.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr5:140215821 G>C maps to NM_018910.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:29694775 C>A maps to NM_001098479.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:31785218 C>T maps to NM_005345.5 I562I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:93955098 T>C maps to NM_004440.3 Q933Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr6:105225169 C>T maps to NM_020771.3 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr7:28843820 G>A maps to NM_182898.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr7:95157437 C>T maps to NM_016116.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chr9:95219644 G>T maps to NM_017680.4 Y356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chrX:53283762 A>G maps to NM_001111125.1 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HO-01A-11D-A17V-08 chrX:118109239 C>G maps to NM_001031855.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:11007720 C>T maps to NM_001170754.1 *824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:12429572 G>T maps to NM_015378.2 E3542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:15813790 T>A maps to ENST00000442979 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:16459809 C>A maps to NM_004431.3 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:19441310 C>T maps to ENST00000375267 R3732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:24021181 C>T maps to NM_000975.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:35579263 C>T maps to NM_024772.3 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:36298148 C>T maps to NM_017629.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:82421723 C>G maps to ENST00000370717 S662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:107867235 G>A maps to NM_001113226.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:110882178 C>A maps to NM_022768.4 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:117297378 C>G maps to NM_001767.3 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:150551724 C>G maps to NM_021960.4 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:161276625 C>T maps to ENST00000360451 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:172526518 T>A maps to ENST00000367723 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:176913087 G>T maps to ENST00000281881 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:179310345 C>T maps to NM_003101.4 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:207135776 G>A maps to NM_001170631.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:208072531 G>C maps to NM_001025109.1 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:216052272 T>A maps to ENST00000366943 S2797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:232596868 C>T maps to NM_020808.3 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:234452364 C>T maps to NM_173508.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:247323034 G>C maps to NM_003431.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr1:248129259 G>A maps to NM_001004491.1 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr10:72520584 C>T maps to NM_139155.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr10:99160976 C>T maps to NM_015179.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:319921 C>T maps to NM_021034.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:7984931 C>T maps to NM_176821.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:8132429 C>A maps to ENST00000309737 E309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:20178726 C>T maps to ENST00000227256 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:47819814 C>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:57569393 C>G maps to NM_001085458.1 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:60703932 C>T maps to NM_017870.3 Q877*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:65088416 C>T maps to NM_006779.2 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:66619931 G>C maps to NM_022172.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:67223785 C>T maps to NM_145200.3 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:104877903 C>T maps to NM_001136112.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:110128892 T>G maps to ENST00000405097 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:118881533 C>T maps to NM_198489.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr11:124294479 A>G maps to NM_001005196.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:4599750 G>A maps to NM_020374.2 F501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:6143928 G>A maps to NM_000552.3 I870I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:6664601 C>T maps to NM_001193457.1 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:13240940 G>A maps to NM_001080555.1 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:15073906 C>A maps to NM_152321.2 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:27148172 G>A maps to NM_016551.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:32136972 C>T maps to NM_018169.3 S1028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:49446361 C>A maps to NM_003482.3 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:49446374 C>G maps to NM_003482.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:105388289 C>G maps to NM_152318.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:113314468 G>A maps to NM_001143854.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr12:123494487 G>A maps to NM_020845.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:35926316 T>C maps to ENST00000400445 A2012A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:46287726 C>G maps to NM_152719.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:73334744 A>G maps to NM_014953.3 D905D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:75900526 T>A maps to ENST00000431480 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr13:113208460 G>C maps to NM_006322.4 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:24687355 G>A maps to NM_006156.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:25045380 C>A maps to NM_001911.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:45679580 A>C did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:52781367 C>T maps to NM_000956.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr14:64497984 C>G maps to NM_182914.2 G2377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr15:54008833 A>T maps to NM_182758.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr15:62219319 G>C maps to NM_020821.2 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:2110795 G>A maps to NM_000548.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:2868795 C>T maps to NM_006799.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:3641147 C>A maps to NM_032444.2 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:4431069 C>T maps to NM_138440.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:11444613 G>A maps to NM_152308.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:27221611 C>T maps to NM_001145348.1 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:30780184 G>A maps to NM_014771.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:67768936 G>C maps to NM_020850.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:71482034 G>C maps to NM_145911.1 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr16:89813042 G>A maps to NM_000135.2 F1154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:4841335 C>T maps to NM_003562.4 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:10216042 C>A maps to NM_003802.2 E1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:10243491 C>G maps to NM_003802.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:17924526 G>C maps to NM_145691.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:18042858 C>T maps to ENST00000205890 F1715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:19608793 G>C maps to NM_152908.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:19646658 G>A maps to NM_000691.4 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:27999020 G>A maps to NM_033389.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:30814981 C>A maps to NM_003885.2 S115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:38151528 G>A maps to NM_002809.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:39019990 C>T maps to NM_000223.3 Q311Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr17:42290268 G>T maps to NM_014233.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr18:47369613 C>T maps to NM_001080467.2 L1536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr18:72343703 C>G maps to NM_017757.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:1271018 C>T maps to ENST00000413636 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:2339821 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:8670586 G>T maps to NM_030957.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:14231398 C>A maps to NM_018154.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:17737461 G>A maps to ENST00000428389 I1439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:33444535 C>T maps to NM_032816.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:39759823 C>A maps to NM_172138.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:52507118 T>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:55918273 C>A maps to NM_014501.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:56156282 G>T maps to NM_016535.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:56175099 C>G maps to NM_007279.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr19:57058945 C>T maps to NM_020828.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:24261332 C>G maps to NM_025203.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:26706368 G>C maps to NM_194248.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:37505008 C>G maps to NM_005813.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:86280075 C>T maps to NM_015425.3 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:100020218 C>T maps to NM_016316.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:109087477 C>T maps to NM_181453.3 Q565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:128913069 C>T maps to NM_020120.3 F715F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:168105338 G>A maps to NM_152381.5 Q2479Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:179399172 C>A maps to NM_133378.4 E31489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:179578816 G>C maps to NM_133378.4 T7612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr2:228881822 C>T maps to NM_001142644.1 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:3783804 G>A maps to NM_021873.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:33596492 C>T maps to NM_015638.2 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:34219935 T>A maps to NM_003915.5 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:34596336 C>T maps to ENST00000373973 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:36625250 G>A maps to NM_014657.1 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:39316773 C>T maps to NM_005461.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:42086759 C>G maps to NM_006275.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:42635185 G>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:43804727 G>A maps to NM_002638.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:46279913 C>T maps to NM_181659.2 F1280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:56136481 G>A maps to NM_002591.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:62571632 G>A maps to NM_017859.3 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr20:62624834 C>G maps to NM_012469.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr21:31798110 G>A maps to NM_181622.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr21:40800152 C>T maps to NM_152505.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr21:46058038 C>T maps to NM_181688.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:19384470 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:31731849 C>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:41625592 G>A maps to NM_031488.4 K646K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:44514967 G>A maps to NM_001003828.1 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr22:50969698 C>G maps to NM_001014440.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:424355 T>A did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:27446454 C>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:44763892 C>T maps to NM_033210.4 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:47887267 G>T maps to NM_138615.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:49363262 G>A maps to NM_003363.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:51112864 T>C maps to NM_004947.4 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:126272146 G>A maps to NM_152533.1 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:130828670 C>T maps to NM_024800.4 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr3:182681825 C>A maps to NM_020640.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:628476 C>T maps to NM_000283.3 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:48106973 T>C did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:85634325 C>A maps to NM_014991.4 T2676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:96761706 C>T maps to NM_005390.4 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:123117943 A>C maps to NM_015312.3 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:157684304 G>C maps to NM_016205.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:167020651 G>T maps to ENST00000507499 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:169931102 G>A maps to NM_032783.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr4:177608516 G>C maps to NM_005429.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:1087071 C>T maps to NM_006598.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:23526573 G>A maps to NM_020227.2 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:32239279 C>G did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:40692209 C>G maps to NM_000958.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140052880 C>T maps to NM_194249.2 Q39Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140176231 C>T maps to NM_018905.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140348185 C>A maps to NM_018899.5 S612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:140793479 C>T maps to NM_018913.2 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:147015814 G>A maps to NM_014790.3 F549F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr5:176304244 G>A maps to NM_133369.2 E477E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:592508 G>C maps to NM_018303.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:26188993 C>T maps to NM_003539.3 *104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:26413832 C>T maps to NM_007048.5 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:33165551 G>A maps to ENST00000374685 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:37451063 C>T maps to NM_138493.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:41002619 G>C maps to NM_173561.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:72678706 G>A maps to NM_014989.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:87994087 G>A maps to NM_198568.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr6:147648323 C>G maps to NM_001127715.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:6227346 C>T maps to ENST00000396741 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:6227352 C>T did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:28858827 G>T maps to NM_182898.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:66409967 G>A maps to NM_017994.4 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:99319921 C>T maps to ENST00000292414 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:99821276 T>A maps to NM_178831.6 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:100479835 C>T maps to NM_015908.5 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:100730634 G>A maps to NM_030961.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr7:128355535 C>G maps to NM_032599.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:24324309 A>C did not map to a codon.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:48803018 A>C maps to NM_006904.6 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:70585511 G>A maps to NM_030958.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:88885179 G>A maps to NM_152418.3 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:95508023 G>A maps to NM_015496.3 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:124253562 G>A maps to NM_032847.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:133645150 G>T maps to ENST00000250173 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:144378378 G>A maps to NM_030895.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr8:144662723 C>T maps to NM_032378.4 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr9:37735727 C>T maps to NM_014907.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr9:90535925 A>C maps to NM_001145124.1 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chr9:116930563 G>A maps to NM_032888.2 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chrX:9864155 C>G maps to NM_001649.2 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chrX:65824269 C>T maps to ENST00000450752 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chrX:77224637 G>A maps to NM_001029891.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H4-A2HQ-01A-11D-A17V-08 chrX:105882903 C>A maps to NM_018015.5 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:109806338 C>T maps to NM_001408.2 R1647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:151260359 C>T maps to NM_020832.1 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:159557900 G>C maps to NM_001639.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr1:161480705 T>A maps to NM_001136219.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr10:68979429 G>A maps to NM_013266.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:36614206 G>T maps to NM_000536.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:55587182 C>G maps to ENST00000395203 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:74556165 C>A maps to NM_182969.1 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr11:122795697 C>T maps to NM_024806.2 Q320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:6958993 C>T maps to NM_031299.4 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:7177162 T>A maps to NM_001734.3 C425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:32955490 C>A did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:50571471 G>C maps to NM_001113546.1 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:56865967 G>C maps to NM_013267.2 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:69127365 G>T maps to NM_020401.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:120565653 C>T maps to NM_006836.1 *2672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr12:125473493 G>A maps to NM_032656.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:23890798 G>C maps to NM_019066.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:42439885 C>A maps to ENST00000397272 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:55919292 G>C maps to NM_173814.4 S947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:65447317 G>A maps to NM_006660.3 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr15:79749967 T>C maps to NM_015206.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr16:3339612 G>A maps to NM_005741.4 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr16:89724677 C>T maps to NM_153025.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr17:11648244 G>A maps to NM_001372.3 K2081K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr17:26945871 C>G maps to NM_014680.2 L1920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr17:70119894 G>A maps to NM_000346.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:10477208 C>T maps to NM_003331.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:10624778 G>A maps to NM_001166215.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:11031349 C>T maps to NM_199141.1 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:11526624 G>A maps to NM_001161616.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:18896512 C>T maps to NM_000095.2 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr19:40909733 C>T maps to NM_181882.2 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:179457373 C>T maps to NM_133378.4 L17218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:185803314 G>A maps to NM_194250.1 K1064K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr2:242046891 C>T maps to ENST00000358649 G1237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr20:30674543 C>T maps to NM_002110.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr20:43929793 C>A maps to ENST00000372754 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr20:61458603 C>T maps to NM_001853.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr22:30858093 C>T maps to NM_174975.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr3:17052784 T>C maps to NM_001144382.1 N645N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr3:123383092 C>A maps to NM_053025.3 E1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr4:84193255 C>T maps to NM_015697.7 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr4:88414988 G>A maps to NM_004684.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr5:33937234 G>A maps to NM_016568.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr5:134086447 G>C did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr5:170883751 C>T maps to NM_003862.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr6:31322893 C>T maps to ENST00000428231 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr6:42893344 C>G maps to NM_138296.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr7:91981820 G>A maps to NM_019004.1 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr7:152373251 C>G did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr8:6912953 C>T maps to NM_021010.1 *95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr8:76468214 A>T did not map to a codon.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr8:82592976 C>A maps to NM_001144878.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chr9:127781101 G>A maps to NM_173690.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chrX:1471229 C>G maps to NM_002183.2 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chrX:32503147 C>T maps to ENST00000357033 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chrX:101970045 T>G maps to NM_138437.5 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HQ-A2OE-01A-11D-A202-08 chrX:135441567 A>G maps to NM_153834.3 Q2366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:1262842 G>A maps to NM_001029885.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:19584360 C>T maps to NM_016183.3 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:24483774 G>A maps to NM_170743.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:28176863 C>G maps to NM_014110.4 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:32051352 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:36301504 G>A maps to NM_017629.2 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:39876003 G>T maps to NM_015038.1 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:108679439 T>C maps to NM_013386.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:158059371 G>T maps to ENST00000368173 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:159166680 C>G maps to NM_021189.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:161928234 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:171073095 G>A maps to NM_006894.5 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:177133536 G>A maps to ENST00000281881 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:203188876 G>T maps to NM_003465.2 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:205027350 C>T maps to NM_005076.3 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:223994609 G>A maps to NM_001031685.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:233120094 G>T maps to NM_014801.3 G2123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr1:241665790 G>T maps to NM_000143.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr10:50854653 C>G maps to NM_020549.4 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:1151640 G>C maps to ENST00000406844 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:61543556 C>T maps to NM_001127392.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:95712800 C>A maps to NM_032427.1 G928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:119142468 C>T maps to NM_005188.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr11:119216323 A>C maps to NM_031433.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:4735735 G>A maps to NM_006422.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:46245433 T>C maps to NM_152641.2 V1176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:53673529 G>A maps to NM_012291.4 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:79986469 G>A maps to NM_002583.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr12:81648680 G>T maps to NM_024560.2 E681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr13:23904688 G>T maps to NM_014363.4 G4442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr13:32945212 C>T maps to NM_000059.3 Q2870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr14:24769357 C>T maps to NM_174913.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr14:92537343 G>T maps to ENST00000359819 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr14:93709010 C>A maps to NM_001002860.2 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:41687142 C>A maps to NM_016013.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:48626676 G>A maps to NM_001025248.1 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:49800543 A>C maps to NM_152647.2 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:80467380 G>T maps to NM_000137.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:86273897 T>A maps to NM_006738.4 A2418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr15:89391183 G>A maps to NM_013227.3 K549K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr16:786282 G>C maps to NM_022493.1 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr16:67514920 C>T maps to NM_004691.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr16:67578264 C>T maps to NM_001193523.1 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:4080557 G>A maps to NM_016376.3 Q881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:41063349 C>T maps to NM_000151.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:43923858 G>A maps to NM_175882.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:73498742 A>T maps to NM_020753.3 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr17:74005730 C>T maps to NM_001988.2 K1185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:3548010 C>A maps to NM_021731.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:12595588 G>T did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:16601208 C>T maps to NM_145046.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:19339265 C>G maps to NM_004386.2 S946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:34818974 C>G maps to NM_014686.3 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:39976915 G>A maps to NM_001001563.1 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr19:50947073 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:26702465 C>T maps to NM_194248.2 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:27351314 C>A maps to NM_032604.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:44051154 G>C maps to NM_022436.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:56603021 A>G maps to NM_001080433.1 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:71058237 T>C maps to NM_015717.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:179323265 G>A maps to NM_001042702.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr2:239234476 C>T maps to NM_015650.3 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:9496202 G>C maps to NM_012261.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:30419637 C>T maps to NM_033118.3 N519N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:30419887 C>T maps to NM_033118.3 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:35064618 C>T maps to ENST00000339266 Y369Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr20:36641206 C>A maps to NM_014657.1 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr21:38098554 C>T maps to NM_005069.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr22:29966392 C>A did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:45812891 G>C maps to NM_020208.3 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:47604193 C>A maps to ENST00000383738 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:50197150 C>T maps to NM_004186.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:52400858 G>T maps to ENST00000273600 T1907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr3:186335075 C>T maps to ENST00000273784 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr4:187524559 G>T maps to ENST00000260147 S3710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr5:78359610 C>G did not map to a codon.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr5:82835421 T>A maps to NM_004385.4 T2200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr5:180661585 G>A maps to NM_033549.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:33288741 G>A maps to NM_001350.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:36168215 G>A maps to NM_015695.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:42974674 C>T maps to NM_006245.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:49666125 G>A maps to ENST00000211238 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr6:160205737 G>A maps to NM_030752.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr7:48312667 C>A maps to NM_152701.3 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr7:100675896 C>G maps to NM_001040105.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:18393455 C>A maps to ENST00000440756 E983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:41572562 G>T maps to ENST00000415018 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:120790294 T>C maps to NM_003184.3 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:134475668 C>T maps to NM_173344.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr8:145624758 C>T maps to NM_013291.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:34662357 G>C maps to NM_006664.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:35396569 C>T maps to ENST00000396787 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:100245528 G>A maps to NM_014290.2 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chr9:131475650 C>T maps to NM_013355.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chrX:69255457 A>G maps to NM_001399.4 *392W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chrX:117892056 C>T maps to NM_001560.2 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chrX:128614760 G>A maps to NM_003069.3 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chrX:153539539 C>T maps to NM_012253.3 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WS-01A-11D-A22Z-08 chrX:153539540 A>T maps to NM_012253.3 K208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:1572052 C>T maps to ENST00000401097 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:31439029 G>A maps to ENST00000373741 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:46650907 T>C maps to NM_005727.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:152325729 G>C maps to NM_001014342.2 S1511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:161641371 C>T maps to NM_004001.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:200946380 G>A maps to NM_017596.2 Y1415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:213415602 C>T maps to NM_012424.3 R928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr1:235826287 C>T maps to NM_000081.2 L3786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr10:82269070 C>A maps to NM_030927.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr11:8724141 G>C maps to NM_005418.3 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr11:71276977 C>T maps to ENST00000422553 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr11:92703068 C>T maps to NM_005959.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:48360996 C>T maps to NM_001143842.1 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:64485154 C>G maps to NM_020762.2 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr12:71016175 A>G maps to NM_001109754.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr13:97986693 G>T maps to ENST00000376673 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr14:37145474 C>T maps to NM_006194.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr14:88934486 G>C maps to NM_007039.3 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:30021405 G>A maps to NM_003586.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:50339458 C>T maps to NM_001114.3 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:67213338 C>A maps to NM_001040715.1 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:68009820 G>A maps to NM_022357.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr16:70513197 C>T maps to NM_145059.2 H1015H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr17:649461 G>C maps to NM_015721.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr18:21427491 G>A maps to ENST00000416669 T1334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr18:77659422 C>T maps to NM_012283.1 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:18120727 C>T maps to NM_015683.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:36278973 C>T maps to ENST00000007510 Y1169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:42910493 C>T maps to NM_005357.2 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:47773834 G>A maps to NM_015603.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:51628542 G>A maps to NM_014441.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr19:57335704 G>T maps to NM_006210.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:12863642 C>T maps to NM_021643.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:27665506 C>T maps to NM_001168364.1 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:111408234 A>G maps to NM_004336.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:125671723 G>C maps to NM_130773.2 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr2:242169087 G>A maps to NM_005336.3 S1245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr20:3146670 A>C maps to NM_014731.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr20:56098313 C>T maps to ENST00000423479 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:12447543 G>C maps to NM_015869.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:12861591 A>G maps to NM_001162499.1 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:37476521 C>T maps to NM_178339.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:46414767 T>C maps to NM_001100168.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:49211747 T>C maps to NM_173546.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:112358446 C>T maps to ENST00000447230 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr3:169540296 C>T maps to NM_001080460.1 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:39448823 C>T maps to NM_175737.3 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:52861828 C>T maps to NM_001024611.1 E453E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:95170810 G>T maps to NM_001128429.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:126240574 C>T maps to NM_024582.4 V1003V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr4:153244184 G>A maps to NM_033632.2 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:75902128 G>A did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:140230131 G>T maps to NM_031857.1 V684V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:141050833 G>C maps to NM_022481.5 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr5:145512561 G>T maps to NM_020117.9 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:1313430 C>A maps to NM_033260.3 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:8041459 C>T maps to NM_201280.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:31079946 G>A maps to NM_014070.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:33243656 T>C maps to NM_022551.2 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:35088698 G>C maps to NM_001093728.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:35387982 C>G maps to NM_006238.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:50696936 G>C maps to NM_172238.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:119300684 T>C did not map to a codon.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr6:159046149 C>T maps to NM_020823.1 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:41790658 T>G maps to NM_006766.3 P1693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:57079983 C>T maps to NM_002655.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:68334768 G>T maps to NM_020361.4 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr8:142161800 C>T maps to NM_014957.2 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:19119734 A>T maps to NM_001122.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:19119763 C>A maps to NM_001122.2 G221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:34372104 C>T maps to NM_020702.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:34372875 T>C maps to NM_020702.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:136324256 G>A maps to NM_139025.3 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chr9:137328330 C>G maps to NM_002957.4 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chrX:47092453 C>T maps to NM_004651.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WU-01B-11D-A23M-08 chrX:153420213 G>A maps to NM_020061.4 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr1:27106538 G>A maps to NM_006015.4 W2050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr10:94821037 G>A maps to NM_183374.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr10:101571350 A>T maps to NM_000392.3 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr11:22249086 C>T maps to NM_213599.2 I201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr11:65649733 G>A maps to NM_001335.3 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr11:116701558 C>T maps to ENST00000360377 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr12:39760202 A>G maps to ENST00000395670 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr14:70515700 G>A maps to NM_183002.1 Y730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr14:95579562 T>A did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:11325226 A>G did not map to a codon.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:46341739 C>T maps to NM_004819.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:47197162 G>A maps to ENST00000449438 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr19:51535177 G>T maps to NM_019598.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:70515287 A>T maps to NM_003096.2 L31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:97370380 A>G maps to NM_001113382.1 T2078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:105473458 G>C maps to NM_006236.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:141079601 A>T maps to NM_018557.2 S4190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr2:228104884 C>T maps to NM_000091.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr20:5904367 C>T maps to NM_001819.2 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr22:45719181 C>T maps to NM_017911.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr4:961426 C>T maps to NM_001347.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr4:71522980 G>T maps to NM_144646.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr7:39472815 G>T maps to NM_007252.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr8:10555319 C>T maps to NM_001040032.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K4-A3WV-01A-11D-A22Z-08 chrX:50659528 C>T maps to NM_005448.2 V367V. Only missense variants will be evaluated by CHASM.
