5064 NP_705833 S270L not found in SNVbox database
8379 NP_001070868 M1I not found in SNVbox database
510 NP_001070868 V38I not found in SNVbox database
1417 NP_001070868 R201H not found in SNVbox database
1592 NP_705833 R420K not found in SNVbox database
2053 NP_001070868 F303L not found in SNVbox database
3187 NP_705833 V434I not found in SNVbox database
4556 NP_705833 V525M not found in SNVbox database
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr19:58863781 C>T maps to NM_130786.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr10:52595832 C>A did not map to a codon.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr10:52619637 G>A maps to NM_138932.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:7657341 T>G did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:7645570 C>T maps to NM_145891.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr16:7703829 G>A maps to NM_145891.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr12:9230010 T>G maps to NM_000014.4 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DQ-01A-11D-A377-08 chr12:9248203 G>T maps to NM_000014.4 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:9229986 G>A maps to NM_000014.4 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:9246170 T>C maps to NM_000014.4 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:43089594 G>A maps to NM_017436.4 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:151545614 C>T maps to NM_001086.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr1:12726652 C>T maps to NM_001013630.1 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr1:12721808 C>G maps to NM_001013630.1 Y131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:69757828 C>T maps to NM_014911.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:44268379 C>T maps to NM_020745.2 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr7:121726064 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:121773657 C>T maps to NM_005763.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:35345869 C>T maps to NM_012138.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr9:107645338 C>T maps to NM_005502.3 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:107602599 G>A maps to NM_005502.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:107589249 G>A maps to NM_005502.3 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr9:107576491 G>A maps to NM_005502.3 R1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:215890473 G>A maps to NM_173076.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:48327659 G>A maps to NM_152701.3 A2980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr7:48315046 C>T maps to NM_152701.3 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:48318293 T>C maps to NM_152701.3 T2501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr7:48443342 C>A maps to NM_152701.3 G3979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr7:48352728 C>T maps to NM_152701.3 S3194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr7:48428692 C>T maps to NM_152701.3 L3844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr7:48428730 T>A maps to NM_152701.3 A3856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr7:48318264 C>T maps to NM_152701.3 L2492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr7:48314143 T>C maps to NM_152701.3 A1627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:48619870 C>A maps to NM_152701.3 Y4802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr7:48280529 G>T maps to NM_152701.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr9:139912648 G>A maps to ENST00000355090 Y688Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139904443 G>A maps to ENST00000355090 D2192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139904575 G>A maps to ENST00000355090 S2148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139907309 C>T maps to ENST00000355090 A1675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139912117 G>A maps to ENST00000355090 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:2336813 G>A maps to NM_001089.2 A1053A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr16:2334346 G>A maps to NM_001089.2 Y1265Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2329103 G>A maps to NM_001089.2 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr1:94506836 G>A maps to NM_000350.2 C1150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:94497573 G>A maps to NM_000350.2 N1296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr1:94517207 C>T maps to NM_000350.2 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67252296 C>T did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:67300890 G>C maps to ENST00000392677 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OA-01A-11D-A41K-08 chr17:67246064 A>G maps to ENST00000392677 S1583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:1058147 C>T maps to NM_019112.3 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr19:1043360 C>T maps to NM_019112.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:1046291 C>T maps to NM_019112.3 F503F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr19:1050919 G>C maps to NM_019112.3 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:66873751 C>T maps to NM_007168.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr17:67040649 A>C maps to NM_080283.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:87133633 C>A maps to NM_000927.3 T1256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:229666036 C>T maps to NM_012089.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:229667479 T>C did not map to a codon.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr2:169826553 C>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr7:87082327 A>G maps to NM_018849.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:87104730 C>T maps to NM_018849.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr7:87037487 G>A maps to NM_018849.2 N1048N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:20685386 C>T maps to NM_001163941.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:20721256 C>T maps to NM_001163941.1 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr23:74318817 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:43403512 C>T maps to NM_033450.2 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:48239324 G>A maps to NM_032583.3 R602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:48247383 C>T maps to NM_032583.3 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:48121985 C>T maps to NM_033226.2 S1162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:48741194 G>T maps to NM_003786.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr17:48745030 C>A maps to NM_003786.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48738335 C>T maps to NM_003786.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48753278 C>T maps to NM_003786.3 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr13:95862990 G>C maps to NM_005845.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr13:95715068 G>A maps to NM_005845.3 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr13:95858796 G>A maps to NM_005845.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr3:183667863 G>A maps to NM_005688.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:183696308 G>A maps to NM_005688.2 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:183703151 G>A maps to NM_001023587.1 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr16:16256865 G>A maps to NM_001171.5 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr11:17415833 C>T maps to ENST00000302539 T1509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:17438496 G>A maps to ENST00000302539 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:17450216 G>A maps to ENST00000302539 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr12:22035726 G>A maps to NM_005691.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153001620 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr12:39994383 A>G maps to NM_005164.3 Y545Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr12:40010811 A>C maps to NM_005164.3 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:94980699 A>G did not map to a codon.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr1:94946039 C>A maps to ENST00000454898 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr21:43693445 C>T maps to NM_004915.3 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr11:119027720 T>C maps to NM_001142505.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:44040308 A>T maps to NM_022436.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:44100940 C>T maps to NM_022437.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27353416 C>T maps to NM_032604.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:73151924 T>C maps to NM_148912.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr20:25300845 G>A maps to NM_015600.3 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr13:108881586 G>A maps to NM_032859.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52011972 G>A maps to ENST00000463937 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:89698745 G>A maps to NM_152924.4 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr19:17405641 G>A maps to NM_024527.4 C258C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:116207735 C>T maps to ENST00000277895 K614K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:148586655 C>T maps to NM_014945.2 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr7:150554544 C>T maps to ENST00000416793 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:916347 G>A maps to NM_021962.2 N616N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:994937 G>A maps to NM_021962.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr3:127399140 G>A maps to NM_172027.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:38167087 C>T maps to NM_001607.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr17:35536314 A>T maps to NM_198834.1 T1655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:35563695 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:35591984 G>A maps to NM_198834.1 R1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:35632931 G>A maps to NM_198834.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:109693957 G>A maps to NM_001093.3 T2060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr12:109703024 T>C maps to NM_001093.3 S2351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr12:112153742 C>T maps to NM_001136538.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr12:121164961 G>A maps to NM_000017.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr17:7126072 G>A maps to ENST00000356839 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr17:7240073 C>T maps to NM_014716.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:32483082 G>A maps to NM_001094.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr17:31618455 G>A maps to NM_183377.1 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr12:50472232 C>A maps to NM_020039.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:220396490 C>T maps to NM_018674.4 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr11:44100334 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr11:44092837 A>G maps to NM_032592.3 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:44097101 G>A maps to NM_032592.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:44099414 C>T maps to NM_032592.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr11:44080232 C>T maps to NM_001031854.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr11:44069762 G>A maps to NM_001031854.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61556408 C>T maps to NM_000789.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61557710 G>T maps to NM_000789.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr23:15605909 G>C did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:100490934 G>A maps to NM_000665.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr7:100488844 G>A maps to NM_000665.3 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr7:100490250 G>A maps to NM_000665.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:23528662 C>T maps to NM_014977.3 E1240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:40034430 G>A maps to ENST00000401700 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:96810493 T>C maps to NM_020186.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:32440536 C>T maps to NM_002197.2 Y774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr22:41911451 C>T maps to ENST00000396512 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr2:111562875 G>A maps to NM_001142807.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:272205 C>T maps to NM_007099.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr3:141011305 C>T maps to NM_001037172.1 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr23:70828894 T>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:70823664 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:70817887 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:125547965 A>G maps to NM_001612.5 H93H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr15:78471896 C>G maps to NM_015162.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr15:78474319 G>A maps to NM_015162.4 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr15:78526788 G>A maps to NM_015162.4 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:89212410 C>T maps to NM_174917.2 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:185684392 C>T maps to NM_001995.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:185687879 G>A maps to NM_001995.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:131312358 G>A maps to NM_001009185.1 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr16:20563465 C>T maps to NM_182617.3 K298K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5772-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:20797542 C>T maps to NM_202000.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:24994193 G>A maps to NM_032501.2 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr20:33514746 C>T maps to NM_001076552.2 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr12:81647349 T>C maps to NM_024560.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:229568582 G>A maps to NM_001100.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr7:5568827 G>A maps to NM_001101.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:5568089 G>A maps to NM_001101.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:56777945 G>A maps to NM_001017992.2 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr15:35087000 G>A maps to NM_005159.4 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr17:79478955 G>A maps to NM_001614.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr19:8808028 G>A maps to NM_178525.3 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr14:69341704 G>A maps to NM_001130004.1 R872R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:69341599 C>T maps to NM_001130004.1 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:69345204 G>A maps to NM_001130004.1 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:236900480 G>A maps to NM_001103.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:236902769 C>T maps to NM_001103.2 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39218656 C>T maps to NM_004924.3 N803N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:114709087 A>T maps to NM_005721.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:100613795 G>A maps to NM_022496.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr23:127185763 G>A did not map to a codon.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr23:127185902 G>A did not map to a codon.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr23:127185961 T>G did not map to a codon.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr23:127185962 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:127185974 G>T did not map to a codon.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr1:2939176 C>T maps to NM_080431.4 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr2:158395159 C>A maps to NM_145259.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr2:148683678 T>A maps to NM_001616.3 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr11:67410242 G>A maps to NM_080658.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:84228123 G>A maps to NM_139174.3 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:127737878 G>A maps to NM_003474.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr10:127730775 G>A maps to NM_021641.3 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:127730739 C>T maps to NM_021641.3 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:155028576 C>T maps to NM_207197.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:9637267 C>T maps to NM_003183.4 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr8:39495170 G>A maps to NM_014237.2 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr8:39525629 C>T maps to NM_014237.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:156957867 C>T maps to ENST00000430702 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr8:39624424 G>A maps to NM_001464.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr8:39624554 G>C maps to NM_001464.3 S440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr8:39624517 G>A maps to NM_001464.3 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:70990157 A>G maps to NM_003814.4 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:70991495 C>T maps to NM_003814.4 W43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr8:24199260 C>T maps to NM_014265.4 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:175897498 G>T maps to NM_014269.4 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr4:175897857 C>T maps to NM_014269.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:175897509 G>A maps to NM_014269.4 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr1:120438878 G>A maps to NM_021794.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:24350742 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr8:38880723 G>A maps to NM_003816.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr8:38880739 G>A maps to NM_003816.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:38874761 G>A maps to NM_003816.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr8:24254908 G>A maps to NM_014479.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr21:28210278 G>A maps to NM_006988.3 F841F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:28209960 G>A maps to NM_006988.3 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr19:8668747 G>A maps to NM_030957.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:8670019 C>A maps to NM_030957.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr19:8651509 G>A maps to NM_030957.2 R779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr19:8665931 G>A maps to NM_030957.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr5:33630977 C>T maps to NM_030955.2 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:72511283 C>T maps to NM_139155.2 Y829Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr10:72498707 C>T maps to NM_139155.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:72462204 C>T maps to NM_139155.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:72489063 C>T maps to NM_139155.2 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:130343427 C>T maps to NM_139055.2 C855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:130332479 G>A maps to NM_139055.2 E449E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:5303542 G>A maps to NM_139056.2 Q984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:5239962 C>T maps to NM_139056.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:5235198 C>T maps to NM_139056.2 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:5303788 C>T maps to NM_139056.2 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B2-01A-12D-A32B-08 chr15:100537661 G>A maps to NM_139057.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MK-01A-11D-A364-08 chr15:100594118 G>A maps to NM_139057.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:100802622 C>T maps to NM_139057.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr5:128994428 A>G maps to NM_133638.3 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr5:178634657 G>A maps to NM_014244.4 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:43777765 A>G maps to ENST00000389420 C1489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr12:43944935 G>A maps to ENST00000389420 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:43826456 G>A maps to ENST00000389420 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr4:73186557 T>A maps to NM_014243.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:73169735 C>T maps to NM_014243.1 S774S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr21:28327145 G>A maps to NM_007038.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr21:28327085 G>A maps to NM_007038.3 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr21:28338098 C>T maps to NM_007038.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr21:28306853 C>T maps to NM_007038.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:64629881 G>T maps to NM_197941.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DK-01A-11D-A377-08 chr15:79058841 G>A maps to ENST00000258883 A1137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr11:130281312 G>A maps to NM_007037.4 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:64554180 G>A maps to NM_182920.1 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:64532490 G>A maps to NM_182920.1 P1669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:64617535 G>A maps to NM_182920.1 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr9:18504837 C>T maps to NM_001040272.4 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:18622251 C>T maps to NM_001040272.4 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:18681925 C>T maps to NM_001040272.4 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:18887910 G>A maps to NM_001040272.4 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr7:939747 C>G maps to NM_006869.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:154560616 G>A maps to ENST00000292205 R1044R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:154557715 G>A maps to ENST00000292205 D1183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:46624622 C>A maps to NM_015833.3 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:1405753 C>T maps to NM_018702.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:140373322 C>T maps to NM_052853.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:140373594 G>A maps to NM_052853.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41209497 G>A maps to NM_024876.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145616625 G>A maps to NM_174922.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:45744118 C>A maps to NM_021116.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr1:167823645 A>C maps to NM_018417.4 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr1:167871269 G>A maps to NM_018417.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:167793913 T>C maps to NM_018417.4 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr5:7414747 G>A maps to NM_020546.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr14:24789052 G>A maps to NM_139247.3 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr14:24793575 C>T maps to NM_139247.3 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr14:24791403 G>A maps to NM_139247.3 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr14:24791910 G>A maps to NM_139247.3 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr3:123049809 C>T maps to NM_183357.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:49169814 C>T maps to NM_015270.3 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr12:49170257 G>A maps to NM_015270.3 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:49165678 G>A maps to NM_015270.3 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:49172004 G>A maps to NM_015270.3 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr16:50341043 C>T maps to NM_001114.3 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr8:131792812 G>A maps to NM_001115.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:132051760 G>A maps to NM_001115.2 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr8:131848632 G>A maps to NM_001115.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr16:4042211 C>T maps to NM_001116.3 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:4016804 G>A maps to NM_001116.3 D1011D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr2:70890787 G>A maps to NM_001185054.1 N650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:100128603 T>C maps to NM_001102470.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:100334310 C>T maps to NM_000673.4 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr18:77896568 T>C maps to NM_014913.3 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:112045901 G>A maps to NM_020683.6 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr8:26628172 G>A maps to ENST00000356368 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr8:26623612 A>G maps to NM_033304.2 H441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:3769055 G>A maps to NM_000683.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr5:148206405 C>T maps to NM_000024.5 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:148207350 T>G maps to NM_000024.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:67052767 G>A maps to NM_001619.3 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:105208269 C>T maps to NM_199165.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr7:44146385 G>A maps to NM_001129.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:19653145 T>C maps to NM_001114176.1 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr4:7802210 C>T maps to NM_001134647.1 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:148699200 C>A maps to NM_152406.2 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:148037364 G>A did not map to a codon.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr23:148037364 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr23:148069053 G>T did not map to a codon.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:147733565 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:147967509 T>C did not map to a codon.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr23:147744150 C>G did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:100170917 G>A maps to NM_001025108.1 N1163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:100623892 C>G maps to NM_001025108.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:12351344 C>T maps to NM_006796.2 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr18:12370899 T>C maps to NM_006796.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr4:74351739 C>T maps to NM_001133.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr10:88769149 C>T maps to NM_133447.1 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:58123440 G>A maps to NM_001122772.1 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:51748528 C>T maps to NM_001077665.2 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr10:51225501 G>A maps to ENST00000425119 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr15:86838595 G>A maps to NM_152336.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr11:47712124 C>T maps to ENST00000357610 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr2:228388505 C>T maps to NM_001135187.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr7:141315345 G>T maps to NM_018238.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr7:141351366 G>A maps to NM_018238.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:100346234 C>T maps to ENST00000311030 R596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139571063 G>A maps to NM_006412.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr21:45379681 G>A maps to NM_001037553.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:6605239 C>T maps to NM_018361.3 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr2:178386035 C>T maps to NM_003659.3 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr2:178402826 A>G maps to NM_003659.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:230845753 G>A maps to NM_000029.3 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr3:148459292 C>A maps to NM_032049.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr23:115304402 C>T did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:247014375 G>C maps to ENST00000428671 A1682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr1:27874813 C>T maps to NM_001029882.2 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr6:135787208 G>A maps to NM_017651.4 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:135639718 G>A maps to NM_017651.4 R1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:135769460 G>A maps to NM_017651.4 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:62284329 C>A maps to NM_001620.1 V5853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:62301276 G>A maps to NM_001620.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr11:62289689 T>A maps to NM_001620.1 K4067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62284494 C>T maps to NM_001620.1 T5798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62288745 C>T maps to NM_001620.1 K4381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62289162 G>A maps to NM_001620.1 G4242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62291031 G>A maps to NM_001620.1 G3619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr14:105414188 A>T maps to NM_138420.2 I2533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr14:105414143 G>A maps to NM_138420.2 D2548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr14:105421874 G>A maps to NM_138420.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr14:105416336 A>C maps to NM_138420.2 T1817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr14:105420974 C>A maps to NM_138420.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr14:105409472 G>T maps to NM_138420.2 A4105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr14:105418649 G>A maps to NM_138420.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr14:105418826 G>A maps to NM_138420.2 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:105410918 G>A maps to NM_138420.2 D3623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:105413600 C>T maps to NM_138420.2 G2729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:427995 G>A maps to NM_020731.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr5:432966 T>C maps to NM_020731.3 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:424016 C>T maps to NM_020731.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:186331025 C>T maps to ENST00000273784 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr16:31539919 G>T maps to NM_016633.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr12:8758039 C>T maps to NM_020661.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr10:71877571 C>A maps to NM_032797.5 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:71883672 G>A maps to NM_032797.5 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:21330572 C>T maps to NM_144704.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:106969053 T>A maps to NM_001624.2 L916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr1:159035789 A>T maps to NM_004833.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr1:4832546 G>A maps to NM_018836.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr1:4832549 G>A maps to NM_018836.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:130630298 G>A maps to ENST00000223836 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:130634179 G>A maps to ENST00000223836 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:55193499 G>A maps to ENST00000427138 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr6:151671703 C>T maps to NM_005100.3 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:119048758 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr23:49955713 T>A did not map to a codon.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr23:49958073 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:33015925 G>A maps to NM_004274.4 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:131490306 A>G maps to ENST00000431975 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr7:91631336 A>G maps to NM_005751.4 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr7:91691588 C>T maps to NM_005751.4 G1922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:91726085 C>T maps to NM_005751.4 N3271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr7:91667794 A>G maps to NM_005751.4 G1467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:91670088 C>T maps to NM_005751.4 Y1598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:88385620 C>T maps to NM_018064.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:117103925 C>T maps to NM_030767.4 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:117106078 G>A maps to NM_030767.4 H1222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr7:134252992 G>A maps to ENST00000418096 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr10:5011015 C>T maps to NM_001353.5 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:5008274 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:4875567 C>A maps to NM_001040177.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:19632607 C>T maps to NM_003689.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr1:19597013 G>T maps to NM_201252.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:19600454 G>A maps to NM_201252.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr19:40745987 G>A maps to NM_001626.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:40762905 G>T maps to NM_001626.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52239989 C>A maps to ENST00000441729 C329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr23:55039949 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr9:75567853 A>T maps to NM_000689.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr15:101425524 A>C maps to NM_000693.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr9:38396791 G>A maps to NM_000692.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr3:125824674 G>A maps to ENST00000273450 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:105462662 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:112237729 G>A maps to NM_000690.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr17:19559758 G>A maps to NM_001031806.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67431902 C>T maps to NM_001031615.1 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr14:74537997 T>C maps to NM_005589.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:104192138 G>A maps to NM_000035.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:95530490 A>G maps to NM_144988.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:101980872 G>A maps to NM_033087.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr14:78174326 G>A maps to NM_006020.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:109526136 G>A maps to NM_001145375.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:102100194 C>T maps to NM_017621.3 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr2:3744988 C>T maps to ENST00000403787 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr2:73828484 C>T maps to NM_015120.4 D4011D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr2:73717896 T>G maps to NM_015120.4 Y2936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L2-01A-31D-A41K-08 chr2:73717485 T>A maps to NM_015120.4 V2799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr17:4535297 C>T maps to NM_001140.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:45939257 C>T maps to NM_000698.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr2:233323609 G>A maps to NM_001631.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:233323450 C>T maps to NM_001631.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr18:56246186 C>T maps to NM_052947.3 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr18:56246843 C>T maps to NM_052947.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:85410591 C>T maps to NM_020778.4 R1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr15:85403129 T>G maps to NM_020778.4 P1565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr15:85403111 C>T maps to NM_020778.4 T1559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:85384033 C>T maps to NM_020778.4 C710C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr15:85402607 G>T maps to NM_020778.4 E1520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:21903984 C>T maps to NM_000478.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr2:233271621 G>T maps to NM_031313.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:233271615 C>A maps to NM_031313.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:202625666 C>T maps to NM_020919.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:46724744 C>A maps to NM_147129.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:46721967 G>A maps to NM_147129.3 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr3:46713450 C>T maps to NM_147129.3 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:203839188 G>A maps to NM_024744.14 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr1:110607210 G>A maps to NM_006492.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:110603474 G>A maps to NM_006492.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr11:44289105 G>A maps to NM_021926.3 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:34005918 G>A maps to NM_001167595.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:116835295 C>T maps to NM_001633.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr11:46569884 G>A maps to ENST00000458649 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:2579488 C>T maps to NM_001145815.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr16:56398014 G>A maps to NM_001144.4 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr12:53819284 A>G maps to NM_020547.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:53818595 C>T maps to NM_020547.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr12:47472524 C>T maps to NM_001143668.1 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:49755884 G>A maps to NM_198722.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49755425 C>T maps to NM_198722.2 E491E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr3:49756031 G>A maps to NM_198722.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr23:112058795 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:112024247 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:112034008 C>T did not map to a codon.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:112022740 T>C did not map to a codon.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr11:94533201 G>T maps to NM_130847.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:10503680 G>A maps to NM_000480.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:104117886 A>G maps to NM_020978.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:2740186 C>T maps to NM_133463.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:2752067 C>T maps to NM_133463.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr7:2752463 C>T maps to NM_133463.1 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:112604724 G>A maps to NM_022662.2 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr4:25393992 G>T maps to ENST00000510092 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:25382010 C>T maps to ENST00000510092 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:213178539 C>T maps to NM_144567.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr8:6360775 C>T maps to NM_001147.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr20:861825 C>T maps to NM_015985.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:896758 G>A maps to NM_015985.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr9:129870587 G>T maps to NM_012098.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr11:101775572 A>G maps to NM_178127.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:41572580 G>A maps to ENST00000415018 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr8:41529903 G>A maps to ENST00000415018 T1688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:41566426 G>A maps to ENST00000415018 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:41583416 G>A maps to ENST00000415018 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr8:41559077 C>A maps to ENST00000415018 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr4:114278435 A>T maps to NM_001148.4 K2888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:114275161 C>T maps to NM_001148.4 D1796D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:114290837 C>T maps to NM_001148.4 P3829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr4:114214648 C>T maps to NM_001148.4 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr4:114275608 G>A maps to NM_001148.4 T1945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr4:114279595 C>A maps to NM_001148.4 P3274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr4:114251468 C>T maps to NM_001148.4 R990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr4:114274942 A>G maps to NM_001148.4 A1723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:114238871 C>A maps to NM_001148.4 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:114276469 G>A maps to NM_001148.4 K2232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr10:61827717 G>A maps to NM_020987.2 A4098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:61819477 G>A maps to ENST00000503366 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:61829571 G>A maps to NM_020987.2 S3689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:61844448 G>A maps to NM_020987.2 R1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:61868694 G>A maps to NM_020987.2 C1022C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr2:190554475 T>G maps to NM_144708.3 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr2:190554682 T>C maps to NM_144708.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:190569830 G>A maps to NM_144708.3 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:190603352 T>C maps to NM_144708.3 V1215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:190606143 G>A maps to NM_144708.3 R1259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr17:54558082 G>A maps to NM_153228.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:54526455 C>T maps to NM_153228.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr17:54554925 C>T maps to NM_153228.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:54554979 C>A maps to NM_153228.2 C638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:54559799 C>T maps to NM_153228.2 D728D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr5:14711383 C>T maps to NM_054027.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr5:139887387 T>A maps to ENST00000253810 G1190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr5:139905803 G>A maps to ENST00000253810 K1572K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:139818199 C>T maps to ENST00000253810 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:139865208 T>C maps to ENST00000253810 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr19:17394283 T>C maps to NM_152363.4 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:133331648 G>A maps to NM_015114.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr12:133304673 C>A maps to NM_015114.1 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:241468860 G>A maps to ENST00000401804 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:241465185 C>T maps to ENST00000401804 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr7:16640445 G>A maps to NM_020319.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:89350060 G>A maps to NM_013275.4 D963D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:89348869 G>A maps to NM_013275.4 S1360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:89350882 G>A maps to NM_013275.4 H689H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:9281096 C>T maps to NM_015208.3 N2054N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:27939516 C>T maps to NM_152345.4 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:74005374 T>G maps to NM_032217.3 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr4:74010531 A>C maps to NM_032217.3 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:74019645 C>T maps to NM_032217.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:97506645 G>A maps to NM_144994.7 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr10:27381414 T>A maps to NM_014915.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MG-AAMC-01A-11D-A41K-08 chr19:33149849 C>T maps to NM_032139.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:33134216 G>A maps to NM_032139.2 Y227Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:33135304 G>A maps to NM_032139.2 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:33137497 C>T maps to NM_032139.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr3:15736274 T>A maps to NM_015199.3 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr10:37508446 T>G maps to ENST00000374660 Y1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr10:37430946 G>A maps to ENST00000374660 W318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:37430805 G>A maps to ENST00000374660 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:14757888 C>G maps to NM_001145029.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr18:14850218 T>A maps to NM_001145029.1 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr5:94022424 T>G did not map to a codon.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr5:94027887 C>T maps to NM_032290.3 D874D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr1:145561190 G>A maps to NM_144698.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr2:97779508 C>A maps to NM_001164315.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:97877446 G>A maps to NM_001164315.1 T1146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:132150755 C>T maps to NM_175873.4 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:197870469 A>G maps to NM_001195144.1 C765C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:197878289 G>A maps to NM_001195144.1 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr12:56638933 C>T maps to NM_173595.3 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:56641861 G>A maps to NM_173595.3 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:55472068 C>T maps to NM_024669.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr5:55422828 C>T maps to NM_024669.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr12:100166697 A>G did not map to a codon.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr12:99837458 G>A maps to NM_152788.3 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr16:4780009 C>T maps to NM_133450.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:101552590 G>A maps to ENST00000375018 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:101540676 G>A maps to ENST00000375018 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:70031719 G>A maps to NM_018043.5 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:70009406 C>T maps to NM_018043.5 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr12:101505339 G>A did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr12:101493354 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr11:22249074 G>A maps to NM_213599.2 E197E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr2:242138765 C>T maps to NM_001001891.3 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr2:242128088 C>G maps to NM_001001891.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr15:69080171 T>C maps to NM_006305.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr15:90348338 G>A maps to NM_001150.2 Y289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:90348600 C>T maps to NM_001150.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:80954650 G>T maps to NM_001145794.1 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr10:46113585 G>C did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:124705462 G>A maps to NM_001003954.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr15:60641329 T>A maps to NM_001002858.2 K320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:70047881 G>T maps to NM_001153.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:122599623 G>A maps to NM_001154.3 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr10:75139866 G>A maps to NM_004034.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:150960777 A>G maps to NM_003568.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr17:41004622 C>G maps to NM_003734.2 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr2:201499583 A>G maps to NM_001159.3 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:71803537 C>T maps to ENST00000423132 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:24031219 G>A maps to NM_003917.2 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr14:24035555 C>T maps to NM_003917.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:16345075 C>T maps to NM_001130524.1 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:50302914 G>T maps to NM_014203.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50285951 C>T maps to NM_014203.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50302733 C>T maps to NM_014203.2 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:988649 C>T maps to ENST00000332231 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr11:994172 G>A maps to ENST00000332231 E629E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:33966625 C>A maps to NM_001030006.1 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr3:183901337 C>T maps to ENST00000411763 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:2116220 C>T maps to ENST00000355272 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:75888896 G>A maps to NM_207012.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr9:72131100 C>T maps to NM_001163.3 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr9:72131394 G>A maps to NM_001163.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr9:72131721 G>A maps to NM_001163.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr9:72131765 G>A maps to NM_001163.3 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:72047550 G>A maps to NM_001163.3 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:72067035 A>G did not map to a codon.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr15:29346407 C>T maps to NM_005503.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr10:26785234 T>C maps to NM_019043.3 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr10:26825136 A>G maps to NM_019043.3 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:139939990 G>A maps to ENST00000354402 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr5:112175906 C>G maps to NM_001127510.2 S1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr5:112174657 C>T maps to NM_001127510.2 Q1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr5:112151260 C>T maps to NM_001127510.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr5:112175855 T>G maps to NM_001127510.2 L1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr5:112175489 C>A maps to NM_001127510.2 S1400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr5:112174630 C>T maps to NM_001127510.2 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:1465594 C>T maps to NM_005883.2 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr19:1465240 C>T maps to NM_005883.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr11:43345104 A>C maps to NM_001142930.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr2:68765197 C>T maps to NM_173545.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:68740262 C>T maps to NM_173545.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:68794511 G>A maps to NM_173545.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:130010332 C>T maps to NM_001642.2 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr1:156563207 G>A maps to ENST00000446584 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:116692050 C>T maps to NM_000482.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr2:21234066 A>G maps to NM_000384.2 H1891H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr2:21233705 G>A maps to NM_000384.2 R2012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr2:21228378 G>A maps to NM_000384.2 P3787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr2:21249773 A>G maps to NM_000384.2 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr22:39421245 C>T maps to NM_152426.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr22:39439010 T>G maps to NM_145298.5 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr22:39477230 C>T maps to NM_021822.3 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr1:183617688 A>T maps to NM_203454.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr11:116701558 C>A maps to ENST00000360377 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr19:45445566 G>T maps to NM_001646.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr19:45411081 G>T maps to NM_000041.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:36587467 G>A maps to ENST00000332987 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr22:36123053 C>T maps to NM_030642.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:23876822 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:23876769 C>T did not map to a codon.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr17:58529352 A>G maps to NM_006380.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:58525051 G>A maps to NM_006380.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:241631738 G>A maps to ENST00000429564 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:50349300 G>A maps to NM_000486.5 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:50349237 C>T maps to NM_000486.5 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:115327975 C>T did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr15:35185965 G>C maps to NM_014691.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr15:35207357 C>T maps to NM_014691.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr23:66905871 G>A did not map to a codon.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr23:66905905 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:47428237 C>T did not map to a codon.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr23:47428272 G>A did not map to a codon.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr11:72420925 G>A maps to NM_001040118.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:36130283 T>G maps to NM_015230.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr4:36130196 G>A maps to NM_015230.2 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:141036141 G>A maps to NM_022481.5 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr8:143694681 G>A maps to NM_015193.3 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118461127 G>A maps to ENST00000359415 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr1:228284841 C>T maps to NM_001024228.1 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr22:43204770 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:47649585 C>T maps to NM_006420.2 Y1736Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:148886178 C>T maps to NM_024605.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:148876465 G>T did not map to a codon.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr2:144381720 C>T maps to NM_018460.3 D341D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:24953339 C>T maps to NM_001006634.1 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr11:110450381 C>T maps to NM_020809.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr10:24909692 C>T maps to NM_020824.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr4:86916228 G>A maps to NM_001025616.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:86916273 C>T maps to NM_001025616.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:142311641 G>A maps to NM_015071.4 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr18:6896511 G>T maps to ENST00000400091 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:6896556 C>A maps to ENST00000400091 S654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:161022537 T>C maps to NM_001025598.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr1:161019031 G>A maps to NM_001025598.1 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr3:119133913 A>C maps to NM_020754.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr3:119134360 C>T maps to NM_020754.2 C1195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:128844093 C>A maps to NM_001142685.1 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr11:128844289 T>C maps to NM_001142685.1 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr19:36278973 C>T maps to ENST00000007510 Y1169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr19:36275139 G>A maps to ENST00000007510 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr23:130220377 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr23:130217749 T>A did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:145773443 G>A maps to NM_025251.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr8:145773233 G>A maps to NM_025251.1 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr23:153187218 C>A did not map to a codon.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr14:32561296 A>G maps to NM_001030055.1 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr14:32560135 A>G maps to NM_001030055.1 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr23:11204544 T>C did not map to a codon.
Multiple mappings detected for codon TCGA-G9-6377-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr8:1900968 C>T maps to ENST00000398564 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:17958925 C>T maps to NM_018125.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:17952503 G>A maps to NM_018125.3 K457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:156937787 G>A maps to NM_198236.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156918208 G>A maps to NM_198236.1 N669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:120298823 G>A maps to NM_015313.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr17:8215725 G>A maps to NM_173728.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr11:73022673 G>A maps to NM_014786.3 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:73020417 T>C maps to NM_014786.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:73076577 C>T maps to NM_014786.3 D1898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:7509123 G>A maps to NM_001130955.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:7518422 C>T maps to NM_001130955.1 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:16534047 G>A maps to NM_153213.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:16534594 A>G maps to NM_153213.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr1:16532161 G>A maps to NM_153213.3 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16534186 G>A maps to NM_153213.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr4:106473930 C>T maps to ENST00000420470 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:144060433 C>A maps to NM_005435.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:144070323 C>T maps to NM_005435.3 R1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:135790918 C>T did not map to a codon.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr23:62857908 C>T did not map to a codon.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr23:62863889 T>C did not map to a codon.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr1:27087547 C>T maps to NM_006015.4 Q708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:27106760 A>G maps to NM_006015.4 K2124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:27101586 G>A maps to NM_006015.4 S1623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr6:157528682 G>A maps to ENST00000367148 S2176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr6:157527452 C>T maps to ENST00000367148 D1766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:157150549 C>T maps to ENST00000367148 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DK-01A-11D-A377-08 chr6:157502128 G>A maps to ENST00000367148 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:157469869 C>T maps to ENST00000367148 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:157527545 C>T maps to ENST00000367148 S1797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr12:46211600 C>T maps to NM_152641.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr12:46244875 G>A maps to NM_152641.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr19:964320 G>A maps to NM_005224.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:235416113 G>A maps to NM_016374.5 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr1:235338685 T>G maps to NM_016374.5 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:97216924 C>T maps to NM_212481.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr3:49004608 C>T maps to NM_006321.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:50204663 G>A maps to NM_138450.5 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr17:79650771 C>G maps to NM_001040025.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr2:235405079 T>A maps to ENST00000339728 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:18962968 T>C maps to NM_178815.3 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr6:109215690 G>A maps to NM_032131.4 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr10:23287301 G>A maps to NM_173081.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:23292174 G>A maps to NM_173081.3 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:31473605 G>T maps to ENST00000408912 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr16:31473497 G>A maps to ENST00000408912 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:31475816 C>T maps to ENST00000408912 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr16:31476479 G>T maps to NM_024742.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19154808 C>T maps to ENST00000392336 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:232196542 C>T maps to ENST00000359743 D604D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:232209766 C>T maps to ENST00000359743 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:100911831 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:100912111 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:101858623 A>G did not map to a codon.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr10:124214266 G>T maps to NM_001099667.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:80866542 A>T maps to NM_014862.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr12:27542199 C>A maps to NM_020183.3 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:27533278 T>C maps to NM_020183.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:127637402 C>T maps to NM_030978.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr3:169486065 A>G maps to NM_032487.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr3:35785413 C>T maps to ENST00000458225 N664N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:35770906 G>C maps to ENST00000458225 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:4902801 G>A maps to NM_001080523.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:2838676 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:2867522 G>A did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr23:2876455 A>G did not map to a codon.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr23:2856152 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:3002367 G>A did not map to a codon.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr23:3002433 A>G did not map to a codon.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr23:2990115 C>A did not map to a codon.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr23:2936616 C>T did not map to a codon.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr5:94927204 T>C maps to NM_198150.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:94903714 T>C maps to NM_198150.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:19959483 G>T maps to NM_001670.2 S902S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:19969196 C>A maps to NM_001670.2 G145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:19969539 C>T maps to NM_001670.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:122944220 G>A maps to NM_024769.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:131249204 C>G maps to NM_018482.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:131092212 G>A maps to NM_018482.2 N859N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:131136320 A>G maps to NM_018482.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr8:131130462 G>A maps to NM_018482.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:9484929 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:9528610 C>T maps to NM_003887.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr1:23782630 G>A maps to NM_017707.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:239353280 C>T maps to NM_001040445.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:63444280 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:63444982 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr7:123269121 T>C maps to NM_080928.3 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr1:76397715 G>A maps to NM_080868.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:76397715 G>A maps to NM_080868.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr2:237172856 G>A maps to NM_212556.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr14:94420792 G>A maps to ENST00000434324 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:177136780 C>T maps to NM_080874.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr9:132400167 C>T maps to NM_017873.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr12:48543214 G>A maps to NM_024095.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:48543493 G>A maps to NM_024095.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr23:15270502 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr6:101098515 T>C maps to NM_006828.2 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr17:7012079 G>A maps to NM_080912.2 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr1:155451979 A>T maps to ENST00000368346 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:155429592 G>C maps to ENST00000368346 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr1:155449428 G>A maps to ENST00000368346 Q1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr1:155491262 T>C maps to ENST00000368346 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:155313528 G>A maps to ENST00000368346 D2667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr1:155348169 A>T maps to ENST00000368346 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:65553836 C>T maps to NM_000048.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr23:1755353 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:1743282 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr23:1748781 T>G did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:1561135 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:1546861 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:12856476 C>T maps to NM_004317.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr7:97488603 G>A maps to NM_183356.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:190532518 G>A maps to NM_019048.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:3379479 A>G maps to NM_000049.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:197104364 G>C maps to NM_018136.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr1:197111886 T>A maps to NM_018136.4 K499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr1:197061107 G>A maps to NM_018136.4 Q3125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:95228838 G>A maps to NM_017680.4 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:70188205 C>T maps to NM_152792.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:79954526 G>A maps to ENST00000306729 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79941441 C>T maps to ENST00000306729 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62156673 C>T maps to NM_025080.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr3:130743333 G>A maps to ENST00000514044 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr2:96795626 C>T maps to NM_001002036.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr1:176852022 G>A maps to ENST00000281881 R1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr20:31023727 G>A maps to ENST00000375687 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:31021260 C>T maps to ENST00000375687 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31022608 G>A maps to ENST00000375687 P698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr2:25982349 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:31324983 C>T maps to NM_030632.1 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:1459696 C>T maps to NM_018188.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:1421967 C>T maps to NM_031921.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr1:1389855 T>G maps to NM_001039211.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr10:123658409 G>C maps to NM_007041.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:123600628 C>T maps to NM_001001976.1 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr22:39917542 A>G maps to NM_182810.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50436129 C>T maps to NM_001193646.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:161789583 G>A maps to NM_007348.2 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr6:32083516 C>T maps to NM_004381.4 *704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32087656 T>G maps to NM_004381.4 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr12:53917099 G>A maps to NM_001130059.1 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr12:14628822 G>T did not map to a codon.
Sequencing variant TCGA-EJ-AB20-01A-12D-A41K-08 chr5:81548457 G>A maps to NM_031482.4 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:81354374 C>G maps to NM_031482.4 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr2:234178653 G>A maps to ENST00000392018 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64665160 G>A maps to ENST00000421419 H1685H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64678410 G>A maps to ENST00000421419 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64678616 C>T maps to ENST00000421419 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:96800091 G>A maps to NM_018036.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:96768373 C>T maps to NM_018036.5 S1703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:96829258 G>A maps to NM_018036.5 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr23:107396936 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr6:106764040 G>A maps to NM_004849.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr2:220087402 G>C maps to NM_024085.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:294383 C>T maps to ENST00000409479 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr2:216198160 G>C maps to NM_004044.6 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr11:108199782 T>C maps to NM_000051.3 S2375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr11:108224577 C>G maps to NM_000051.3 G2919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr16:81078136 C>T maps to NM_015251.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:81078145 C>T maps to NM_015251.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr15:26026297 G>A maps to NM_024490.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:25953222 G>A maps to NM_024490.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:25932909 G>A maps to NM_024490.3 H1077H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:25981213 A>G maps to NM_024490.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr15:25958881 G>A maps to NM_024490.3 I761I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr15:25959330 T>G maps to NM_024490.3 R612R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr5:160047582 G>A maps to NM_025153.2 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:160033838 C>A maps to NM_025153.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr5:160114976 T>C maps to NM_025153.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr5:160061405 G>A maps to NM_025153.2 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr4:47527618 G>T maps to NM_020453.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:113512220 G>A maps to NM_032189.3 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:182586926 C>T maps to NM_014616.1 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:182587058 C>T maps to NM_014616.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr23:138856995 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:138820131 G>A did not map to a codon.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr19:19766137 G>A maps to NM_020410.2 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19762590 C>A maps to NM_020410.2 G748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr1:17314695 G>A maps to NM_022089.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:17322787 G>A maps to NM_022089.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:194126842 C>T maps to NM_024524.3 E1162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr3:194146083 A>G maps to NM_024524.3 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr3:193183887 T>G maps to NM_032279.2 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:193052823 A>G maps to NM_198505.2 C336C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr1:160093052 C>T maps to NM_000702.3 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr1:160099087 T>C maps to NM_000702.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:160098443 G>A maps to NM_000702.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:160134024 G>A maps to NM_144699.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:160134087 C>T maps to NM_144699.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr12:110765383 T>A maps to NM_170665.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:90049657 G>A maps to ENST00000428670 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr3:10417119 C>T maps to NM_001001331.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:10392201 G>A maps to NM_001001331.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:152807164 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:152821636 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr23:152815040 G>A did not map to a codon.
Sequencing variant TCGA-V1-A9OA-01A-11D-A41K-08 chr23:152826169 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:152807866 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:152807869 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:152815020 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:152815039 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:203690538 G>A did not map to a codon.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr1:203677048 C>T maps to NM_001001396.1 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:130698120 G>T maps to NM_001001486.1 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:84438756 G>A maps to ENST00000416219 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:84456039 C>T maps to ENST00000416219 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr12:57032139 T>C maps to NM_001686.3 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:7844329 C>A maps to NM_001001973.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:73035038 A>G maps to NM_006356.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr23:40457948 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr7:138437473 G>A maps to NM_130840.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:138455971 G>A maps to NM_130840.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr1:44442866 G>C maps to NM_004047.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67472891 G>A maps to NM_004691.4 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:113514786 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr2:10915196 T>A maps to NM_001039362.1 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:77301978 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:77264644 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:52548293 G>A maps to NM_000053.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr1:154305092 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr1:154309882 G>A maps to NM_020452.3 E332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:154321479 G>A maps to NM_020452.3 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:1796999 C>T maps to NM_138813.2 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr15:50212486 C>A maps to NM_024837.2 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:50244192 C>A maps to NM_006045.1 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:50226671 G>A maps to NM_006045.1 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr3:142204016 A>T maps to NM_001184.3 G2062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:142180884 T>C maps to NM_001184.3 R2363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr3:142272701 C>A maps to NM_001184.3 E833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:3520964 G>A maps to NM_139321.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:76940432 A>C did not map to a codon.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr23:76891437 A>G did not map to a codon.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr23:76845371 A>C did not map to a codon.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr23:76855226 C>A did not map to a codon.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr6:16328223 G>A maps to NM_000332.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr12:111954060 C>A maps to NM_002973.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr14:92548748 C>A maps to ENST00000359819 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr23:13337264 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:63898513 G>A maps to NM_001177387.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46B-01A-31D-A257-08 chr3:63981654 C>T maps to NM_001177387.1 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr7:70252228 C>A maps to NM_015570.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr7:70228265 C>T maps to NM_015570.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:63543827 A>G maps to NM_000706.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:63543656 G>A maps to NM_000706.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:69458061 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr23:69261785 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr17:63553973 C>G maps to NM_004655.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:63554078 G>A maps to NM_004655.3 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41737136 G>A maps to NM_021913.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr19:41745621 C>T maps to NM_021913.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99565868 G>A maps to NM_001185.3 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr19:829579 C>T maps to NM_001700.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr1:235647822 G>A maps to ENST00000366599 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr6:33245990 G>A maps to NM_003782.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:33246263 C>A maps to NM_003782.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr19:17919011 C>T maps to NM_014256.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41931654 G>A maps to NM_198540.2 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:58022501 G>A maps to NM_001478.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr12:58020595 G>A maps to NM_001478.3 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:47247083 C>T maps to NM_153446.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:380293 C>T maps to NM_178537.4 D906D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:376472 C>T maps to NM_178537.4 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:380446 T>C did not map to a codon.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr11:373291 G>C did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr18:29218611 C>A maps to NM_004775.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr9:104133251 G>A maps to NM_001701.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:42622767 C>T maps to NM_012105.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:90661074 G>A maps to NM_001170794.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:57048804 T>C maps to NM_004282.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr21:11098731 C>T maps to NM_181704.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr21:11049591 C>T maps to NM_182482.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:11058295 C>T maps to NM_182482.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:79412648 C>T maps to ENST00000436173 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:79426158 C>T maps to ENST00000436173 Y1895Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79409832 C>T maps to ENST00000436173 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr8:143558526 C>T maps to NM_001702.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr8:143565393 G>A maps to NM_001702.2 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:32196526 G>T maps to NM_001703.2 P1418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:32207729 G>A maps to NM_001703.2 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:69758170 C>T maps to NM_001704.2 N734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr6:69349085 T>G maps to NM_001704.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr22:38494423 G>A maps to NM_025045.4 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:33543082 A>G maps to ENST00000360661 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:102946625 T>C maps to NM_017935.4 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88061087 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52437771 C>T maps to NM_004656.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:215645850 G>A maps to NM_000465.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr1:91182527 C>A maps to NM_020063.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:17275930 C>T maps to NM_006317.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr9:134366822 A>T maps to NM_013318.3 P2079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:134351101 C>T maps to NM_013318.3 R1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:171556248 C>T maps to ENST00000392078 T2619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:31608179 C>T maps to ENST00000404765 W1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr6:31668721 G>A maps to ENST00000375842 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:35255347 C>T maps to NM_013448.2 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:57003984 G>A maps to NM_013449.3 N600N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr2:160289577 A>G maps to NM_013450.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:160182234 C>T maps to NM_013450.2 L2046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr2:160193563 C>A maps to NM_013450.2 G1895G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr11:27077077 T>A maps to NM_003986.2 L34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:123664109 C>T maps to NM_152618.2 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:123664603 C>T maps to NM_152618.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:123665161 G>A maps to NM_152618.2 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr15:73029879 G>A maps to NM_033028.3 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr1:156618649 C>T maps to NM_021948.3 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:94049650 G>A maps to NM_003567.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:115123931 A>C maps to NM_005872.2 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr19:49299744 G>A maps to NM_001190.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49303236 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49309971 A>G maps to NM_001190.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:165548401 C>T maps to NM_000055.2 W140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr16:31122507 C>T maps to NM_005881.2 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:31122644 C>T maps to NM_005881.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:31123312 C>T maps to NM_005881.2 D353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr2:60689482 G>A maps to NM_022893.3 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr2:60687904 G>A maps to NM_022893.3 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:99641822 C>T maps to NM_138576.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr15:52402107 G>A maps to NM_020396.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:45260308 G>A maps to NM_005178.4 P185P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-5518-01A-01D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:187451334 G>A maps to ENST00000449623 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:147084928 C>T maps to NM_004326.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118772813 C>T maps to NM_182557.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118773617 C>A did not map to a codon.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr6:136594275 C>T maps to NM_014739.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr6:136599813 G>A maps to NM_014739.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:136590579 A>G maps to NM_014739.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:81298345 G>A maps to NM_017429.2 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr23:39914705 A>G did not map to a codon.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr23:39911628 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr23:39933374 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:39930265 G>T did not map to a codon.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr23:129155088 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:129148509 G>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:129146575 G>C did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:129147471 G>C did not map to a codon.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr23:129155026 G>C did not map to a codon.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr23:129149432 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:27722531 C>A maps to NM_001143809.1 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr11:27679583 T>C maps to NM_001143810.1 Q258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr6:107390675 G>A maps to NM_001080450.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:49224878 G>A maps to NM_024603.2 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr10:13489308 C>T maps to ENST00000396900 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr19:12864106 C>T maps to NM_017682.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:70072611 A>G maps to NM_032735.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:45253306 C>T maps to NM_153274.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr20:17479637 G>A maps to NM_001195.3 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:102004719 G>A did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:78415118 A>T maps to NM_001713.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr5:78376592 C>T maps to NM_017614.4 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr12:32369194 C>G maps to NM_001714.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr12:32481321 C>A maps to NM_001714.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22481547 C>T maps to NM_018688.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:102195287 C>T maps to NM_182962.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MK-01A-11D-A364-08 chr17:76212095 C>T maps to NM_001012271.1 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:32728304 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:32756564 C>T maps to NM_016252.3 L4080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr15:91312418 C>G maps to NM_000057.2 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr15:91346838 G>A maps to NM_000057.2 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr10:22615873 T>A maps to NM_005180.6 C56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:22051964 C>T maps to NM_006129.4 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:69092996 G>A maps to NM_014482.1 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr23:50653912 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:6751118 G>T maps to NM_001200.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:79792151 C>T maps to NM_198892.1 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr14:54417157 G>A maps to NM_130850.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr6:55684507 C>A maps to NM_021073.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:55746113 C>T maps to NM_001719.2 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr2:203420160 A>T maps to NM_001204.6 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr2:203379699 G>T maps to NM_001204.6 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:43285946 G>A maps to NM_014753.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:43319070 C>T maps to NM_014753.3 R1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr23:15574249 C>T did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr15:83935779 C>T maps to NM_001717.3 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr9:16419334 G>A maps to NM_017637.5 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr1:151011473 G>A maps to NM_138278.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:112969474 C>T maps to ENST00000273395 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:13601500 G>A maps to NM_148894.2 S2341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr4:13601209 G>A maps to NM_148894.2 C2438C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr4:13606318 C>T maps to NM_148894.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:13604755 C>T maps to NM_148894.2 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:149871900 C>T maps to NM_016074.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:198640395 C>T maps to NM_197970.2 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr20:36952274 G>T maps to NM_001725.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:31619500 G>A maps to NM_174897.2 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr17:65907563 C>T maps to ENST00000321892 D1314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr17:65916198 C>T maps to ENST00000321892 R1959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:65942212 G>A maps to ENST00000321892 V2589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:41226393 C>T maps to ENST00000471181 G1565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:41244007 G>A maps to ENST00000471181 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr13:32911290 A>T maps to NM_000059.3 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:32914548 C>T maps to NM_000059.3 N2019N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr22:50217770 G>A maps to ENST00000342989 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50187715 G>A maps to ENST00000342989 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:15366906 C>T maps to NM_058243.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:137485405 G>A maps to NM_139199.1 G1067G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:37702214 C>T maps to NM_018310.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr17:59858253 G>A maps to NM_032043.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr5:34925037 A>G maps to NM_018321.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:36168827 C>T maps to NM_015695.2 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:135572581 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr23:79942410 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:79984394 C>A did not map to a codon.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr23:79945311 A>G did not map to a codon.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr3:49698532 C>A maps to NM_003458.3 G3085G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr3:49700780 C>T maps to NM_003458.3 S3730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49690939 C>T maps to NM_003458.3 L1317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr11:122848488 G>A maps to NM_001098169.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:93768863 G>A maps to NM_003972.2 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:93722416 C>T maps to NM_003972.2 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:93753480 G>T maps to NM_003972.2 G1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:13424826 T>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:3640680 G>A maps to NM_032444.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3639504 C>T maps to NM_032444.2 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr10:124050673 C>G maps to ENST00000368994 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr19:1986927 G>A maps to NM_017797.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr14:93709032 A>T maps to NM_001002860.2 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr14:93708855 G>A maps to NM_001002860.2 V1054V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr6:38548003 G>A maps to NM_052893.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr6:38545496 T>A did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr23:100630265 C>A did not map to a codon.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr6:26509215 C>T maps to NM_001732.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:26407899 A>T maps to NM_007048.5 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr6:26452500 C>T maps to NM_006994.4 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr6:26452086 G>C maps to NM_006994.4 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32363885 G>A maps to ENST00000468270 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32363945 A>G maps to ENST00000468270 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:180338567 G>A maps to NM_001040462.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:103221812 C>T maps to NM_033637.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:111398966 T>C maps to NM_004336.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr15:40501920 G>A maps to ENST00000412359 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:40462753 G>T maps to ENST00000412359 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:41900302 C>T maps to NM_004053.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr6:41889338 G>A maps to NM_004053.3 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:56381739 G>A maps to NM_004758.2 V1855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:56400900 C>T maps to NM_004758.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr10:63525767 C>G maps to NM_173554.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr10:121616906 C>T maps to NM_024834.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr10:121591576 G>A maps to NM_024834.2 N583N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:124457683 G>A maps to NM_001010912.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:96971775 T>C maps to NM_207321.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr10:127441483 G>C did not map to a codon.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr10:21805482 C>T maps to NM_207371.3 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr10:21804624 G>A maps to NM_207371.3 C709C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:21804813 C>T maps to NM_207371.3 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr10:5765642 G>T maps to NM_017782.4 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:72531146 C>T maps to NM_152710.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr10:99968461 A>G maps to ENST00000314594 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr10:82185668 C>T maps to NM_032333.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:50532617 G>A maps to NM_001135196.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr10:50532017 C>T maps to NM_001135196.1 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr10:50256601 G>A maps to NM_001031746.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr10:50315735 G>A maps to NM_001031746.3 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:103789493 G>A maps to NM_024541.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:103649192 G>A maps to NM_024541.2 H612H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:105923980 T>C maps to ENST00000389588 A1040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:105945829 G>A maps to ENST00000389588 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr10:115527187 C>T maps to NM_182601.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr10:115535574 T>G maps to NM_182601.1 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr10:128118365 G>A maps to NM_001004298.2 R651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr10:134261456 C>G maps to NM_173541.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:8942943 C>T maps to NM_020643.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr11:76257109 T>C maps to ENST00000393457 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr11:76237543 G>A maps to ENST00000393457 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:555840 C>T maps to NM_173573.2 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:33596409 C>T maps to ENST00000389726 Q1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr11:33581457 G>A did not map to a codon.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:122774731 G>A maps to NM_024806.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:101946633 G>T maps to NM_032930.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:101946620 C>T maps to NM_032930.2 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr11:86055701 C>T maps to NM_016401.3 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr11:63581247 G>A maps to NM_138471.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:109294694 C>T maps to NM_207645.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr11:111404528 C>A maps to NM_207430.2 S160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:61544761 C>T maps to NM_001127392.1 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr11:61533648 C>T maps to NM_001127392.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr12:53693738 T>C did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr12:82792602 C>A maps to NM_032230.2 Y187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr12:82796856 T>C maps to NM_032230.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:32135027 C>A maps to NM_018169.3 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:32135814 C>T maps to NM_018169.3 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:32134716 A>G maps to NM_018169.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:32138031 C>T maps to NM_018169.3 N1381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:32138301 C>T maps to NM_018169.3 N1471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:40085892 C>T maps to NM_001031748.2 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr12:103700091 C>T maps to NM_001099336.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:112616739 G>A maps to NM_001109662.2 S3614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:112622029 G>T maps to NM_001109662.2 P3408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:112622182 C>T maps to NM_001109662.2 A3357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:112622524 G>A maps to NM_001109662.2 G3243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:112672996 G>A maps to NM_001109662.2 S1761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:112711576 G>A maps to NM_001109662.2 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:97085089 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:97098575 T>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:97078468 G>A maps to ENST00000342887 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:97078926 G>A maps to ENST00000342887 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:97158976 G>A maps to ENST00000342887 S1179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr12:80647294 C>T maps to NM_173591.3 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:25148934 C>T maps to NM_001101339.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:25149159 C>T maps to NM_001101339.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr13:111973279 C>T maps to NM_152324.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:46937274 G>A maps to NM_025113.2 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr13:39587195 G>A maps to NM_025138.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr13:39586309 C>T maps to NM_025138.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr13:31531141 A>T maps to NM_152325.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr13:44464252 T>C maps to NM_153218.2 I379I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr13:31498490 A>T maps to NM_032849.3 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:57103317 T>C did not map to a codon.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr14:90755414 C>T maps to NM_017970.2 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:90767696 G>A maps to NM_017970.2 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:93653012 G>A maps to NM_001098621.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr14:81251837 G>A maps to NM_152446.3 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:91647608 T>C maps to NM_001102368.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:77297580 C>T maps to NM_194287.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr14:24769364 C>T maps to NM_174913.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:95903245 A>G maps to NM_152592.3 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:65031489 C>T maps to NM_172365.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr14:23467791 G>A maps to NM_021944.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr15:40675137 T>C maps to NM_033286.3 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr15:81427610 G>T maps to ENST00000458088 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:76430182 C>A maps to NM_152335.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr15:90447060 G>A maps to ENST00000398333 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:90451587 G>A maps to ENST00000398333 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:90137696 C>T maps to NM_152259.3 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr15:65871952 C>G maps to ENST00000420799 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:39544512 G>A maps to NM_207445.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:39544512 G>A maps to NM_207445.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:34649646 C>T maps to ENST00000438749 D1136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr15:34648410 C>A maps to ENST00000438749 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr15:44094001 T>G maps to NM_016400.3 *130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:613341 G>A maps to ENST00000293874 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr16:67700163 T>C maps to NM_032140.1 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr16:67699023 C>A maps to NM_032140.1 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr16:58036475 C>T maps to NM_024598.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr16:2512432 C>T maps to NM_025108.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:19693653 C>T maps to NM_020314.5 C912C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:8722914 C>T maps to NM_024109.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr16:67159902 C>T maps to NM_025187.3 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:9210615 G>A maps to NM_014117.2 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:2259562 G>A maps to NM_182563.3 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:58149202 G>C maps to NM_013242.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:46836914 G>A maps to NM_001001436.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:72949180 C>A maps to NM_030630.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:29231392 G>A maps to NM_024683.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr17:10614355 C>G maps to NM_020233.4 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr17:79207798 C>T maps to NM_144679.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:79207241 G>A maps to NM_144679.2 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr17:34192289 C>T maps to NM_152781.2 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr17:8138501 A>C maps to NM_025099.5 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79514340 G>A maps to NM_025161.5 N589N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7330458 T>G maps to NM_175734.4 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr17:71232289 G>T maps to NM_017941.4 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr17:7160287 G>A maps to NM_203414.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr17:3716469 C>T maps to NM_001114118.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74729656 C>T maps to ENST00000317409 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:36997588 G>A maps to NM_001080465.2 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:77798608 G>A maps to NM_024805.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:43796460 T>C maps to NM_145055.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr18:30517983 G>A maps to NM_001105528.1 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:30554608 G>A maps to NM_001105528.1 Q809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr18:30913135 A>T did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr18:21110077 C>T maps to NM_013326.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:1234614 C>T maps to ENST00000382477 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr19:1235782 G>A maps to ENST00000382477 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr19:3551145 G>A maps to NM_021731.2 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2278606 G>A maps to NM_198532.2 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:33464131 C>A maps to NM_152266.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:33465048 G>A maps to NM_152266.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr19:16614048 G>A maps to NM_032207.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:18679398 C>T maps to NM_024069.3 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44241780 G>A maps to NM_019108.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr1:22973819 G>A maps to NM_172369.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr1:22974074 C>T maps to NM_172369.3 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:77040181 G>A maps to ENST00000392445 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:24890278 C>T maps to NM_178540.3 D46D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-7330-01A-11D-2114-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:7254671 G>A maps to NM_016546.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:7177942 C>T maps to NM_001734.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:244724124 G>A maps to NM_001130957.1 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:111494602 C>T maps to NM_018372.3 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr1:200878354 C>T maps to NM_018265.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr1:200880922 G>A maps to NM_018265.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:162824959 G>A maps to NM_178550.4 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr1:36786087 G>A maps to NM_001162530.1 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:179452331 C>T maps to NM_144696.4 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:92709885 G>A maps to NM_001012425.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr1:75038905 C>A maps to NM_001002912.4 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr1:75038380 G>T maps to NM_001002912.4 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:75037028 C>T maps to NM_001002912.4 Q1455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:75037217 C>T maps to NM_001002912.4 E1392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:75102122 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:3807510 G>A maps to NM_207356.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:55168414 C>T maps to ENST00000454855 C1216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:55280636 C>T maps to NM_001110533.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:55277778 C>T maps to NM_001110533.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:154173059 G>A maps to NM_001010979.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr1:36181894 C>A maps to NM_152374.1 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:28209433 C>T maps to NM_001105556.1 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:154179946 T>A maps to NM_001098616.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr1:150255958 G>A maps to NM_144697.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr1:226182979 G>A maps to NM_152608.3 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:156702120 G>A maps to NM_015997.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr1:156704061 C>T maps to NM_015997.3 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:156263001 T>C did not map to a codon.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr1:60456395 C>A maps to NM_152377.2 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:16559012 G>T maps to NM_030907.3 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16559498 G>A maps to NM_030907.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr1:34684352 A>C maps to NM_001134734.1 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr6:31911053 C>T maps to ENST00000437789 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:31910872 C>T maps to ENST00000437789 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr20:55099932 T>G maps to NM_001012971.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:2796318 C>T maps to NM_080739.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr20:44515341 G>A maps to NM_080608.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31652620 C>T maps to NM_182658.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr20:31673923 C>T maps to NM_182519.2 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr20:31682955 C>A maps to NM_182519.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr20:31671326 C>A maps to NM_182519.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr20:20232250 T>C maps to ENST00000389655 N727N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:20071553 C>T maps to ENST00000389655 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:24959424 C>T maps to NM_020531.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr20:18794833 G>A maps to NM_178483.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr20:56726067 T>G maps to NM_178456.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr20:56735826 C>T maps to NM_178456.2 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr20:10603339 G>A maps to NM_001009608.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:45941816 C>T maps to ENST00000443468 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr21:33651139 G>T maps to NM_018944.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr21:33887451 C>T maps to NM_058187.3 N426N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr22:38340507 C>T maps to NM_032561.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr22:32794015 A>G maps to NM_014306.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:24982099 G>A maps to NM_207644.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr22:45595784 G>A maps to NM_001009880.1 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:118984806 C>T maps to NM_014807.3 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr2:27804460 C>A maps to NM_032266.3 S1674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr2:220038175 G>A maps to NM_015680.4 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:26671661 T>C maps to NM_145038.2 C500C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr2:10350626 G>A maps to NM_182626.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr2:88826008 G>A maps to NM_152670.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27360639 G>A maps to NM_178553.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:241831175 C>T maps to NM_001085437.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr2:241827876 G>A maps to NM_001085437.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr2:99413923 C>T maps to NM_207362.2 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr2:99448879 G>A maps to NM_207362.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr2:210993895 A>G maps to NM_152519.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:29295480 G>A maps to NM_001029883.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr2:29295351 C>T maps to NM_001029883.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr2:29296437 G>A maps to NM_001029883.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr2:120078760 G>A maps to NM_001017927.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:170502638 G>A maps to NM_001085447.1 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:24406451 T>A maps to NM_001040710.1 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr2:63660944 G>T maps to NM_015910.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr19:6697480 G>A maps to NM_000064.2 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:6693081 G>A maps to NM_000064.2 Y1081Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr19:6718309 G>A maps to NM_000064.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:112724715 T>C maps to NM_015412.3 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr3:112732170 C>A maps to NM_015412.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:14746119 C>T maps to NM_032137.4 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:44442727 G>T maps to NM_173826.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:44399286 G>C maps to NM_173826.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:133647491 C>T maps to NM_025041.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:43121555 G>T maps to NM_032806.4 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:196236506 C>T maps to NM_001077657.1 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:111821805 C>T maps to NM_001171747.1 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr3:49842263 G>A maps to NM_203370.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49842152 C>T maps to NM_203370.1 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr3:192517392 G>T maps to NM_178496.3 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:49313858 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:69047212 C>T maps to ENST00000383701 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:57843408 G>A maps to NM_032313.2 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr4:100434270 G>A maps to NM_032149.2 Q11Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr4:37591964 C>T maps to NM_018302.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr4:8467103 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr4:121961145 C>T maps to NM_024574.3 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr4:99030363 T>C maps to NM_174952.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr4:184614172 C>T maps to NM_021942.4 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr4:184595880 T>C maps to NM_021942.4 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr9:123805396 C>T maps to NM_001735.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr9:123725994 T>C maps to NM_001735.2 E1414E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr5:31534434 A>T maps to NM_018356.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:31551422 C>T maps to NM_018356.2 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:175722172 C>T maps to ENST00000443967 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr5:36225708 C>A maps to NM_001085411.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:37167159 G>A maps to NM_023073.3 D2463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:37176038 G>A maps to NM_023073.3 Q1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:37183046 G>A maps to NM_023073.3 L1746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr5:179264449 G>A maps to NM_016175.3 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr5:41160289 G>T maps to NM_001115131.1 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr5:41159223 G>A maps to NM_001115131.1 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr5:41172405 T>A maps to NM_001115131.1 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:11714745 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:11768592 C>T maps to NM_001143948.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:165715063 C>T maps to NM_144980.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr6:35754857 C>T maps to NM_001010886.3 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr6:47846329 G>A maps to NM_001013732.3 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr6:97616032 G>A maps to NM_198468.2 L975L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr6:127796911 G>A maps to NM_001012279.2 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:127797039 G>A maps to NM_001012279.2 Q711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr6:118790442 T>G maps to NM_001042475.2 T682T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr6:118790274 C>T maps to NM_001042475.2 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:36298374 C>T maps to NM_001010903.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:31731262 C>T maps to NM_001039651.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:31734101 G>A maps to NM_025258.2 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr6:170175419 G>T maps to NM_018341.1 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr6:36887409 C>T maps to NM_152734.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr5:40958241 T>C maps to NM_000587.2 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr7:31746866 C>T maps to NM_006658.4 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr7:86848786 G>A maps to NM_024315.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr7:39606041 T>C maps to NM_020192.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:39612283 A>G maps to NM_020192.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr7:66413639 C>T maps to NM_017994.4 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:1049776 G>A maps to NM_032350.5 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100086756 G>A maps to ENST00000423930 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr7:120768458 A>C maps to NM_024913.4 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:112579784 G>A maps to NM_152556.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:57372340 T>C maps to NM_000562.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139841130 C>T maps to NM_000606.2 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:96047720 C>T maps to NM_152416.2 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:39311237 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:39341246 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr9:35662634 C>T maps to NM_032818.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:35662652 A>G maps to NM_032818.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:130473654 C>T maps to NM_001012502.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr9:131038452 G>A maps to NM_001040011.1 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr9:35042437 C>T maps to NM_203299.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:34381367 G>A maps to NM_032596.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr9:97522700 T>A maps to NM_001193329.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:77563092 G>T maps to NM_017998.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:26842622 T>C maps to NM_024828.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr9:114468872 C>A maps to NM_173521.3 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:95869989 G>A maps to NM_032310.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:15744746 A>G maps to NM_173550.2 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:15778979 G>A maps to NM_173550.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr9:136260869 C>G maps to NM_153710.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr9:135698625 G>T maps to NM_152572.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr9:135702409 G>A maps to NM_152572.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr8:86249176 G>A maps to NM_001738.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:63632618 G>A maps to NM_001218.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr8:86163131 C>T maps to NM_198584.2 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr1:9019054 C>T maps to ENST00000413627 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr8:61137093 A>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:61178596 C>A maps to NM_004056.4 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:49956950 G>A maps to NM_001079670.1 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:227152756 G>A maps to NM_020247.4 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:227153069 C>T maps to NM_020247.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr22:24530348 C>G maps to NM_012295.3 L1571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr22:24460517 G>A maps to NM_012295.3 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:24562791 G>A maps to NM_012295.3 R1731R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr19:48533839 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr22:30125183 C>A maps to NM_182527.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr1:65142589 C>T maps to ENST00000371073 C996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:13325396 G>A maps to NM_023035.2 D1923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr19:13414686 G>A maps to NM_023035.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr9:140809211 G>A maps to ENST00000277549 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr12:2764405 T>G did not map to a codon.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr12:2676867 G>A maps to NM_199460.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr12:2566834 C>T maps to NM_199460.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr3:53531239 G>C maps to NM_001128840.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr3:53809969 C>T maps to NM_001128840.1 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:181725166 C>T maps to ENST00000357570 Y1355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:181727099 C>T maps to ENST00000357570 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:181708365 C>A maps to ENST00000357570 G1232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:181686337 C>T maps to ENST00000357570 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr1:181680188 C>T maps to ENST00000357570 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr1:181741294 C>T maps to ENST00000357570 N1689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr23:49069197 G>A did not map to a codon.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr23:49072960 T>G did not map to a codon.
Sequencing variant TCGA-M7-A722-01A-12D-A364-08 chr23:49081346 A>C did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:48703835 C>T maps to NM_018896.3 D2286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr17:48685231 G>A maps to NM_018896.3 S1519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr17:48678109 G>A maps to NM_018896.3 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr17:48650040 C>T maps to NM_018896.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48646293 G>A maps to NM_018896.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48680422 C>T maps to NM_018896.3 S1344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr22:40066134 C>T maps to NM_021096.3 V1429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr22:40055482 G>A maps to NM_021096.3 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr1:201046059 G>A maps to NM_000069.2 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr1:201046221 G>A maps to NM_000069.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr1:201046245 C>T maps to NM_000069.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:81667506 G>A maps to NM_000722.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:81626554 A>T maps to NM_000722.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:54930847 C>T maps to NM_018398.2 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:55038846 C>T maps to NM_018398.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr12:2022194 C>T maps to NM_172364.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:1993987 G>A maps to NM_172364.4 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:1995181 G>A maps to NM_172364.4 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr17:37341090 C>G maps to NM_000723.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr10:18429691 G>T maps to NM_201596.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:18439867 G>A maps to NM_201596.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr2:152732967 C>A maps to NM_000726.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr2:152698422 C>T maps to NM_000726.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr22:36960763 G>A maps to NM_006078.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr22:36960757 C>T maps to NM_006078.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr22:36960571 C>T maps to NM_006078.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:24373177 C>T maps to NM_006539.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:65026807 G>A maps to NM_014405.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:65021028 C>T maps to NM_014405.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr17:64880939 C>A maps to NM_014404.1 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr19:54444868 G>A maps to NM_031896.4 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:54483211 G>A maps to NM_031895.5 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr2:27455406 C>T maps to NM_004341.3 Q913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr2:27445188 A>G maps to NM_004341.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27447924 C>T maps to NM_004341.3 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27454972 T>C maps to NM_004341.3 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr11:115047193 C>A maps to NM_014333.3 *443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:115099881 G>A maps to NM_014333.3 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:115109304 G>A maps to NM_014333.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr1:159163348 C>T maps to NM_021189.3 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr1:159166232 C>T maps to NM_021189.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:159162425 C>T maps to NM_021189.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr3:62535599 C>G maps to ENST00000383709 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:62570915 A>G maps to ENST00000383709 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:62518601 G>A maps to ENST00000383709 D745D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:122078449 G>A maps to NM_001167940.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr7:122111517 C>G maps to NM_001167940.1 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:7373782 C>T maps to NM_001170692.1 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr16:71419499 C>T maps to NM_001740.4 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:71423689 C>T maps to NM_001740.4 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr7:93108737 G>A maps to NM_001164737.1 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr10:105218100 G>A maps to NM_001001412.3 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr10:12595223 C>T maps to NM_153498.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:209785549 C>A maps to NM_020439.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:209785231 G>A maps to NM_020439.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr5:149602667 G>A maps to NM_015981.3 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr7:44259780 G>A maps to NM_001220.4 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:114530359 G>A maps to ENST00000515496 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr5:110819728 G>A maps to NM_001744.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:121712245 G>A maps to NM_006549.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:138707775 C>T maps to ENST00000409386 A1460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:138714574 G>A maps to ENST00000409386 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:7723411 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr12:67700300 T>C maps to NM_018448.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr12:67700006 A>T maps to NM_018448.3 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FO-01A-21D-A364-08 chr3:12845100 C>T maps to NM_001162499.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:12869093 C>T maps to NM_001162499.1 Y1122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr17:76993227 C>T maps to NM_138793.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr2:30961159 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr2:30957342 C>T maps to ENST00000295055 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:223962540 C>A maps to NM_001748.4 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr15:42679976 C>T maps to NM_000070.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr15:42681284 C>T maps to NM_000070.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42681140 C>T maps to NM_000070.2 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr23:110494482 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr16:55601018 C>T maps to NM_032330.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:18891970 C>T maps to NM_033328.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr7:2962845 G>A maps to NM_032415.4 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:2978405 G>A maps to NM_032415.4 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr7:2953047 G>A maps to NM_032415.4 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78156558 C>T maps to NM_024110.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78169063 G>A maps to NM_024110.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:40853135 C>T maps to NM_032587.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139264856 G>A maps to NM_052813.4 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr11:67191325 C>T maps to NM_001166222.1 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:111357884 C>T maps to NM_024537.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:2239047 G>A maps to NM_020764.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr16:2233834 G>A maps to NM_020764.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:73498256 G>A maps to NM_020753.3 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:90577856 C>T maps to NM_012115.3 S1616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr3:121994723 G>A maps to NM_001178065.1 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:96011268 G>A maps to ENST00000508830 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:65793238 G>A maps to NM_053054.3 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:65793292 G>A maps to NM_053054.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr11:65789324 G>A maps to NM_053054.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr11:65792833 G>A maps to NM_053054.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr14:92139266 G>A maps to NM_024764.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:38858383 C>T maps to NM_021185.4 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MG-AAMC-01A-11D-A41K-08 chr19:38858383 C>T maps to NM_021185.4 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr7:116198998 G>T did not map to a codon.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr7:116140405 A>G maps to NM_001233.3 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88967910 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:105422837 T>C maps to NM_170662.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:105438944 G>A maps to NM_170662.3 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr18:70209170 G>A maps to NM_182511.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:77758429 C>T maps to NM_005189.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr17:77809098 C>T maps to NM_003655.2 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:77808243 G>A maps to NM_003655.2 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:77809044 C>T maps to NM_003655.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr17:77768835 C>T maps to NM_020649.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:14037353 C>T maps to NM_017721.4 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr4:15564983 G>A maps to NM_001080522.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:70545918 C>T maps to NM_018237.2 R893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr9:131600403 C>A maps to NM_004059.4 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr9:131597625 G>A maps to NM_004059.4 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr3:42906719 C>A maps to NM_001296.4 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:42906500 G>A maps to NM_001296.4 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:42906815 G>A maps to NM_001296.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr4:186380215 T>A maps to NM_152775.3 K509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr4:186392097 C>G did not map to a codon.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr19:48801472 C>T maps to NM_144577.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BO-01A-61D-A257-08 chr19:48807366 C>A maps to NM_144577.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:131096731 G>C maps to NM_032357.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:48924840 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:205600 G>A maps to NM_145265.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:31683137 G>A maps to NM_194300.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:13869944 C>T maps to NM_030818.2 D144D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr7:92901949 C>T maps to NM_017667.2 Q236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:92970797 G>A maps to NM_017667.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr16:57738846 C>T maps to NM_032269.5 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:57760784 C>T maps to NM_032269.5 Y672Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr2:179702243 C>A maps to NM_173648.3 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr17:16593776 C>T maps to NM_014695.1 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:16593938 C>T maps to NM_014695.1 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr7:76885703 G>T maps to NM_020879.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124857793 C>T maps to NM_025004.2 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49897811 C>T maps to NM_144688.4 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:77290767 T>C maps to NM_001042784.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:159860403 G>C maps to NM_012337.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:159856422 C>T maps to NM_012337.2 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:49099405 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:44457978 G>A maps to NM_152499.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr8:27605730 G>C maps to NM_018246.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43047171 G>T maps to NM_001080850.2 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43076729 C>T maps to NM_001080850.2 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr3:180359821 C>T maps to NM_181426.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr17:78022496 C>A maps to NM_017950.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78011942 G>A maps to NM_017950.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:94763728 T>C maps to NM_001042399.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr12:94763797 T>C maps to NM_001042399.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:63898326 G>A maps to NM_145036.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr3:128758619 T>C maps to NM_024768.2 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr3:48474342 C>T maps to NM_024661.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48473934 G>A maps to NM_024661.3 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:113184564 G>A maps to NM_144718.3 R408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:107096616 C>T maps to NM_032600.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr17:80121089 G>A maps to ENST00000445854 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr12:82746932 A>G maps to NM_014167.4 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:119942900 C>T maps to NM_178499.3 R226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr12:123286201 C>A maps to NM_201435.3 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:56650073 G>A maps to NM_001141947.1 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:93127644 G>A maps to NM_181645.3 Q354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:130897504 C>T maps to NM_207310.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:539870 T>C maps to NM_032358.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:775121 C>T maps to NM_001031737.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:46914606 C>T maps to NM_032040.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:46915401 G>A maps to NM_032040.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr3:112357580 G>T maps to ENST00000447230 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr3:112324431 C>T maps to ENST00000447230 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:112357078 G>A maps to ENST00000447230 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:86106420 A>C maps to NM_001156474.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr11:96117581 T>C maps to NM_024725.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:96117749 C>T maps to NM_024725.3 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr2:56420171 G>A maps to NM_001080433.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:60615457 C>T maps to NM_024098.3 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66359022 G>A maps to NM_018219.2 G488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr11:64109489 C>A maps to NM_032251.5 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr14:91787514 G>A maps to NM_001080414.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:47773662 G>A did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:26491053 G>A maps to NM_000730.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr17:34431360 G>A maps to NM_002984.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr17:34641447 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:45077976 C>T maps to NM_001029835.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr13:37014262 T>C maps to NM_003914.3 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:68470882 T>C maps to NM_031966.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr23:50054015 A>G did not map to a codon.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr16:2506606 C>T maps to NM_001761.2 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:162868106 T>A maps to NM_199246.1 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr5:159680552 G>A maps to NM_024565.5 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:159680777 G>A maps to NM_024565.5 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:1333665 G>A maps to NM_030937.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:55669189 G>A maps to ENST00000442196 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:38711170 G>A maps to NM_001838.3 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:39373860 C>T maps to NM_005201.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr3:39374259 G>A maps to NM_005201.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:45942585 C>T maps to NM_031200.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr3:45943239 G>C maps to NM_031200.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr12:69986784 T>C maps to NM_006431.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156279037 G>A maps to NM_005998.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr21:30439888 C>G maps to NM_006585.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr6:74440152 C>T maps to NM_133493.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:74516565 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140012543 G>A maps to NM_001174105.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:7653873 G>A maps to NM_004244.4 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:7635314 A>G maps to NM_004244.4 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr12:7531633 G>A maps to ENST00000416109 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr1:158226846 C>T maps to NM_001763.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr1:158299692 G>A maps to NM_001764.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr1:158300733 G>A maps to NM_001764.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr1:158262072 A>T maps to NM_001765.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr1:158261880 T>C maps to NM_001765.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr1:158151488 C>T maps to NM_001766.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr1:158151248 G>A maps to NM_001766.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr1:158152719 G>A maps to NM_001766.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr1:158325303 C>T maps to NM_030893.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr3:112546283 G>A maps to NM_001008784.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr3:112546089 T>C did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr2:71058206 G>A maps to NM_015717.3 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr19:35831814 A>G maps to NM_001771.3 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr19:35832258 C>T maps to NM_001771.3 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr11:66082755 C>T maps to NM_020404.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr11:66082815 G>A maps to NM_020404.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:204591690 G>T maps to NM_006139.2 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:47563636 A>G maps to NM_012120.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:208062819 G>A maps to NM_001025109.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:15835905 G>A maps to NM_001775.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr19:45911966 G>A maps to ENST00000423698 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr11:118223126 G>A maps to NM_000073.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr23:135730413 G>A did not map to a codon.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:207930435 C>A maps to NM_172359.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr1:160654875 G>A maps to NM_001778.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr1:157805810 C>A maps to NM_005894.2 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr1:157805767 A>T maps to NM_005894.2 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr1:157803021 G>A maps to NM_005894.2 H333H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr12:56120994 G>A maps to NM_001780.4 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr12:56121075 G>A maps to NM_001780.4 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr17:7484693 A>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:80274163 C>T maps to NM_006137.6 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:62007560 G>A maps to NM_001039933.1 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr11:44626915 C>T maps to NM_002231.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr3:121828208 A>T maps to NM_175862.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:121822506 C>T maps to NM_175862.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr13:115016140 G>A maps to NM_003903.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr1:43828700 G>A maps to NM_001255.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr5:54410069 C>T maps to NM_001170402.1 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:54439342 G>A maps to NM_001170402.1 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48200533 C>T maps to NM_001789.2 E492E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr17:45219652 C>T maps to NM_001114091.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:45235646 C>A maps to NM_001114091.1 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr1:227203872 T>G maps to ENST00000366766 R1589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr14:103416202 G>T maps to NM_006035.3 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:103410510 G>A maps to NM_006035.3 S1375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65088566 G>A maps to NM_006779.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:19502540 C>T maps to NM_001178010.1 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr22:19502367 C>T maps to NM_001178010.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:91978650 C>T maps to NM_001134420.1 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr8:25341515 A>C maps to ENST00000434814 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:25365067 C>T maps to ENST00000434814 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:6958353 C>T maps to NM_031299.4 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:68847379 C>T maps to NM_004360.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr5:24509760 C>G maps to NM_006727.3 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:64984907 G>A maps to NM_001797.2 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:21755849 G>A maps to NM_004061.3 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr16:83704516 G>C maps to ENST00000268613 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:83065741 C>T maps to ENST00000268613 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:89245891 G>A maps to NM_004933.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr16:66946576 G>A maps to NM_004062.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr16:66944232 G>A maps to NM_004062.2 H699H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95158180 G>A maps to NM_001144663.1 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr18:25565627 G>A maps to NM_001792.3 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr18:59166541 C>T maps to NM_031891.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr20:44869812 G>A maps to NM_021248.1 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr10:73491777 G>A maps to ENST00000398860 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr10:73553230 C>T maps to ENST00000398860 S2187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr10:73468897 C>T maps to ENST00000398860 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr10:73544679 C>T maps to ENST00000398860 N1850N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr10:73544679 C>T maps to ENST00000398860 N1850N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr10:73558936 C>A maps to ENST00000398860 S2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:73491777 G>A maps to ENST00000398860 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:73574911 G>A maps to ENST00000398860 T3319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr14:23522820 C>T maps to NM_022478.3 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:58562617 G>A maps to NM_177980.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:58564158 C>T maps to NM_177980.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr20:60419779 C>T maps to NM_001794.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr20:60498513 C>T maps to NM_001794.2 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:66431993 C>T maps to NM_001795.3 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:31323129 C>A maps to NM_004932.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:31267786 C>T maps to NM_004932.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:61851609 G>T maps to NM_001796.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr16:61689557 T>C maps to NM_001796.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr5:26906107 C>T maps to NM_016279.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:26881625 G>A maps to NM_016279.3 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:26881664 G>A maps to NM_016279.3 D650D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr10:85972117 C>T maps to NM_033100.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr5:176003116 C>T maps to NM_001171976.1 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176004551 G>A maps to NM_001171976.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176008534 C>T maps to NM_001171976.1 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr7:105641938 C>T maps to NM_152750.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:617464 C>T maps to NM_021924.4 A808A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:62544620 T>C did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr17:37627876 C>T maps to NM_016507.2 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr17:37618972 A>T maps to NM_016507.2 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr17:37619370 G>A did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr17:37676289 A>G maps to NM_016507.2 L1015L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr17:37646963 C>T maps to NM_016507.2 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr7:40085625 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:40102430 G>A maps to NM_003718.4 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:40133804 G>A maps to NM_003718.4 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:90356035 G>A maps to NM_012395.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:205498651 G>A maps to NM_212503.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:205495958 C>T maps to NM_212503.2 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr6:110944513 A>T maps to NM_015076.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr12:56365357 T>C maps to NM_001798.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr9:90585481 C>G did not map to a codon.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr7:150752139 G>T maps to NM_004935.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr7:150754242 G>C maps to NM_004935.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr7:150752433 C>T maps to NM_004935.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr2:219825270 C>T maps to NM_003936.3 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:123171435 C>A maps to NM_018249.4 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr9:123165314 C>T maps to NM_018249.4 T1692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:123210311 C>T maps to NM_018249.4 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr17:46048773 G>T did not map to a codon.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr17:46054118 G>A maps to NM_176096.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr5:68565119 G>A maps to NM_001799.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:18627657 C>A did not map to a codon.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr12:12870887 G>T maps to NM_004064.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr12:12871203 T>G maps to NM_004064.3 L144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:22006195 G>A maps to NM_004936.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:125864269 A>G maps to ENST00000392693 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr23:139866375 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:5159510 G>A maps to NM_003818.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:5169771 G>A maps to NM_003818.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr6:31084296 C>T maps to NM_001264.4 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:72667139 T>C did not map to a codon.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:43026109 C>T maps to NM_001712.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr19:45211202 C>T maps to ENST00000396750 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:45207439 C>T maps to ENST00000396750 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:42312920 G>A maps to NM_001815.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:42301581 G>A maps to NM_001815.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr19:42187836 G>A maps to NM_006890.3 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr20:48807617 G>A maps to NM_005194.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr14:23587879 G>A maps to NM_001805.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:33870418 C>T maps to NM_001806.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:37444156 G>A maps to NM_005760.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:37454883 G>A maps to NM_005760.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr22:18029033 C>A maps to ENST00000400579 R1332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:17600945 G>A maps to NM_031890.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr12:51737622 G>A maps to NM_001971.5 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:11207595 C>T maps to NM_006561.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr22:46835237 G>A maps to NM_014246.1 C1418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr22:46760119 C>T maps to NM_014246.1 P2936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:109801498 C>T maps to NM_001408.2 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:109794458 C>G maps to NM_001408.2 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:109805881 C>T maps to NM_001408.2 C1609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48697958 G>A maps to NM_001407.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48699530 G>A maps to NM_001407.2 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr4:104041394 C>T maps to NM_001813.2 V2413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:104068647 C>T maps to NM_001813.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr4:104065637 C>G maps to NM_001813.2 T1665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr4:104044026 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:214826194 C>T maps to NM_016343.3 R2729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr1:214811276 G>A maps to NM_016343.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr23:100364925 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:25480618 C>T maps to NM_018451.3 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr16:67865130 G>A maps to NM_025082.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr5:122700258 T>C maps to NM_153223.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr4:56886919 G>A maps to NM_025009.3 R1098R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:56890765 G>A maps to NM_025009.3 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr15:49059644 A>C maps to NM_001194998.1 Y678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr11:117241959 T>C maps to NM_014956.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr1:243362461 A>G maps to NM_014812.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:243328144 A>G maps to NM_014812.2 I1039I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:243354605 A>G maps to NM_014812.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr18:13056130 C>G maps to NM_032142.3 S1181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:13087062 C>T maps to NM_032142.3 G1888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:34091236 C>T maps to NM_007186.3 I1680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:179990053 C>T maps to NM_014810.4 Q1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:180044192 G>T maps to NM_014810.4 R1868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr5:648007 G>A maps to NM_018140.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr18:12699202 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:101474432 A>G maps to ENST00000327230 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr9:131196778 G>A maps to NM_016174.4 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr22:47095219 G>A maps to NM_022766.5 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr22:47085926 G>A maps to NM_022766.5 C501C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr16:55907857 G>A maps to NM_001143685.1 N55N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:55880482 C>A maps to NM_001143685.1 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:57003378 C>T maps to NM_000078.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:31917902 G>A maps to ENST00000437789 W997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr1:196711059 G>A maps to NM_000186.3 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:196658724 G>A maps to NM_000186.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr1:196928039 G>T maps to ENST00000367421 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:196759313 A>G maps to NM_021023.5 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:196971636 G>A maps to ENST00000367414 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr1:196963262 A>T maps to ENST00000367414 K186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:57730820 G>A maps to NM_032866.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:57809087 C>T maps to NM_032866.3 S838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:4433427 C>T maps to NM_005483.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr10:50835781 G>A maps to NM_020549.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:50857556 G>A maps to NM_020549.4 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DK-01A-11D-A377-08 chr3:126445988 C>A maps to ENST00000508789 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:98192173 C>T maps to NM_001270.2 Q1681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr5:98215341 G>A maps to NM_001270.2 Q1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr5:98216806 T>G maps to NM_001270.2 V1011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:98192224 C>T maps to NM_001270.2 W1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:98192374 A>G maps to NM_001270.2 D1614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:146765329 T>C maps to NM_004284.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr15:93545417 G>A maps to NM_001271.3 L1383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:93489283 G>A maps to NM_001271.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:93552391 G>A maps to NM_001271.3 R1477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:7806621 C>T maps to NM_001005271.2 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr17:7811745 G>T maps to NM_001005271.2 E1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:6686949 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:6194780 G>A maps to NM_015557.2 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:40102131 G>A maps to NM_032221.3 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:40126824 G>A maps to NM_032221.3 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr8:61655593 C>T maps to NM_017780.2 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr14:21871247 A>G maps to NM_001170629.1 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:21860704 T>A maps to NM_001170629.1 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:21861823 G>A maps to NM_001170629.1 R2044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr16:53190609 T>A maps to ENST00000219084 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr16:53190624 C>T maps to ENST00000219084 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:53337809 C>T maps to ENST00000219084 G1964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:53358593 A>G maps to ENST00000219084 V2827V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:133428222 C>T maps to NM_001161344.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:93399079 C>T maps to NM_001275.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr20:5904577 C>T maps to NM_001819.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:54915145 C>T maps to NM_012110.2 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:899383 G>T maps to NM_001142676.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:883188 G>A maps to NM_001142676.1 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr3:419626 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:403457 C>T maps to NM_006614.2 C461C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr23:85212901 T>C did not map to a codon.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr23:85213926 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:85155678 G>A did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr8:23114022 C>T maps to NM_152272.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:184099096 G>A maps to NM_003741.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr23:109963153 C>T did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:74421956 G>T maps to NM_015424.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:136700841 C>T maps to NM_001006628.1 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:240070780 G>A maps to NM_000740.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr1:240070780 G>A maps to NM_000740.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr15:34355862 C>T maps to NM_012125.3 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:175618297 G>A maps to NM_001039523.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:3688729 C>T maps to NM_020402.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:61982380 T>C did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:42611139 G>T maps to NM_004198.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr15:32460274 G>A maps to NM_001190455.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7351904 C>T maps to NM_000747.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7359975 C>T maps to NM_000747.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr1:154543703 C>T maps to NM_000748.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:154544123 G>A maps to NM_000748.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:45671747 C>T maps to NM_003654.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr7:2473203 G>A maps to NM_018641.3 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr7:2472600 C>T maps to NM_018641.3 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr3:126260910 C>T maps to NM_152889.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:126260940 G>A maps to NM_152889.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr3:142840956 C>G maps to NM_004267.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:142841088 G>A maps to NM_004267.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr10:73767310 C>T maps to NM_004273.4 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr10:73765714 G>T maps to NM_004273.4 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:73767544 C>T maps to NM_004273.4 C252C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:71571389 C>A maps to NM_001166395.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:75564024 G>A maps to NM_024533.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr16:75513510 G>A maps to NM_021615.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:101718647 G>A maps to NM_014918.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:129520760 A>G maps to NM_175856.4 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr10:101960456 T>C maps to NM_001278.3 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr15:78403581 G>A maps to NM_006383.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:42795295 G>A maps to NM_015125.3 A792A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr16:11000407 C>T maps to NM_000246.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr15:65502036 C>A maps to NM_003613.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:1271164 C>T maps to ENST00000413636 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr16:69194304 T>C maps to NM_032830.2 N497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:69170681 C>T maps to NM_032830.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr16:69177240 G>A maps to NM_032830.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120150459 G>T maps to ENST00000392521 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:120156516 G>A maps to ENST00000392521 S1330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr12:120214535 A>C maps to ENST00000392521 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr12:120166305 C>T did not map to a codon.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr2:113514461 A>G maps to NM_152515.3 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr11:46801809 A>C maps to ENST00000415402 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr11:46772925 T>C maps to ENST00000415402 L1764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:46818415 G>A maps to ENST00000415402 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr5:80548570 C>T maps to NM_001825.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:80548555 C>T maps to NM_001825.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:80550291 G>A maps to NM_001825.2 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr3:33557514 C>T maps to ENST00000359576 E1379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:86916414 C>T maps to NM_006536.5 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr1:86898057 A>G maps to NM_006536.5 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:87041172 C>T maps to ENST00000263723 Y614Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:87043585 C>T maps to ENST00000263723 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:87045160 G>A maps to ENST00000263723 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:143043270 C>A maps to NM_000083.2 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr7:143013472 C>A maps to NM_000083.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:143018814 A>G maps to NM_000083.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:184075850 G>T maps to NM_004366.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr23:10176201 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr23:49689924 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:11898393 C>T maps to ENST00000376496 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr1:11889327 C>T maps to ENST00000376496 C399C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1498403 C>T maps to ENST00000382745 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr1:16351303 G>A maps to NM_004070.3 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16376333 C>T maps to NM_000085.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16377009 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:190126205 T>C maps to NM_006580.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:137717904 C>T maps to NM_001002026.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr23:106171820 T>G did not map to a codon.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr19:51227211 T>G maps to NM_002975.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr12:10163421 C>T maps to NM_001129998.1 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr19:14710849 C>T maps to ENST00000417570 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:74444923 G>A maps to NM_001011880.2 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr16:78064470 C>T maps to NM_005752.3 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr12:8289394 C>T maps to NM_016184.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:71047616 C>T maps to NM_173535.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr2:71044098 G>A maps to NM_173535.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:141635652 T>C maps to NM_013252.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr4:141317053 A>G maps to NM_004362.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr23:154528412 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr23:154507270 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:157214773 G>A maps to NM_001195555.1 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr12:122825727 C>A maps to ENST00000302528 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:122803804 G>A maps to ENST00000302528 Q1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:155240636 C>T maps to ENST00000368361 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:74914553 C>T maps to NM_001130028.1 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:10515165 G>A maps to NM_052964.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr4:56304466 T>G maps to NM_004898.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:45490617 G>A maps to NM_001294.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:150644647 G>A maps to NM_052995.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:9795232 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:9811642 G>A maps to NM_001009566.1 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:36211632 C>T maps to NM_007096.3 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:57724939 C>T maps to NM_004859.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr17:57754536 G>T maps to NM_004859.3 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:19198012 T>C maps to NM_007098.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr22:19241487 C>T maps to NM_007098.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr6:123319140 G>A maps to NM_001010852.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:123319047 G>A maps to NM_001010852.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr13:100518572 C>A maps to NM_206808.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:10290658 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr16:81735395 G>A maps to NM_198390.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:66600559 C>T maps to NM_052999.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:79029069 A>G maps to NM_153610.3 K1494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:79026180 C>T maps to NM_153610.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr8:87951838 C>T maps to NM_173538.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:128890475 C>A did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr18:72223613 C>T maps to NM_032649.5 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:72179720 C>T maps to NM_018235.2 Y232Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr4:47938583 G>A maps to NM_001142564.1 R712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr4:47938767 G>C maps to NM_001142564.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr4:47938974 G>A maps to NM_001142564.1 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:150911711 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr11:6262660 G>A maps to NM_001037329.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr23:21450760 C>A did not map to a codon.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr19:11649777 C>T maps to NM_001299.4 Y12Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:101120670 G>A maps to NM_020348.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A723-01A-12D-A32B-08 chr10:104678761 C>T maps to NM_017649.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:97493558 C>T maps to NM_017623.4 D537D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:97427090 C>T maps to NM_020184.3 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr16:58633153 G>A maps to NM_016284.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:32800948 G>C did not map to a codon.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:70735907 G>T maps to NM_014515.5 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr19:54656630 G>A maps to NM_014516.3 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:135106937 A>C maps to NM_001190850.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:78647371 G>A maps to ENST00000512485 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr8:17089970 A>G maps to NM_013354.5 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr12:56705039 T>C maps to NM_014255.5 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99722480 C>T maps to NM_152755.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr6:88854285 C>T maps to NM_016083.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr1:246810984 A>G maps to NM_152609.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:40730406 G>A maps to NM_024877.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr12:41316216 C>A maps to NM_001843.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr12:41323721 C>A maps to NM_001843.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:41410695 A>G maps to NM_001843.2 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr1:205033528 C>T maps to NM_005076.3 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:74414809 G>A maps to NM_020872.1 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr3:74315727 G>A maps to NM_020872.1 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:2613234 C>A maps to NM_175607.1 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr3:2944669 C>T maps to NM_175607.1 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:2944669 C>T maps to NM_175607.1 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:3030067 C>T maps to NM_175607.1 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:3084088 C>T maps to NM_175607.1 R832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:3085291 C>T maps to NM_175607.1 P905P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:100221464 C>T maps to NM_014361.2 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr3:1394065 G>T maps to NM_014461.2 G475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr17:40843293 C>T maps to NM_003632.2 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:40849590 G>A maps to NM_003632.2 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr7:146829587 C>T maps to NM_014141.5 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:147092699 G>T did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr16:76573709 C>T maps to NM_033401.3 H1104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:125521375 C>T maps to NM_130773.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr2:125547650 G>A maps to NM_130773.2 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr2:125262059 G>T maps to NM_130773.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:125521311 T>C maps to NM_130773.2 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr2:125547509 A>G maps to NM_130773.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr17:7842863 G>T maps to NM_001037144.4 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr17:7852809 G>T maps to NM_001037144.4 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr17:7836489 G>T maps to NM_001037144.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7842985 C>A maps to NM_001037144.4 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr17:40717504 G>T maps to NM_001042532.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:165548757 C>T maps to ENST00000392717 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:140151430 C>T maps to NM_015456.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr17:71193479 G>T maps to NM_018714.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr13:46050412 A>G maps to NM_031431.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:40263921 T>C maps to ENST00000255468 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr16:23436136 C>A maps to NM_153603.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr16:23417459 A>G maps to NM_153603.3 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:23400345 G>A maps to NM_153603.3 I736I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:69369128 G>A maps to NM_032382.4 D236D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr1:103400615 A>T maps to NM_080629.2 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr1:103428307 G>A maps to NM_080629.2 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:103491097 C>T maps to NM_080629.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr1:103405947 G>A maps to NM_080629.2 Q1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr6:33132637 G>A maps to NM_080680.2 D1618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:33157147 G>A maps to NM_080680.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr6:33143389 C>T maps to NM_080680.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr6:75884865 G>A maps to ENST00000322507 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:75822985 G>A maps to ENST00000322507 G2628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:75893363 G>A maps to ENST00000322507 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr10:71634885 G>A maps to ENST00000356340 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr8:121237424 A>T maps to NM_021110.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr8:121293157 A>T did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr9:101748354 C>T maps to NM_001855.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:101778331 C>T maps to NM_001855.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr10:105798242 G>A maps to NM_000494.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr10:105801072 G>A maps to NM_000494.3 R879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr10:105832988 T>A maps to NM_000494.3 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OA-01A-11D-A41K-08 chr21:46888240 C>T maps to ENST00000359759 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:46888393 G>A maps to ENST00000359759 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr17:48270009 G>A maps to NM_000088.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:94037157 G>A did not map to a codon.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr7:94052352 C>T maps to NM_000089.3 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:94050331 T>C maps to NM_000089.3 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr6:56035876 T>C maps to NM_030820.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:139788237 G>A maps to NM_152888.1 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr8:139833396 G>A maps to NM_152888.1 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr8:139890293 G>A maps to NM_152888.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr8:139629180 G>A maps to NM_152888.1 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:86590962 G>T maps to NM_152890.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr1:86488274 C>A did not map to a codon.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr1:86306931 T>C maps to NM_152890.5 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:86203177 C>T maps to NM_152890.5 W1561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:109740458 T>C maps to ENST00000333642 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr4:109767342 G>A maps to ENST00000333642 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:110223176 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr9:116968049 A>G maps to NM_032888.2 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:116930356 C>T maps to NM_032888.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr9:117052372 A>G maps to NM_032888.2 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:116984537 C>T maps to NM_032888.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr9:116931619 G>A maps to NM_032888.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr7:7410436 C>T maps to NM_001037763.2 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:189874961 T>C maps to NM_000090.3 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr2:189875580 A>T maps to NM_000090.3 K1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:189859301 C>T maps to NM_000090.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr13:111130443 G>A maps to NM_001846.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111138134 G>A maps to NM_001846.2 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111156529 G>T maps to NM_001846.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr13:110960469 G>C maps to NM_001846.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr13:111117852 C>T maps to NM_001846.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:228155517 C>A maps to NM_000091.4 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr2:228118886 C>G maps to NM_000091.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr2:228172603 A>G maps to NM_000091.4 Q1477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:228134635 C>T maps to NM_000091.4 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:74676895 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr23:107938641 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:107849987 C>T did not map to a codon.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr23:107423789 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:107402840 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:107406168 G>T did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr9:137593106 C>T maps to NM_000093.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr2:189909927 G>A maps to NM_000393.3 R1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:189906340 G>A maps to NM_000393.3 R1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:189940163 C>A did not map to a codon.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:10096992 T>A maps to NM_015719.3 K784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr21:47423617 C>T maps to NM_001848.2 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr21:47532286 C>T maps to NM_001849.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr2:238243485 G>A maps to NM_004369.3 S3004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:238266525 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:130284216 C>T maps to NM_001102608.1 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:48624752 C>T maps to NM_000094.3 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:48626075 C>T maps to NM_000094.3 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr3:48628921 G>A maps to NM_000094.3 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48615752 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48617237 C>A maps to NM_000094.3 G1712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48629118 G>A maps to NM_000094.3 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr3:48629868 C>T maps to NM_000094.3 Q336Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:70948979 C>A maps to NM_001851.4 G697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:61471945 C>T maps to NM_001853.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:3691605 C>T maps to ENST00000418971 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:149470003 G>A maps to NM_016094.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31294521 C>T maps to NM_053041.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr19:18898324 C>G maps to NM_000095.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr11:14480107 G>A maps to NM_001144061.1 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:139088198 G>A maps to NM_004766.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L2-01A-31D-A41K-08 chr3:128990697 G>A maps to NM_016128.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:130297070 C>T maps to NM_012133.4 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr7:99686976 C>G maps to NM_006833.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr7:99688237 C>T maps to NM_006833.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr12:120966915 C>T maps to NM_032314.3 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr14:74426129 T>C maps to NM_182476.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr4:47788868 G>T maps to NM_006587.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:27943826 C>T maps to ENST00000345068 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:27943973 G>A maps to ENST00000345068 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr16:4408454 G>A maps to NM_024535.3 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:4407210 C>T maps to NM_024535.3 A881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:4414862 C>T maps to NM_024535.3 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:84600555 G>A maps to NM_021149.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:98264504 C>T maps to NM_001862.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr6:75950897 C>T maps to NM_001865.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr3:148896262 A>G maps to NM_000096.3 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:148924001 G>T maps to NM_000096.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr3:148903045 C>T maps to NM_000096.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr3:148916152 C>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr16:19547944 T>G maps to NM_014711.4 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:130021607 G>A maps to NM_001868.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:129919384 G>T maps to NM_001869.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OA-01A-11D-A41K-08 chr7:129962464 G>A maps to NM_016352.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr19:17057992 C>T maps to ENST00000443236 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr10:93902801 A>T maps to NM_014912.4 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr10:101802207 C>T maps to NM_001308.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr8:87549806 C>A maps to NM_003909.3 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:87570574 C>T maps to NM_003909.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:36767796 G>T maps to NM_020939.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr6:36767772 G>A maps to NM_020939.1 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:24545426 C>T maps to NM_006032.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:12798660 G>A maps to NM_018340.2 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr16:12875120 T>C maps to NM_018340.2 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr2:211454903 G>A maps to NM_001122633.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:211421555 A>G maps to NM_001122633.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:211541793 C>T maps to NM_001122633.1 V1452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr2:211542609 G>A did not map to a codon.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr2:211438053 A>T maps to NM_001122633.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145622731 G>A maps to NM_013291.2 C785C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr14:92608696 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:9595848 C>G maps to NM_016207.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr1:1248290 G>A maps to NM_017871.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr7:99051617 G>A maps to NM_006693.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr22:51008808 G>A maps to NM_152245.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr19:50214113 G>A maps to NM_152359.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr19:50214008 G>A maps to NM_152359.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr1:53679182 C>A maps to NM_000098.2 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr23:88009168 G>T did not map to a codon.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr20:2776681 G>A maps to NM_019609.4 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:2774859 C>T maps to NM_019609.4 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr10:125506293 G>A maps to NM_198148.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr10:125528230 G>A maps to NM_198148.2 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:125528098 C>T maps to NM_198148.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr1:207818583 G>T maps to NM_175710.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr16:1709960 G>A maps to NM_020825.3 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr9:131860405 G>A maps to NM_000755.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:131864768 G>A maps to NM_000755.3 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:197313414 A>G maps to NM_201253.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr7:137569738 A>G maps to ENST00000456390 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr7:28527794 T>C maps to NM_182898.2 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:3786755 A>G maps to NM_004380.2 H1485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:3778252 C>T maps to NM_004380.2 A2265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3779686 G>A maps to NM_004380.2 N1787N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3807827 T>C maps to NM_004380.2 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:35495959 C>T maps to ENST00000429130 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr5:76251512 C>T maps to NM_001882.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:43907567 C>T maps to NM_001145146.1 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:43907850 C>T maps to NM_001145146.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr2:36691751 C>T maps to NM_016441.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr6:43275383 G>C maps to ENST00000449267 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr4:1389213 C>T maps to NM_175918.3 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr6:49665571 C>T did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr16:84906611 C>T maps to NM_031476.3 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:1339931 C>T maps to NM_016823.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:1340399 C>T maps to NM_016823.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:18709694 G>A maps to NM_004750.4 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18709604 G>A maps to NM_004750.4 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:1317491 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr1:152383266 G>A maps to NM_016190.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:86991076 T>A maps to NM_001143935.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr1:159683404 G>A maps to NM_000567.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:99655148 G>A maps to NM_018058.4 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr10:99667830 C>A maps to NM_018058.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:99640009 G>A maps to NM_018058.4 C605C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:99696032 G>A maps to NM_018058.4 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr22:25627720 C>T maps to NM_000496.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:209010716 G>T maps to NM_005210.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr2:208993061 G>A maps to NM_020989.3 C130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:56667534 G>A maps to NM_004077.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:53567191 G>A maps to NM_015989.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr20:47692014 C>T maps to NM_001316.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:47706243 C>T maps to NM_001316.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:110466716 C>T maps to NM_000757.4 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:149460504 G>A maps to NM_005211.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr23:1407463 G>T did not map to a codon.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr23:1407765 A>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:37322028 G>A maps to ENST00000262825 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:38172079 A>G maps to NM_000759.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:61949662 G>A maps to NM_020991.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75091726 C>T maps to NM_004383.2 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr8:3889496 G>A maps to NM_033225.5 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:2910128 T>A maps to NM_033225.5 S2505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr8:3263666 C>T maps to NM_033225.5 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr8:2806883 C>A maps to NM_033225.5 G3447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr8:3855495 G>A maps to NM_033225.5 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr8:2832108 G>A maps to NM_033225.5 A2868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:3141831 G>A maps to NM_033225.5 H1329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr8:2820828 G>A maps to NM_033225.5 C3123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr8:2886874 C>T maps to NM_033225.5 T2607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:34102146 C>T maps to ENST00000373381 P1554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:33985437 G>A maps to ENST00000373381 G3530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:34037246 G>A maps to ENST00000373381 F2574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr8:113657356 A>T maps to NM_198123.1 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:113277664 C>T maps to NM_198123.1 W3221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr8:113317093 G>A maps to NM_198123.1 R2708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr8:113256713 G>A maps to NM_198123.1 T3437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr8:113812388 A>G did not map to a codon.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr8:113358323 A>G did not map to a codon.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr8:113697663 G>T maps to NM_198123.1 S818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:113323357 T>A maps to NM_198123.1 G2578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:113529317 G>A maps to NM_198123.1 T1567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr8:113331064 C>A did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr8:114449050 T>A maps to NM_198123.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:70798272 C>A did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr4:70823023 G>A maps to NM_001891.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr4:70823036 G>T maps to NM_001891.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr15:64464143 G>A maps to NM_022048.3 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr15:75982727 T>C maps to NM_001897.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr15:75985563 G>A maps to NM_001897.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75975361 C>T maps to NM_001897.4 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75980588 C>T maps to NM_001897.4 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75981311 G>A maps to NM_001897.4 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75981968 G>A maps to NM_001897.4 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr8:68087550 C>T maps to ENST00000389042 L1027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:68074056 G>A maps to ENST00000389042 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NK-01A-12D-A34U-08 chr3:39185626 C>T did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:201453912 A>G maps to NM_001193572.1 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr20:18142698 A>G maps to NM_020536.4 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr11:19213896 C>T maps to NM_003476.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:53457673 C>A maps to NM_015235.2 G546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr23:134948024 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr23:120008935 G>A did not map to a codon.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr23:120007805 C>A did not map to a codon.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr23:120009179 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:120009361 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr23:153881612 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:19996933 C>A maps to NM_172241.2 G281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr14:39769117 A>G maps to ENST00000396158 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr6:132032075 C>A maps to NM_001145659.1 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr10:126682485 T>C maps to NM_022802.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr10:126682485 T>C maps to NM_022802.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr1:85029047 G>A maps to NM_004388.2 D283D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:56099192 C>T maps to ENST00000423479 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:56099036 G>A maps to ENST00000423479 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr20:56099165 T>C maps to ENST00000423479 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:38012926 C>T maps to NM_001008392.1 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:38022318 C>T maps to NM_001008392.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:138269726 C>T maps to ENST00000355078 H913H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr10:67680275 G>A maps to NM_013266.2 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:68940083 G>A maps to NM_013266.2 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:68940101 C>T maps to NM_013266.2 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:111754917 T>C maps to NM_003798.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:111761527 C>T maps to NM_003798.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr9:111734981 G>C maps to NM_003798.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr9:111746716 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr1:9931302 G>A maps to ENST00000361853 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr1:41475252 C>G maps to NM_001905.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr23:16720990 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr23:16707689 C>A did not map to a codon.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:10800224 G>C did not map to a codon.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:1780797 G>A maps to NM_001909.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:1780294 G>A maps to NM_001909.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr14:25043657 C>A maps to NM_001911.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr14:25043994 G>A maps to NM_001911.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr4:156860532 C>T maps to NM_001334.2 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:57576622 G>A maps to NM_001336.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr10:17032434 C>T maps to NM_001081.3 E1416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr10:16882352 G>C maps to NM_001081.3 Y3336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:16932469 G>A maps to NM_001081.3 N2885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr10:17089576 A>G maps to NM_001081.3 D1055D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr13:113909104 G>A maps to NM_001008895.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:113897424 C>A maps to NM_001008895.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr13:113899532 C>T maps to NM_001008895.1 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:119694002 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:107968472 C>T maps to NM_003478.3 F672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:43017805 G>A maps to NM_001168370.1 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:43172185 G>A maps to ENST00000354495 A1416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr6:33384485 G>A maps to NM_001014433.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr10:101503042 T>A maps to NM_015960.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:101845117 C>T maps to ENST00000360264 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:111652017 C>T maps to NM_015267.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr10:101993057 T>A maps to NM_018294.4 K515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:107309879 C>T maps to NM_152434.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:48994015 T>C maps to NM_025087.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:18924179 G>A maps to NM_001338.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr21:18924260 G>T maps to NM_001338.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr4:74735479 C>T maps to NM_001511.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:76943935 G>A maps to NM_001565.2 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118765270 C>T maps to NM_001716.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr2:237489878 C>T maps to NM_020311.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:237489378 C>T maps to NM_020311.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr5:139060932 C>A maps to NM_016463.7 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:139060173 C>T maps to NM_016463.7 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr23:144909434 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:35984804 G>A did not map to a codon.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr23:19984248 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr23:40506742 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:118676490 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr23:118678352 G>A did not map to a codon.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr23:105881005 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr23:23934358 T>C did not map to a codon.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr23:23956756 G>C did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:36103578 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:115593952 C>T did not map to a codon.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr11:61118522 G>A maps to NM_001161454.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr23:37660565 T>A did not map to a codon.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:37641373 G>C did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:145150821 G>A maps to NM_001916.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr15:22945110 G>A maps to NM_014608.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr15:22933657 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:22990103 C>T maps to NM_014608.2 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:22990196 C>T maps to NM_014608.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:156746768 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:156816381 C>T maps to ENST00000442283 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr23:83129064 C>T did not map to a codon.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:143995678 C>T did not map to a codon.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr15:75013054 A>T maps to NM_000499.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:75047380 C>T maps to NM_000761.3 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr6:31975462 T>C maps to NM_000500.5 *316Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:52779273 C>T maps to NM_000782.4 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:52779276 G>T maps to NM_000782.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:72359682 G>A maps to NM_019885.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr2:219677082 G>A maps to NM_000784.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr2:127958779 G>T maps to NM_001001665.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:127956951 C>T maps to NM_001001665.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr10:96827285 C>A maps to NM_000770.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr22:42525128 G>T maps to NM_000106.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr19:41626274 C>T maps to NM_000774.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:41700462 C>T maps to ENST00000301173 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr7:1024634 G>A maps to NM_017781.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:16040399 C>A maps to NM_021187.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr19:16040303 G>A maps to NM_021187.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr19:16006352 G>A maps to NM_001082.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr19:15662135 G>T maps to NM_173483.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:15662224 A>T maps to NM_173483.3 I513I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:15756623 C>A maps to NM_000896.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr19:15763395 G>A maps to NM_000896.2 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:15760046 C>T maps to NM_000896.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:15739225 C>T maps to NM_007253.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:187130277 C>T maps to ENST00000511608 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr4:187131662 G>T maps to NM_207352.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:47571859 C>T maps to NM_178134.2 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr8:59412636 A>T maps to NM_000780.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr23:77529209 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr23:77528835 T>G did not map to a codon.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr13:49281495 C>T maps to NM_020377.2 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:158283925 C>T maps to NM_004288.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:5018574 C>T maps to NM_018659.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:24807597 C>T maps to NM_015330.2 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr22:24717685 G>A maps to NM_015330.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:24726234 G>A maps to NM_015330.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr17:20109179 A>G maps to NM_001033553.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr21:27840879 G>T maps to ENST00000435845 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr21:27840930 G>A maps to ENST00000435845 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr14:59797407 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr6:39828786 G>A maps to ENST00000398904 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr6:39869130 C>T maps to ENST00000398904 D955D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:124535155 C>T maps to ENST00000408936 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:124521262 G>A maps to ENST00000408936 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr23:86068205 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr23:85769328 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:85769337 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:6474467 G>A maps to NM_139179.3 C201C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:61110227 C>A maps to NM_015533.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:61111397 G>A maps to NM_015533.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:109290786 C>T maps to NM_001917.4 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr12:109288094 G>A maps to NM_001917.4 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr9:90252884 C>T maps to NM_004938.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr9:90296531 A>T maps to NM_004938.2 K739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr15:64275808 C>T maps to NM_014326.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr19:3964646 G>T maps to NM_001348.1 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:3964790 C>T maps to NM_001348.1 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:159176047 G>A maps to NM_001122951.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:1418347 G>A maps to NM_018959.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr9:121930372 G>A maps to NM_014618.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:121930402 G>A maps to NM_014618.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr17:42828593 C>T maps to NM_145663.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:136501720 C>T maps to NM_000787.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:90072795 G>A maps to ENST00000392973 Q262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr11:20178065 G>A maps to ENST00000227256 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr9:37801315 C>G maps to NM_024345.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:24588973 C>T maps to NM_025230.4 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr23:125685747 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr23:125685211 G>A did not map to a codon.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr23:125685919 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr23:125685924 C>G did not map to a codon.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr23:125685733 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:125685776 C>T did not map to a codon.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr23:125298897 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr23:125299263 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:104433217 C>T maps to NM_015420.6 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:14070277 G>A maps to NM_138353.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr14:73418523 C>T maps to NM_015604.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:41984636 G>A maps to NM_001029955.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:69558432 T>C maps to NM_003861.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr1:167973819 T>C maps to ENST00000367840 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr1:167962659 G>A maps to ENST00000367840 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr23:27997689 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr23:27997699 T>C did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr23:27766320 C>A did not map to a codon.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr3:98519474 A>C maps to ENST00000326857 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:50994312 G>A maps to NM_005215.3 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:55038966 G>A maps to NM_053283.2 S93S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-J9-A52C-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr1:32674909 G>A maps to NM_001099434.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:6650984 C>T maps to NM_003737.2 Q1651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:6646560 G>A maps to NM_003737.2 D2338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr4:155254245 G>A maps to NM_017639.3 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr4:155256173 C>G maps to NM_017639.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr4:155242137 C>T maps to NM_017639.3 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr4:155253864 G>A maps to NM_017639.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr4:155298458 G>T maps to NM_017639.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:155157214 G>T maps to NM_017639.3 S2408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:155254287 G>A maps to NM_017639.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr4:155219105 C>T maps to NM_017639.3 R1665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr16:2293365 G>A maps to NM_001919.3 Y172Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:2290113 G>A maps to NM_001919.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr13:36402389 G>T maps to NM_004734.4 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:36700136 C>T maps to NM_004734.4 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:36778887 G>A maps to NM_033403.1 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:14961815 G>A maps to NM_001033855.1 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:53338245 G>A maps to ENST00000480258 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:112327914 T>C maps to NM_152624.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr13:95121165 G>A maps to NM_001129889.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr5:150095124 A>G did not map to a codon.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr17:79993877 C>T maps to NM_016286.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr7:50607642 G>A maps to NM_000790.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:53539388 G>A maps to NM_001160148.1 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:74034534 G>A maps to NM_019058.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:49391284 C>T maps to NM_015086.1 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:20982021 C>T maps to NM_005216.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr6:30865882 C>T maps to NM_013994.2 I756I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:30856710 C>T maps to NM_013994.2 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:162749927 T>C maps to NM_006182.2 C820C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:15747404 G>A maps to NM_004939.1 Q308Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:15770166 G>A maps to NM_004939.1 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:31236824 C>T maps to NM_030653.3 R75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr22:38881960 A>G maps to NM_001098504.1 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:118582238 C>T maps to NM_006773.3 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr23:134709031 G>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:47845306 C>T maps to NM_017895.7 R285R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KK-A8IM-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:135517390 C>A maps to NM_022779.7 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr23:41196664 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:41205565 C>T did not map to a codon.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr24:15023761 A>G did not map to a codon.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr24:15028969 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr24:15028885 A>C did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr24:15023866 G>T did not map to a codon.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr5:55094307 G>A maps to NM_024415.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr5:134152275 T>C maps to ENST00000452510 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:62496409 G>A maps to NM_004396.3 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr23:23018290 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr12:113612880 G>A maps to NM_001111322.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr7:44611158 T>C maps to NM_019082.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr9:32457377 T>C maps to NM_014314.3 E840E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr4:169227601 T>C maps to NM_017631.5 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:169195114 G>A maps to NM_017631.5 D808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:169209424 A>T maps to NM_017631.5 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:169227856 C>T maps to NM_017631.5 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:686973 G>A maps to NM_021008.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr6:35277529 C>T maps to NM_022047.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr16:90027429 G>C maps to NM_207514.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr16:90028533 G>A did not map to a codon.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr6:49986787 T>G maps to NM_001037497.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr20:210385 G>T maps to NM_080831.3 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr7:140285505 C>T maps to NM_015689.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:140301969 C>T maps to NM_015689.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:111737240 G>A maps to NM_024901.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr8:142178472 G>A maps to NM_014957.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:153913418 C>T maps to NM_014856.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:19358035 C>T maps to NM_017925.4 R1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:31545312 G>A maps to NM_144973.3 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:68947727 C>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:32200865 C>T maps to NM_001136029.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:32234676 C>T maps to NM_001136029.1 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:121015348 C>T maps to NM_022783.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr2:220285374 G>T maps to NM_001927.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr15:89074915 G>A maps to NM_017996.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:24742389 G>A maps to NM_001127453.1 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:117188501 C>T maps to NM_015404.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr22:19055730 G>A maps to NM_005137.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr22:20082237 C>T maps to NM_022720.6 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr12:56335368 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr12:56334138 G>A maps to NM_201554.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:234371287 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:234356981 G>T maps to NM_152879.2 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr17:54940142 G>A maps to NM_003647.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S0-01A-11D-A41K-08 chr3:185997729 G>A maps to NM_001346.2 Y234Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr13:42742921 A>G maps to NM_178009.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:42761256 C>T maps to NM_178009.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr7:137082143 A>T maps to NM_004717.2 L987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr7:137092657 G>A maps to NM_004717.2 T969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OF-01A-11D-A41K-08 chr23:50119073 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:50213385 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:46401087 C>T maps to NM_001105540.1 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr11:46397442 C>T maps to NM_001105540.1 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:74154093 C>T maps to NM_080916.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:55349365 G>A maps to NM_014762.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:71153384 C>A maps to NM_001360.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:71146657 C>T maps to NM_001360.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:79933788 T>C maps to NM_000791.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr12:49485160 C>T maps to NM_021044.2 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr16:72057374 C>T maps to NM_001361.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr19:12790631 C>A maps to NM_001930.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:24459435 C>T maps to NM_198083.3 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:24470244 C>T maps to NM_198083.3 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr23:2139236 C>T did not map to a codon.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr23:2184931 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:2161197 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:2161251 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:2184849 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:12131157 C>T maps to NM_018706.5 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr10:12129646 C>T maps to NM_018706.5 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr10:12149962 C>T maps to NM_018706.5 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:12139742 G>A maps to NM_018706.5 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:24544562 C>T maps to NM_001358.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:30627569 C>T maps to NM_003587.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:127525311 C>A maps to NM_018180.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:37662959 G>A maps to NM_021931.3 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:154010464 G>A maps to NM_020865.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:125449046 G>A maps to NM_032656.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr16:72130067 C>T maps to NM_014003.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:39050310 G>A maps to NM_198963.1 R1039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:95571439 G>A maps to NM_177438.2 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:95571526 T>C maps to NM_177438.2 K1050K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr20:61525226 G>A maps to NM_033081.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr20:61525241 G>A maps to NM_033081.2 T959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:61511163 G>A maps to NM_033081.2 S2048S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:61527731 G>A maps to NM_033081.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr20:61512747 C>T maps to NM_033081.2 L1520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr1:54360026 G>A maps to NM_000792.5 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr14:102027946 C>T maps to NM_001362.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr21:47961678 C>T maps to ENST00000318711 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:47959820 C>T maps to ENST00000318711 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr21:47987297 G>A maps to ENST00000318711 W1494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr12:51089054 A>T maps to NM_173602.2 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr12:51138472 G>T maps to NM_173602.2 E1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:51064978 G>A maps to NM_173602.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr10:408504 G>A maps to NM_014974.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr10:373035 C>T maps to NM_014974.2 S1278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr2:189599334 A>G maps to NM_052952.2 *105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr15:66618501 C>T maps to NM_001143688.1 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:233001354 G>A maps to NM_152383.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:231830154 T>C maps to NM_001164537.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr1:232144701 C>T maps to NM_001164537.1 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:223163993 G>A maps to NM_032890.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr23:153994550 G>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65547171 C>T maps to NM_138368.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr10:54076404 C>A maps to NM_012242.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:12029973 G>A maps to ENST00000450094 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49869054 C>T maps to NM_014419.3 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr8:12952651 C>T maps to NM_182643.2 P1090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:12950182 G>A maps to NM_182643.2 A1226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:12957580 C>T maps to NM_182643.2 T755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr8:12957109 G>A maps to NM_182643.2 H912H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:38135138 T>C maps to NM_007335.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr3:38139332 G>A maps to NM_007335.2 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr3:38155876 G>A maps to NM_007335.2 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:38104199 T>C maps to NM_007335.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr11:83195217 G>A maps to NM_001142699.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:83243768 T>C maps to NM_001142699.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr11:84245657 T>C maps to NM_001142699.1 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr17:7096377 C>T maps to NM_001365.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr17:7096280 G>A maps to NM_001365.3 R660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr10:79571785 C>T maps to NM_004747.3 T1406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr10:79571812 G>A maps to NM_004747.3 F1397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:1616603 C>T maps to ENST00000357934 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:1497833 G>A maps to ENST00000357934 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:35060647 C>T maps to ENST00000339266 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:170594701 G>A maps to NM_005618.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr14:75367845 G>A maps to NM_001933.4 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:75368921 C>T maps to NM_001933.4 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr10:124376759 T>G maps to ENST00000368915 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:124390528 G>A maps to ENST00000368915 G2026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr23:32380925 T>C did not map to a codon.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr23:31676188 G>A did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr23:32536159 C>T did not map to a codon.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr23:31986567 C>G did not map to a codon.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr23:31838131 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:32662408 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:78329224 G>A maps to NM_013391.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:36001088 G>A maps to NM_033317.4 P328P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KK-A7AW-01A-11D-A32B-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:50885065 C>T maps to NM_032110.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:118533573 C>A maps to NM_005509.4 T2556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:118487709 C>T maps to NM_005509.4 R1561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr5:118525451 G>A maps to NM_005509.4 P2395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr15:51750825 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr15:51855613 C>T maps to NM_001174116.1 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51795001 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:51795012 C>T maps to NM_001174116.1 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr10:70231684 G>A maps to NM_001080449.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr10:70196775 T>C maps to NM_001080449.1 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:52402840 G>A maps to ENST00000273600 P1950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr3:52412684 C>A maps to ENST00000273600 T2422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr3:52383436 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52391664 C>T maps to ENST00000273600 D1298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52426961 C>T maps to ENST00000273600 N3529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:124395092 G>A maps to NM_207437.3 K3218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:124416489 C>A maps to NM_207437.3 A4259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr3:57488128 C>T maps to NM_178504.4 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr17:76471407 G>A maps to ENST00000389840 D2807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr17:76510933 C>T maps to ENST00000389840 T1341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr17:76472713 G>A maps to ENST00000389840 D2684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr17:76566364 G>T maps to ENST00000389840 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr17:76496389 G>T maps to ENST00000389840 Y1865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr17:76482395 G>A maps to ENST00000389840 T2323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:76422600 G>A maps to ENST00000389840 A4307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:76488766 G>T maps to ENST00000389840 T2149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr17:76435216 G>A maps to ENST00000389840 N3906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:7673933 G>A maps to NM_020877.2 K1386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr17:7734508 C>T maps to NM_020877.2 G4112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:7680785 C>G maps to NM_020877.2 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:7682661 C>T maps to NM_020877.2 A1881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr17:7680921 G>A maps to NM_020877.2 W1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7644156 G>A maps to NM_020877.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7734418 G>A maps to NM_020877.2 E4082E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr16:20975443 C>T maps to NM_017539.1 L3254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr16:20952768 C>A maps to NM_017539.1 E3870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr16:21109951 C>T maps to NM_017539.1 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:21156619 G>A maps to NM_017539.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:13735946 T>C maps to NM_001369.2 L3850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:13824305 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr2:196673405 C>T maps to NM_018897.2 L3361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:196729520 G>A maps to NM_018897.2 I2286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:196765101 C>T maps to NM_018897.2 T1484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:196799425 G>A maps to NM_018897.2 S1120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:38820471 G>A maps to ENST00000327475 P1811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr6:38877388 G>T maps to ENST00000327475 L3191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr17:11687705 C>T maps to NM_001372.3 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:11656222 C>T maps to NM_001372.3 G2228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:11757588 C>T maps to NM_001372.3 S3259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:34517404 C>T maps to NM_012144.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr9:34490061 C>T maps to NM_012144.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:72306163 C>T maps to NM_023036.4 D452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:33036610 C>T maps to NM_001539.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr15:78558596 C>T maps to NM_001130183.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:186299281 C>T maps to NM_016306.4 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr9:34997171 C>T maps to NM_001135005.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr9:34993217 T>C maps to NM_001135005.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr3:128181920 C>G maps to NM_153330.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr3:132165394 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:180704807 G>T maps to NM_145261.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr7:102953048 T>C maps to NM_014377.1 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:96443193 C>T maps to NM_006260.4 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3707286 C>T maps to NM_005223.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr23:153631328 G>A did not map to a codon.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr11:6593108 A>T maps to NM_144666.2 K4719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:6519837 C>A maps to NM_144666.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr12:32884345 G>A maps to ENST00000381000 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:32886740 G>A maps to ENST00000381000 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:101636946 G>A maps to ENST00000342239 Y1589Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:101636967 C>T maps to ENST00000342239 E1582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:101639888 C>T maps to ENST00000342239 P1433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:10291512 C>A maps to NM_001130823.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:25467185 C>T maps to NM_175629.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:25469137 C>T maps to NM_175629.1 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:25505421 G>A maps to NM_175629.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:25468928 C>T maps to NM_175629.1 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31374387 C>T maps to NM_006892.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:44433837 C>T maps to NM_052951.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:129202689 G>A maps to ENST00000398025 L1418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:129231686 C>T maps to ENST00000398025 S1730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:225670000 G>A maps to NM_014689.2 R1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr2:225684222 T>G maps to NM_014689.2 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr2:225662682 G>A maps to NM_014689.2 Q1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:225796265 T>C maps to NM_014689.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr23:117700565 G>T did not map to a codon.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr23:117742297 A>G did not map to a codon.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr23:117775255 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:117788702 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr23:117805040 G>A did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:169507216 G>A maps to NM_004946.2 A1739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:169129424 G>A maps to NM_004946.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51101985 G>A maps to NM_004947.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51102012 G>A maps to NM_004947.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr3:50879109 G>A maps to NM_004947.4 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:51347718 C>T maps to NM_004947.4 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr7:111503617 A>T maps to ENST00000428084 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:111400345 G>A maps to ENST00000428084 Y1351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:111617287 G>A maps to ENST00000428084 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:25216577 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr8:25246689 G>A maps to NM_024940.6 A1405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:11325273 G>A maps to ENST00000319867 T1386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:63048922 T>C maps to ENST00000371140 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr9:428368 C>A maps to NM_203447.3 S1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr9:396792 C>T maps to NM_203447.3 S993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:3494034 G>A maps to NM_001145165.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr8:21768189 C>T maps to NM_003974.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176931271 C>G maps to NM_024872.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr6:83850060 C>A maps to NM_015018.2 S1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr6:83855350 C>T maps to NM_015018.2 Q1884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:83829479 C>T maps to NM_015018.2 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr21:37617883 C>T maps to NM_005128.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr21:37605186 G>C maps to NM_005128.2 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:2222179 C>T maps to ENST00000221482 H1004H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2214516 G>A maps to ENST00000221482 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65107960 C>T maps to NM_006268.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:101487276 T>C maps to NM_015958.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:101456140 G>A maps to NM_015958.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:49552741 G>A maps to ENST00000449701 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr2:116066819 G>T maps to NM_020868.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr2:116066820 G>T maps to NM_020868.3 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:66259192 C>T maps to NM_005700.3 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66259053 C>T maps to NM_005700.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr7:154667654 C>T maps to NM_130797.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:154143321 G>A maps to NM_130797.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr15:65790301 G>A maps to NM_197960.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:65759486 G>A maps to NM_197960.2 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr19:4694805 T>C maps to ENST00000357909 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr3:109031398 G>A maps to NM_138815.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr3:109050825 C>T maps to NM_018189.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:168698283 C>T maps to NM_001937.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:63976242 T>C maps to NM_173812.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:97544633 A>G maps to NM_000110.3 C992C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr10:134017270 G>A maps to NM_006426.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr2:27147849 G>A maps to NM_020134.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27121447 C>T maps to NM_020134.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr2:74750441 G>T maps to NM_133637.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:74750267 C>T maps to NM_133637.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr4:9783991 C>T maps to NM_000798.4 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr4:9783961 G>T maps to NM_000798.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr23:100513327 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr23:100511154 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:28654829 G>A maps to ENST00000438199 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr21:41684281 C>T maps to NM_001389.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr21:41551003 G>A maps to NM_001389.3 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr21:41719855 G>T maps to NM_001389.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr21:41385013 G>T maps to NM_001389.3 R1996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr11:117332279 G>A maps to NM_020693.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:117374665 C>T maps to NM_020693.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr8:120859293 T>C maps to NM_024094.2 Q171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr8:120865379 T>C maps to NM_024094.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:65178557 C>G maps to NM_032160.2 V1106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr18:29046691 C>T maps to NM_001944.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr18:28986326 C>T maps to NM_001134453.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr18:28992795 G>A maps to NM_001134453.1 A806A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr20:35383220 C>T maps to NM_001145315.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr6:7580295 G>A maps to NM_004415.2 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:56341000 T>C maps to ENST00000361203 K7059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr6:56373516 C>T maps to ENST00000361203 W6139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:56485249 C>T maps to ENST00000281662 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:56417269 G>A maps to ENST00000361203 D5229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr6:56341012 A>T maps to ENST00000361203 T7055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr20:17581393 G>T maps to NM_006870.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:205132934 G>A maps to NM_015375.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:18724892 G>A maps to NM_080820.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:212274087 T>C maps to NM_016448.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:25611101 G>A maps to NM_021907.3 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr7:76112080 A>G maps to NM_020892.2 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr12:58002361 G>A maps to NM_178502.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:242625236 G>A maps to NM_012145.3 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr15:45433154 G>A maps to NM_175940.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:45448006 G>A maps to NM_175940.1 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MG-AAMC-01A-11D-A41K-08 chr15:45453997 C>A maps to NM_175940.1 R1307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DQ-01A-11D-A377-08 chr15:45387751 C>T maps to NM_014080.4 W1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:45404112 G>A maps to NM_014080.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:80016029 T>G maps to NM_022156.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr16:68104842 C>T maps to NM_017803.3 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr19:5790153 T>C maps to NM_020175.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:12630759 C>T maps to NM_030640.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:31059966 G>A maps to NM_152511.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:44703558 G>A did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:167095420 C>T maps to NM_001080426.1 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:89744488 G>A maps to NM_001946.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:1579037 G>A maps to NM_004420.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:1271545 G>A maps to ENST00000378888 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr1:1277186 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7132763 C>T maps to NM_004422.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr14:102474612 C>A maps to NM_001376.4 S1972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr14:102482729 C>T maps to NM_001376.4 S2506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:102494047 C>T maps to NM_001376.4 H3047H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr7:95705499 T>C maps to NM_004411.4 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr3:32571119 T>G maps to NM_016141.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr16:66770009 G>A maps to NM_006141.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr16:66770147 C>T did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:103090669 T>G maps to NM_001080463.1 L2953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:103124074 C>G maps to NM_001080463.1 L3375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr21:38862609 G>A maps to NM_001396.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:40316605 G>A maps to NM_004714.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr12:4722816 G>A maps to NM_003845.1 K487K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79792476 C>T maps to NM_001007533.3 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:207527851 G>A maps to NM_001093730.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr13:96239898 C>T maps to NM_198968.2 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr3:108347995 A>G maps to NM_014648.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:108391472 C>T maps to NM_014648.3 N853N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:108363629 T>C did not map to a codon.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr12:77419607 C>T maps to NM_203394.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:19251024 T>C maps to NM_024680.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr16:2284612 C>T maps to NM_004424.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr16:23555839 C>G maps to NM_001083614.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:25745378 C>A maps to NM_022659.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:25716009 G>A maps to NM_022659.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr10:131761765 C>T maps to ENST00000355311 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr23:48386619 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr3:183996102 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:139183809 G>A maps to NM_001195037.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr23:69253375 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr2:109545823 G>A maps to ENST00000376651 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr16:67914635 C>T maps to NM_014329.3 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr14:21215867 A>G maps to NM_006683.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:184692924 G>A maps to NM_025191.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:184695463 G>T maps to NM_025191.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139757757 C>T maps to NM_003792.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:57899382 C>T maps to NM_207033.1 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr4:148407184 C>T maps to NM_001957.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr4:148453711 A>G maps to NM_001957.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:85988973 C>T maps to ENST00000351625 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr20:62126424 C>T maps to NM_001958.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:207025332 T>C maps to NM_021121.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62327563 G>A maps to ENST00000378019 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr19:3984158 C>A maps to NM_001961.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr16:22260090 C>T maps to NM_013302.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr16:22260136 G>T did not map to a codon.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr3:127981000 G>A maps to NM_021937.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr17:28380699 A>G maps to NM_198529.3 Q576Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:43930687 G>A maps to NM_022785.3 Y1371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:64022883 G>A maps to NM_032437.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr2:56104956 G>A maps to NM_001039349.1 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65635812 G>A maps to NM_016938.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:22069323 T>C maps to NM_152726.2 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:19921209 G>A maps to NM_144715.3 H805H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:52285246 G>A maps to NM_018100.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:52357120 T>C maps to NM_018100.3 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr23:44171918 T>C did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr2:233546302 C>T maps to NM_025202.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr8:132966121 T>C maps to NM_015137.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:132962329 C>T maps to NM_015137.3 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:132991263 C>T maps to NM_015137.3 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:23828654 C>T maps to NM_005864.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr14:23828663 T>G maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr14:23828669 T>G maps to NM_005864.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:42929863 C>T maps to NM_004247.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:110902096 G>A maps to NM_001963.4 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:13635865 G>A did not map to a codon.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr7:55229297 C>T maps to NM_005228.3 C535C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:55221777 G>A maps to NM_005228.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41307259 C>T maps to NM_053046.2 D261D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:34419697 G>A maps to NM_022073.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:137803631 G>A maps to NM_001964.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:137803313 C>T maps to NM_001964.2 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr10:64573203 G>A maps to NM_001136178.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr2:73518809 G>A maps to NM_001965.3 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr2:63101582 G>A maps to NM_015252.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:63175804 C>A maps to NM_015252.3 Y643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr11:65343823 G>A maps to NM_001099409.1 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:64622146 C>T maps to NM_006795.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:31484533 G>A maps to NM_014600.2 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42193241 C>T maps to NM_139265.3 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr11:125450014 C>A maps to ENST00000278903 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr15:40313179 A>G maps to NM_001013703.2 K1418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:124106407 C>T maps to NM_001414.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:36358238 C>T maps to NM_012199.2 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:141567319 C>T maps to NM_012154.3 Q298Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr8:141567247 G>A maps to NM_012154.3 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr8:141570541 G>A maps to NM_012154.3 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:141572637 G>A maps to NM_012154.3 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr1:36474312 T>C maps to NM_024852.2 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr1:36307351 G>A did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr23:24075811 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:2409151 G>A maps to ENST00000314800 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr19:10226165 G>A maps to NM_003755.3 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr1:32690026 C>T maps to NM_003757.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr22:38254722 C>G maps to ENST00000262832 Y180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:32610272 G>A maps to NM_006360.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:32610620 C>T maps to NM_006360.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7481550 C>T maps to NM_001416.2 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr3:71745610 C>T maps to NM_001134651.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:72179742 C>T maps to NM_004096.4 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:184039640 G>A maps to NM_001194947.1 E430E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr1:21205815 C>G maps to NM_001198801.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:21143946 G>A maps to NM_001198801.1 R1465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr7:73604628 C>T maps to NM_022170.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr14:103807367 C>T maps to NM_183004.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:852990 G>A maps to NM_001972.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:11565664 C>T maps to NM_001420.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:50661329 G>A maps to NM_021952.3 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr4:139980683 G>C maps to ENST00000379550 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr23:129208568 A>C did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:129200818 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:37771286 G>A maps to NM_052906.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr12:96641091 C>T maps to NM_005230.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr7:36910036 G>A maps to NM_014800.9 C622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:37136299 C>T maps to NM_014800.9 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr20:45003940 G>T maps to ENST00000439931 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67234422 G>A maps to NM_024712.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:141471405 C>T maps to NM_153702.3 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:11664578 G>A maps to NM_032377.3 C78C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr4:110972802 T>C maps to NM_024090.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S0-01A-11D-A41K-08 chr4:111119468 A>T maps to NM_024090.2 L8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr4:110972796 C>T maps to NM_024090.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr18:33739978 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:28017843 A>G maps to NM_018091.5 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:31653918 C>A maps to ENST00000395934 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:49724056 C>T maps to NM_198449.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr23:153609502 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48456919 G>A maps to NM_001166131.1 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1825079 C>T maps to NM_001010865.1 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A66V-01A-21D-A30E-08 chr22:29628272 C>T maps to NM_133455.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr2:27305359 C>T maps to NM_007046.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr2:27305293 C>T maps to NM_007046.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr18:2892374 G>A maps to NM_032048.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:2891120 C>T maps to NM_032048.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr20:39990960 G>A maps to NM_052846.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr14:89148372 T>C maps to ENST00000380664 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr14:89154653 C>T maps to ENST00000380664 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr12:13367624 A>T maps to NM_001423.2 *158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr19:14883283 C>T maps to NM_013447.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:14887553 G>C maps to NM_013447.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr19:14774335 G>A maps to NM_032571.3 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr19:14772883 G>A maps to NM_032571.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:119303005 G>A maps to NM_004098.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr7:155255150 G>A maps to NM_001427.3 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr4:71508118 A>C maps to NM_031889.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr5:73932280 C>T maps to NM_003633.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr1:8923005 T>C did not map to a codon.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr4:83378115 G>T maps to NM_021204.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr13:43872564 C>A maps to NM_001127615.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:129813661 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:111441444 C>T maps to NM_001977.3 N550N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:132203594 C>T maps to NM_006208.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:132195476 A>G maps to NM_006208.2 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr8:120575110 C>A maps to NM_006209.3 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:120598436 C>T maps to NM_006209.3 W504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:120631536 C>T maps to NM_006209.3 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:97625944 C>T maps to NM_001098175.1 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:40457491 G>A maps to NM_001248.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:23290498 C>T maps to NM_004901.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:23297338 C>T maps to NM_004901.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr20:25195564 C>T maps to NM_001247.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:101455822 C>T maps to NM_020354.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr3:27760934 A>T maps to ENST00000449599 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:41536146 C>T maps to NM_001429.3 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr12:132466836 G>T maps to ENST00000333577 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr12:132445685 C>T maps to ENST00000333577 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:132446495 C>T maps to ENST00000333577 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:132502187 C>T maps to ENST00000333577 G1380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:29314299 A>G maps to NM_001166005.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:29362426 G>A maps to NM_001166005.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr6:131216166 C>T maps to NM_001431.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr18:5395092 C>T maps to NM_012307.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr2:120932464 A>G maps to NM_020909.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:37988561 C>T maps to NM_017549.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:143091382 G>T maps to NM_005232.4 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:143095460 G>A maps to NM_005232.4 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:143096396 G>A maps to NM_005232.4 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:143097137 C>T maps to NM_005232.4 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:38188715 C>A maps to NM_001099439.1 G653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:38227056 G>A maps to NM_173641.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr3:89468540 G>T did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:89444999 C>A maps to NM_005233.5 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr2:222301118 C>T maps to NM_004438.3 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:222347369 G>A maps to NM_004438.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:66242774 G>A maps to NM_004439.5 C599C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:66356359 C>T maps to NM_004439.5 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr6:94120324 C>T maps to NM_004440.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:94066492 A>G maps to NM_004440.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr1:22924680 C>T maps to NM_020526.3 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr1:22927491 G>T maps to NM_020526.3 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr3:134670793 C>T maps to NM_004441.4 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:134911532 G>C maps to NM_004441.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr3:134885816 C>T maps to NM_004441.4 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:134670842 C>T maps to NM_004441.4 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr1:23111123 G>T maps to ENST00000400191 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:23234627 C>T maps to ENST00000400191 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr1:23219447 C>T maps to ENST00000400191 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr1:23111210 C>T maps to ENST00000400191 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:184297349 C>T maps to NM_004443.3 D629D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:142562445 C>T maps to NM_004445.3 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:142564788 C>T maps to NM_004445.3 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:15342603 G>A maps to NM_001142886.1 H104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:48614288 C>T maps to NM_017957.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DQ-01A-11D-A377-08 chr17:48616672 C>T maps to NM_017957.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr7:100320665 T>G maps to NM_000799.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr7:100320381 G>A maps to NM_000799.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr8:144940743 G>A maps to NM_031308.1 I2226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr8:144941922 C>T maps to NM_031308.1 T1833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144940341 G>A maps to NM_031308.1 D2360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144940800 C>T maps to NM_031308.1 T2207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144945927 G>A maps to NM_031308.1 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144946857 C>T maps to NM_031308.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:220213573 G>A maps to NM_004446.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:51826840 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:16514561 C>T maps to ENST00000455140 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:720195 G>A maps to NM_022772.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:110299663 A>G maps to NM_139053.1 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr17:37881013 T>C maps to NM_004448.2 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:37881049 G>A maps to NM_004448.2 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:65344583 C>T maps to ENST00000506030 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:65372214 C>T maps to ENST00000506030 N1352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr12:56492615 C>T maps to NM_001982.2 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:56487294 C>T maps to NM_001982.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:212251656 C>A maps to NM_005235.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr2:212288966 G>A maps to NM_005235.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:128050245 G>A maps to NM_000122.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr10:50666943 G>A maps to NM_000124.2 R1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:50669576 G>A maps to NM_000124.2 H1268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:50740992 G>A maps to ENST00000515869 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr23:71425374 C>G did not map to a codon.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr21:39755837 G>A maps to NM_001136154.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:34135184 G>A maps to ENST00000447986 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:642502 G>A maps to NM_207332.1 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr8:37602101 G>A maps to NM_007175.6 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr1:43296725 C>T maps to NM_018538.3 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr17:62133143 C>T maps to NM_001433.3 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:62130707 C>T maps to NM_001433.3 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr16:23716454 C>T maps to NM_033266.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:23712399 G>A maps to NM_033266.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:23707240 G>A maps to NM_033266.3 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr1:236399659 G>A maps to NM_019891.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr18:19154389 T>A maps to NM_052911.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr18:19153549 G>A maps to NM_052911.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:19110306 C>T maps to NM_052911.2 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr8:27645491 T>C maps to NM_001017420.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:27633929 T>C maps to NM_001017420.2 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr20:13695682 T>C maps to NM_016649.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr5:54281324 C>G maps to NM_007036.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr12:53663406 C>T maps to NM_012291.4 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:53666574 T>G maps to NM_012291.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:53680239 C>T maps to NM_012291.4 N1240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:6488404 C>T maps to NM_031475.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr6:152420001 G>A maps to NM_001122741.1 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr6:152265312 C>T maps to NM_001122741.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr14:64701761 G>A maps to NM_001437.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95676989 C>G maps to NM_017697.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:64081762 G>A maps to NM_004451.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64074902 C>T maps to NM_004451.3 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr23:103498922 G>A did not map to a codon.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr12:56532055 G>A maps to NM_001184796.1 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr2:67631094 G>A maps to NM_019002.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:137848592 G>A maps to NM_004730.2 R198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:44015715 C>T maps to NM_014297.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr21:40190388 G>A maps to NM_005239.4 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr21:40193594 C>T maps to NM_005239.4 D387D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:13949323 G>T maps to NM_004956.4 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr7:13975391 G>A maps to NM_004956.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:157105281 T>A maps to NM_001145312.1 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr1:157068524 C>T maps to NM_001004341.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:41611324 G>A maps to NM_001079675.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr12:12037451 G>A maps to NM_001987.4 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr4:5735119 C>T maps to NM_153717.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr4:5721042 C>A maps to NM_153717.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:5755632 G>A maps to NM_153717.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr4:5691058 C>T maps to NM_147127.4 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:5564751 G>A maps to NM_147127.4 G1250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr1:92979230 C>T maps to NM_005665.4 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr17:74006444 G>C maps to NM_001988.2 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74019735 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:69704571 C>T maps to NM_001193363.1 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr4:56768604 A>G maps to NM_018261.3 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr4:56726616 C>T maps to NM_018261.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:457048 C>T maps to ENST00000315013 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67221639 C>T maps to NM_178516.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:133580443 C>T maps to NM_021807.3 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr1:231471574 C>T maps to NM_175876.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:231471745 C>T maps to NM_175876.3 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:11158105 G>A maps to NM_001001998.1 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:122723879 A>C maps to NM_001034194.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:108384688 A>G maps to NM_015065.2 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr8:119122901 G>C maps to NM_000127.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:28574583 G>A maps to NM_001440.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr8:28573785 G>A maps to NM_001440.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:72211429 G>A maps to NM_000503.4 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:45797812 C>T maps to ENST00000360649 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:66205252 A>T maps to ENST00000370616 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr6:66204898 A>C maps to ENST00000370616 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr6:66115186 G>A maps to ENST00000370616 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr6:66115237 T>G maps to ENST00000370616 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr6:6224991 T>C maps to NM_000129.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:6305755 C>T maps to NM_000129.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr6:6197459 G>A maps to NM_000129.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr1:197030038 T>A maps to NM_001994.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:197008542 T>A did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:197032023 A>G maps to NM_001994.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:197009751 C>A maps to NM_001994.2 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:197030912 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:76028838 C>T maps to NM_001992.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr19:17000462 C>T maps to NM_003950.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:169483631 G>A maps to ENST00000367796 S2203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr1:169493104 A>T maps to ENST00000367796 G1947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:169511012 T>C maps to ENST00000367796 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr13:113772751 C>T maps to NM_000131.3 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:113770091 C>T maps to NM_000131.3 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr23:154182173 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:138630552 C>T did not map to a codon.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr23:57458437 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:57515243 C>T did not map to a codon.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:61574166 C>T maps to NM_013402.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:61570337 C>T maps to NM_013402.4 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:51048294 G>A maps to NM_007051.2 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:175933900 G>T maps to NM_014613.2 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr15:80472566 G>A maps to NM_000137.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:293239 G>A maps to NM_182705.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:14687627 A>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:1880950 G>A maps to NM_031213.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:74489561 G>A maps to NM_016014.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:111801180 C>T maps to NM_001177996.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr2:45550 G>A maps to NM_001077710.2 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:58919680 A>G maps to NM_198847.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr11:58893555 T>C maps to NM_198947.3 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:47629001 G>A maps to NM_138371.1 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50752651 G>A maps to NM_001001794.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr22:50754486 G>A maps to NM_001001794.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:45726575 G>A maps to NM_017911.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:208478147 C>T maps to ENST00000272839 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr9:96320950 C>T maps to ENST00000333936 C947C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr6:170627924 C>T maps to NM_032448.1 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:170626691 C>T maps to NM_032448.1 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:54185949 A>G did not map to a codon.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr9:71395166 C>G maps to NM_138333.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr13:25744274 G>T maps to NM_152704.2 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr13:25743972 T>C maps to NM_152704.2 P595P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr23:63412938 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:63410417 C>T did not map to a codon.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr2:131521765 G>A maps to NM_001105195.1 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr2:131520256 G>T maps to NM_001105195.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr13:51825913 C>T maps to NM_145019.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:17533144 C>A maps to NM_138401.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr7:22985645 A>G maps to NM_032581.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:201846108 G>A maps to NM_173822.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr23:134166692 T>A did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr23:92964855 G>A did not map to a codon.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr8:139278044 G>A maps to NM_015912.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr8:139209801 C>T maps to NM_015912.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr8:139144958 C>A maps to NM_015912.3 V1366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr8:139190873 C>T maps to NM_015912.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr8:139263142 C>A maps to NM_015912.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:139323132 C>T maps to NM_015912.3 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr4:89671666 G>C maps to NM_014883.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:89912188 C>T maps to NM_014883.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr4:89702351 T>C maps to NM_014883.2 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:137277735 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:137284781 G>A maps to NM_016603.2 D652D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr10:61011333 C>T maps to ENST00000435852 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr1:55077405 C>T maps to NM_176782.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:18928481 G>A maps to NM_153707.2 C331C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:108518287 C>T maps to NM_001080396.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:6245334 C>T maps to NM_032127.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:79629649 C>T maps to NM_016010.2 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr8:79598724 T>C maps to NM_016010.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr21:35757885 A>G maps to NM_058182.4 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:140139875 C>T maps to NM_001001710.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:74091852 A>G did not map to a codon.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr15:98995216 G>A maps to NM_182562.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:118970009 G>A maps to ENST00000420106 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:118970051 G>A maps to ENST00000420106 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr10:15325964 C>T maps to NM_001010924.1 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:15254958 C>T maps to NM_001010924.1 W876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr10:15255015 G>A maps to NM_001010924.1 H857H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr10:15255870 G>A maps to NM_001010924.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:15255000 G>A maps to NM_001010924.1 D862D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:15256020 C>T maps to NM_001010924.1 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:15256155 G>A maps to NM_001010924.1 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:93217229 A>G maps to NM_032042.5 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:99871329 C>T maps to NM_198507.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr1:36788015 C>T maps to NM_018166.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:102709873 T>C maps to NM_001136123.1 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr2:29259408 C>G maps to NM_199280.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr2:29237324 T>C maps to NM_199280.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:119295630 G>A maps to NM_024581.4 N959N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr19:35718887 G>A maps to NM_152481.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr17:18708851 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18694223 G>A maps to NM_016078.4 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr17:15406354 C>A maps to NM_145301.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:15457127 C>T maps to NM_145301.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr4:91229662 T>C maps to NM_001145065.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:91645132 G>A maps to NM_001145065.1 V667V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr4:91230658 A>G maps to NM_001145065.1 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr4:2648483 C>T maps to ENST00000324666 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr10:128973612 G>A maps to NM_001039762.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr10:128973672 C>T maps to NM_001039762.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:128973690 C>T maps to NM_001039762.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:159091854 G>A maps to NM_001128424.1 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr23:103432834 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr23:103420366 A>G did not map to a codon.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr10:46248087 G>A maps to ENST00000399588 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:97088127 G>A maps to NM_017561.1 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:110592991 C>T maps to NM_033088.2 C639C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr23:34150169 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr23:34150303 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr23:34148191 C>A did not map to a codon.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr23:34149501 A>T did not map to a codon.
Sequencing variant TCGA-V1-A8MK-01A-11D-A364-08 chr23:34149301 G>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr23:34962548 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr23:34962847 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr23:34961793 T>C did not map to a codon.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr23:34960973 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr23:34961837 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:34961470 G>T did not map to a codon.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr23:34961837 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr23:37027784 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr23:37026829 C>T did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr23:37027155 C>G did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr23:37027274 G>T did not map to a codon.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr23:37027374 C>T did not map to a codon.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr23:37028424 A>G did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:37028756 C>T did not map to a codon.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr23:37028250 C>T did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr23:37028159 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:37027834 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:37027855 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:37028325 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr8:130867924 G>T maps to NM_016623.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr6:3850734 C>T maps to NM_012135.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr6:3850539 C>G maps to NM_012135.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr3:101535762 G>A maps to NM_145037.2 E349E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr18:29867773 G>A maps to ENST00000269209 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:29848727 G>A maps to ENST00000269209 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:29850313 T>C maps to ENST00000269209 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:29867950 G>A maps to ENST00000269209 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:177250450 G>A maps to NM_021165.2 Q713Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:190068209 G>A maps to NM_199051.1 N413N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr15:59064094 T>G maps to NM_001040450.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:49236608 G>A maps to NM_080829.2 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr23:119419024 G>A did not map to a codon.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr13:114514744 C>T maps to NM_182614.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:212799338 G>T maps to NM_153606.3 G374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr5:156590507 C>G maps to NM_130899.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:50979131 G>A maps to ENST00000391816 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr7:128312528 T>C maps to NM_001012454.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:131832159 C>T maps to NM_032809.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr9:131831377 G>A maps to NM_032809.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr9:40702846 C>A maps to NM_001083124.1 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr9:43627186 C>T maps to NM_001145196.1 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr9:43627099 T>C maps to NM_001145196.1 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr9:90535289 T>C maps to NM_001145124.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr9:90535985 G>A maps to NM_001145124.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:134136238 C>T maps to NM_033387.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr8:87486551 G>A maps to NM_016033.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:124195407 C>A maps to NM_032899.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:54735286 T>C maps to NM_001010872.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr20:37580706 G>A maps to NM_030919.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:49107167 G>A maps to NM_017708.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49113194 G>A maps to NM_017708.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr17:18874965 G>A maps to NM_001039999.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr8:144810217 G>A maps to NM_198488.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:5140530 C>T maps to NM_201400.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65341081 G>A maps to NM_001098785.1 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr6:17608510 C>T maps to NM_016255.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:85135864 G>A maps to ENST00000393246 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr15:64365168 T>C maps to NM_032231.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr2:33820567 G>A maps to ENST00000395190 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr16:89831296 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:89805298 G>A maps to NM_000135.2 H1417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr23:14883151 C>A did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr23:14861808 C>A did not map to a codon.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr23:14863073 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr3:10128871 T>A maps to NM_033084.3 C1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:45639924 T>G maps to NM_020937.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr14:45645391 C>T maps to NM_020937.2 D1145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:99091368 C>T maps to NM_005766.2 D784D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:242401942 G>A maps to NM_014808.2 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr2:223499163 C>T maps to NM_005687.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:223489481 G>A maps to NM_005687.3 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr17:80041236 C>T maps to NM_004104.4 E1802E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:170428527 T>C maps to NM_024622.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr20:3128063 C>T maps to NM_021826.4 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr4:187540590 G>A maps to ENST00000260147 L2386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr4:187540698 G>A maps to ENST00000260147 T2350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:187531071 G>A maps to ENST00000260147 D3320D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:187629094 C>T maps to ENST00000260147 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr5:150911163 G>A maps to NM_001447.2 R3265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr5:150922323 T>C maps to NM_001447.2 G2788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr5:150922047 G>A maps to NM_001447.2 H2880H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A723-01A-12D-A32B-08 chr5:150917381 C>T maps to NM_001447.2 A3055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150887066 G>A maps to NM_001447.2 A4055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150901350 G>A maps to NM_001447.2 N3601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150945294 C>T maps to NM_001447.2 E1066E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:92570899 C>T maps to ENST00000298047 V3432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:92088334 C>A maps to ENST00000298047 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr11:92086738 G>A maps to ENST00000298047 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr11:92568222 C>T maps to ENST00000298047 D3353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr11:92086236 G>A maps to ENST00000298047 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:92534269 C>T maps to ENST00000298047 H2697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L2-01A-31D-A41K-08 chr11:92085829 C>T maps to ENST00000298047 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr11:92086087 T>C maps to ENST00000298047 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr11:92590446 C>A maps to ENST00000298047 V3811V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr4:126372550 A>G maps to NM_024582.4 G3460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371607 T>A maps to NM_024582.4 L3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371767 T>C maps to NM_024582.4 Y3199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr4:126242059 C>G maps to NM_024582.4 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr4:126336324 T>C maps to NM_024582.4 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:126373018 G>A maps to NM_024582.4 T3616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr4:126319976 A>T maps to NM_024582.4 P1738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr4:126411434 G>C maps to NM_024582.4 G4486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr4:126367459 C>T maps to NM_024582.4 I2402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:126241421 C>T maps to NM_024582.4 Q1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:126336669 C>T maps to NM_024582.4 G2184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:126369941 G>T maps to NM_024582.4 G2591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:126371284 G>A maps to NM_024582.4 T3038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:126372316 A>G maps to NM_024582.4 R3382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr19:40331090 C>T maps to NM_001436.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:45944610 C>T maps to ENST00000348697 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr3:13659705 C>T maps to NM_001165035.1 C620C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr15:48707833 A>G maps to NM_000138.4 N2650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr15:48773909 T>C maps to NM_000138.4 S1302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr15:48791236 T>A did not map to a codon.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr15:48779509 G>A maps to NM_000138.4 I1154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr5:127710363 A>G maps to NM_001999.3 C684C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:8212298 G>A maps to NM_032447.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr19:8188378 G>A maps to NM_032447.3 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr19:8161783 C>T maps to NM_032447.3 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr19:8137033 C>T maps to NM_032447.3 P2662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr19:8130922 A>C maps to NM_032447.3 P2770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:8152024 A>G maps to NM_032447.3 G2230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:5541626 C>T maps to ENST00000312577 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr3:33400491 C>T maps to NM_012157.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:33415376 C>T maps to NM_012157.3 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:15936754 C>T maps to NM_012304.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:15936787 C>T maps to NM_012304.3 C323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:37541446 G>A maps to NM_012166.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:48059589 C>T maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr18:71790684 G>A maps to NM_001142958.1 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:5948525 G>A maps to NM_032807.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:5955733 C>T maps to NM_032807.3 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:5960416 C>T maps to NM_032807.3 H743H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr7:100190515 T>C maps to NM_012172.4 C261C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39521715 C>T maps to NM_178820.3 W175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr6:146125918 A>C maps to NM_032145.4 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:39871007 G>A maps to NM_203301.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:55817902 A>G maps to NM_152231.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:147813011 C>T maps to NM_205836.1 H893H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:16577178 G>A maps to NM_018994.1 R714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr1:16641763 C>A maps to NM_018994.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16577178 G>A maps to NM_018994.1 R714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:101154163 C>T maps to NM_001029860.3 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr19:46215457 G>A maps to NM_001080469.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:11733378 G>C maps to NM_018438.5 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr5:171299982 C>A maps to NM_012300.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139835725 G>A maps to NM_018998.2 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:12800211 G>A maps to ENST00000380339 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:207133069 A>G maps to NM_001170631.1 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:40411865 C>T maps to NM_003890.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr19:40357400 C>A maps to NM_003890.2 T5304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:40433638 C>T maps to NM_003890.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr19:40421658 G>A maps to NM_003890.2 C754C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:40398444 G>A maps to NM_003890.2 G2174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:40362964 C>A maps to NM_003890.2 V5035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr19:40395883 G>A maps to NM_003890.2 R2505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr1:161479820 C>A maps to NM_001136219.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:161642792 G>T maps to NM_004001.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:72370578 G>T maps to NM_138782.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:141029927 G>A maps to ENST00000354789 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr1:157648601 G>A maps to NM_052939.3 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:157666076 G>A maps to NM_052939.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:157558992 C>G did not map to a codon.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:157559033 G>A maps to NM_031282.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:157504476 T>C maps to NM_031281.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:11667247 G>A maps to NM_004462.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr11:111745900 A>G maps to NM_138378.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:111747584 G>A maps to ENST00000428306 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr17:72858968 A>C maps to ENST00000442102 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr17:72862612 G>A maps to ENST00000442102 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:114861009 A>G maps to NM_020177.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:114879004 C>T maps to NM_020177.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr11:61563273 C>T maps to NM_004111.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr11:61563279 C>A maps to NM_004111.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:124988245 G>A maps to NM_001039112.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr14:53325132 C>A maps to NM_001134999.1 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr14:53331154 C>T maps to NM_001134999.1 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:91433507 G>A maps to NM_002005.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:121943287 G>A maps to NM_001024613.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr7:121942293 G>A maps to NM_001024613.2 N395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35850517 C>T maps to NM_005304.3 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr19:35849908 C>T maps to NM_005304.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr4:155507878 G>A maps to NM_000508.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr4:155509999 A>G maps to NM_000508.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr4:155487687 A>G maps to NM_005141.4 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr23:54481901 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:54475339 T>C did not map to a codon.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr6:36993602 A>G maps to NM_173558.3 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr9:95784667 A>C maps to NM_033086.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:95796899 C>T maps to NM_033086.2 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:32764088 T>C maps to NM_139241.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46E-01A-31D-A257-08 chr23:76711784 A>T did not map to a codon.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr23:76711831 C>A did not map to a codon.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr5:170876178 C>T maps to NM_003862.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:4479655 C>T maps to NM_020638.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:4479679 G>A maps to NM_020638.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr11:69625453 G>A maps to NM_005247.2 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr15:49716686 A>T maps to NM_002009.3 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr15:49776571 A>C maps to NM_002009.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:167416733 C>T maps to NM_007045.2 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:27109594 T>C did not map to a codon.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr10:123325039 G>A maps to ENST00000351936 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr10:123325039 G>A maps to ENST00000351936 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr4:1808051 C>T maps to NM_000142.4 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:1018243 C>T maps to NM_021923.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr4:155532985 T>C maps to ENST00000407946 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:60073566 C>T maps to NM_001113411.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr7:76828504 T>A maps to NM_006682.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr4:153897502 G>A maps to NM_033393.2 P1020P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr23:135290739 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:67264378 G>A maps to NM_013241.2 Y963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:67264086 G>A maps to NM_013241.2 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:133799130 C>A maps to NM_001145106.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr9:133779561 G>A maps to NM_001145106.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:133780630 G>A maps to NM_001145106.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr11:27016183 C>T maps to NM_203371.1 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr23:15373391 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:71012723 T>C maps to NM_001004311.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:164466568 G>C maps to NM_018086.2 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr3:99649663 G>C maps to NM_001042459.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:56109063 G>A maps to NM_032836.2 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:39973357 C>A maps to NM_021939.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39974443 C>T maps to NM_021939.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr7:30054371 T>C maps to NM_017946.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr12:2909555 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:152275292 A>G maps to NM_002016.1 D4023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:152281969 G>T maps to NM_002016.1 R1798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr1:152279918 C>T maps to NM_002016.1 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr1:152282807 A>G maps to NM_002016.1 H1518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:152275877 C>T maps to NM_002016.1 S3828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr1:152280683 G>C maps to NM_002016.1 G2226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr1:152277017 G>A maps to NM_002016.1 S3448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:152284790 G>A maps to NM_002016.1 H857H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr11:128680405 C>T maps to NM_002017.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr14:21542131 G>A maps to NM_018071.3 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:21541328 C>T maps to NM_018071.3 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:21543038 C>T maps to NM_018071.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr8:142490101 G>A maps to NM_207414.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr9:84607229 T>C maps to NM_001001670.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr23:153587626 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:153587695 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr23:153588854 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr3:58156416 C>T maps to NM_001164317.1 G2610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46E-01A-31D-A257-08 chr3:58062899 G>A maps to NM_001164317.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:58108881 C>T maps to NM_001164317.1 I1063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr3:58097608 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:58064442 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:58107208 G>A maps to NM_001164317.1 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:58109157 C>T maps to NM_001164317.1 S1155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:128488071 C>T maps to NM_001458.4 D1510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr7:128484280 G>A maps to NM_001458.4 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OA-01A-11D-A41K-08 chr7:128481308 G>A maps to NM_001458.4 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:128480707 C>T maps to NM_001458.4 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:128485187 C>A maps to NM_001458.4 T1223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:128491584 C>T maps to NM_001458.4 T1915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:86088043 G>A maps to NM_013231.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr20:14306919 A>G maps to NM_198391.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr13:28919629 C>T maps to NM_002019.4 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:29001982 G>A maps to NM_002019.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr13:28610091 C>T maps to NM_004119.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr13:28608022 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:28601283 C>T maps to NM_004119.2 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr5:180048620 G>A maps to NM_182925.4 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr5:180030326 C>T maps to NM_182925.4 R1319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:76107351 G>A maps to NM_017791.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:33359689 G>A maps to NM_001103184.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr1:240371600 C>T maps to ENST00000406993 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr1:240370946 G>A maps to ENST00000406993 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:240370964 G>A maps to ENST00000406993 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr17:43311098 G>A did not map to a codon.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr12:50041124 G>T maps to NM_175736.4 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:171251206 A>G maps to NM_002021.1 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr1:171086251 C>T maps to NM_006894.5 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:146684989 G>A maps to NM_001461.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203316789 C>T maps to NM_002023.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr23:147024666 G>A did not map to a codon.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr2:216259361 G>A maps to NM_212482.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr2:216289829 G>A maps to NM_212482.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:80696417 G>A maps to NM_022158.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:80678198 G>A maps to NM_024619.3 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr6:159653388 G>A maps to NM_032532.2 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:159653199 G>A maps to NM_032532.2 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr6:159653361 G>A maps to NM_032532.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr1:109268474 G>A maps to NM_001144937.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:131052272 G>A maps to NM_133372.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr5:131008039 T>C maps to NM_133372.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:159790452 C>T maps to ENST00000379346 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:159782885 C>T maps to ENST00000379346 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr8:42932434 G>A maps to NM_002027.2 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:49186292 C>T maps to NM_004476.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr11:71850177 G>T maps to ENST00000442948 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr11:94039856 G>A maps to NM_001080486.1 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr14:38060571 A>C maps to NM_004496.2 *473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr14:38061622 G>A maps to NM_004496.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A66V-01A-21D-A30E-08 chr14:38060701 G>A maps to NM_004496.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:38061876 G>A maps to NM_004496.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:22563480 G>A maps to NM_021784.4 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:60297911 C>T maps to NM_012182.2 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr6:1611153 C>T maps to NM_001453.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:86602197 G>A maps to NM_005251.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr5:72743455 G>T maps to NM_004472.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr2:114256920 C>T maps to NM_012184.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:70918905 C>T maps to NM_199135.4 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr6:1390757 G>A maps to NM_001452.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr14:29237876 G>A maps to NM_005249.3 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:169533416 C>T maps to NM_012188.4 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr1:42657163 C>T maps to NM_001198850.1 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:2983404 G>A maps to NM_202002.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:26851603 C>T maps to NM_003593.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr14:89878583 C>T maps to NM_001085471.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:71096125 G>A maps to NM_032682.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:71096126 C>A maps to NM_032682.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr3:71037203 G>A maps to NM_032682.4 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr3:71027138 C>T maps to NM_032682.4 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr7:114269987 G>A maps to NM_148898.3 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr7:114269984 A>G maps to NM_148898.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:41545741 C>T maps to NM_001012426.1 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr6:1313421 G>A maps to NM_033260.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr23:55651013 T>G did not map to a codon.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr23:55650283 C>T did not map to a codon.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr22:36897390 G>A maps to NM_001102371.1 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:130570835 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:74670867 C>T maps to NM_003838.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr4:79334178 G>A maps to NM_025074.6 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:79396693 C>T maps to NM_025074.6 T2595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:79240096 G>A maps to NM_025074.6 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:14808118 G>A maps to ENST00000380880 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr13:39262557 T>C maps to NM_207361.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:39261855 G>A maps to NM_207361.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr13:39451251 A>G did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr13:39451252 G>T did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr13:39433449 C>T maps to NM_207361.4 Y2414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr13:39263437 C>T maps to NM_207361.4 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr13:39438592 T>G maps to NM_207361.4 P2611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:190862185 A>T maps to NM_004477.2 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:85863021 G>A maps to NM_174938.4 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:13743456 C>T maps to NM_018027.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr23:131219960 G>A did not map to a codon.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr23:131212857 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:131219625 C>A did not map to a codon.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr9:37740870 C>G maps to NM_014907.2 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr23:12736536 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:12704239 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:41738968 G>A maps to NM_006653.3 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr13:32761790 C>T maps to NM_023037.2 R1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr4:48551611 C>T maps to NM_015030.1 W1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr4:48611010 G>A maps to NM_015030.1 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr17:79496147 C>T maps to NM_001077182.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:4323366 C>T maps to NM_024333.2 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:120130763 G>A maps to NM_007085.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr4:162577599 A>G maps to NM_020116.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr4:162697125 G>A maps to NM_020116.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:162680659 G>A maps to NM_020116.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr4:162307447 G>A maps to NM_020116.3 C665C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr4:162307015 G>T maps to NM_020116.3 Y809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:47556898 C>T maps to ENST00000397748 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr5:121188191 C>T maps to NM_177478.1 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr5:121187963 C>T maps to NM_177478.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:121188335 G>A maps to NM_177478.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr16:53913759 C>G maps to NM_001080432.2 S327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:53913790 C>T maps to NM_001080432.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr6:37426393 C>T maps to NM_015050.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:24180990 G>T maps to NM_000147.4 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr6:143828560 C>T maps to NM_032020.4 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr16:70508757 C>T maps to NM_145059.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr16:70506484 A>G maps to NM_145059.2 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr23:154282920 G>C did not map to a codon.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr15:91422744 C>T maps to NM_002569.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr19:49207085 C>T maps to NM_001097638.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr19:49207193 G>T maps to NM_001097638.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49206449 C>T maps to NM_001097638.2 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr11:94277394 G>T maps to NM_002033.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr9:139925557 G>A maps to NM_004479.3 C211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr14:66208992 G>C maps to NM_178155.1 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:96651186 C>T maps to NM_006581.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50310484 G>A maps to NM_025129.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:7495580 T>C maps to NM_004860.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7496150 C>T maps to NM_004860.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr19:35613745 G>T maps to NM_021910.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr5:39119723 A>G maps to ENST00000263405 N726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr3:46009700 A>G maps to NM_024513.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr3:197497067 G>A maps to NM_032288.6 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:90895850 C>T maps to NM_003505.1 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:130648818 C>T maps to NM_007197.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:130647903 C>T maps to NM_007197.3 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:42636102 G>A maps to NM_001466.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42635478 C>T maps to NM_001466.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636060 C>G maps to NM_001466.3 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636210 C>T maps to NM_001466.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636498 C>T maps to NM_001466.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:42636312 G>A maps to NM_001466.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr8:28385110 A>T maps to NM_017412.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662612 G>A maps to NM_012193.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662879 G>A maps to NM_012193.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86663023 G>A maps to NM_012193.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:86662966 C>T maps to NM_012193.2 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr11:86665902 G>C maps to NM_012193.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr8:104337699 C>T maps to NM_003506.3 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:104336879 G>A maps to NM_003506.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr10:35929634 C>A maps to NM_031866.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:72849209 C>T maps to NM_003508.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:72849638 C>T maps to NM_003508.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:3532473 G>A maps to NM_001136198.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr14:31066654 C>T maps to NM_017769.3 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr4:76573855 G>A maps to NM_203505.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:77961317 G>A maps to NM_080491.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr23:153940642 G>C did not map to a codon.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr22:17443634 G>A maps to NM_001037814.1 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr22:17444668 C>T maps to NM_001037814.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:29599356 C>T maps to NM_001470.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr23:151514067 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr4:47405708 T>G maps to NM_000812.3 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:47428007 C>T maps to NM_000812.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr23:151138737 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr23:151124291 C>G did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr23:151138817 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:151123858 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr23:151131068 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr4:46067499 T>C maps to NM_173536.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:27725916 C>T maps to NM_033223.4 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:170235670 C>A maps to NM_014211.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr23:151821285 G>A did not map to a codon.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr6:89888604 T>G maps to NM_002042.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr2:171693378 G>A maps to NM_000817.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:26581401 C>T maps to NM_001134366.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr10:26575383 C>T maps to NM_001134366.1 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr10:26575311 C>G maps to NM_001134366.1 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr10:26559615 C>T maps to NM_001134366.1 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:26562620 C>T maps to NM_001134366.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr3:30885876 A>G did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr23:49355892 C>G did not map to a codon.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr4:870994 C>T maps to NM_005255.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:844869 G>A maps to NM_005255.2 Q1171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:853454 C>T maps to NM_005255.2 W1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr4:887224 C>T maps to NM_005255.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr4:845556 C>A maps to NM_005255.2 G1163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr22:30951158 G>A maps to NM_004861.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:24124220 G>A maps to NM_001008216.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr5:153765899 C>T maps to NM_198321.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr9:101608263 C>T maps to NM_024642.3 F488F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr9:101608341 T>C maps to NM_024642.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:155098656 C>T maps to NM_052917.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr2:31165136 G>A maps to NM_024572.2 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr2:31155003 G>A maps to NM_024572.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:230338964 C>T maps to NM_004481.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:230372098 C>T maps to NM_004481.3 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:166611441 G>A maps to NM_004482.3 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:166613679 A>G maps to NM_004482.3 H423H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr12:51754522 G>A maps to NM_007210.3 N383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:4874639 G>A maps to NM_017417.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:69800216 G>A maps to NM_020692.2 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr3:16261010 A>G maps to NM_054110.4 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr11:11362458 G>A maps to NM_198516.2 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr4:173873357 C>T maps to NM_001034845.2 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62396360 C>T maps to NM_198335.2 W709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62397884 C>A maps to NM_198335.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr15:42602621 G>A maps to NM_198141.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr15:42631921 C>A maps to NM_198141.2 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr15:42598784 A>G maps to NM_198141.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:6645759 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:130111297 C>T maps to NM_032293.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr21:34903823 C>A maps to NM_001136006.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:34894555 G>A maps to NM_001136006.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:29708153 G>A maps to NM_152236.1 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:34072055 C>A maps to NM_139285.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr12:101018419 C>T maps to NM_174942.1 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:9820568 G>A maps to NM_201433.1 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:9830017 G>A maps to NM_201433.1 C318C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr17:39871694 C>T maps to NM_000805.3 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chr23:48650527 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:61041508 G>T maps to NM_080473.4 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr19:19576171 C>T maps to ENST00000404158 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr1:153790535 G>A maps to NM_020699.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr1:153788812 G>C maps to NM_020699.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B2-01A-12D-A32B-08 chr12:120897760 G>C maps to NM_176818.2 *137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:155206158 G>A maps to NM_001005742.2 H367H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35740293 G>A maps to NM_020944.2 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:22737811 A>G maps to NM_020973.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:104128501 C>T maps to NM_004193.2 C961C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr10:104140415 G>T maps to NM_004193.2 E1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:89522749 G>A maps to NM_002053.2 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:89587610 G>C maps to NM_004120.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:89480251 G>A maps to NM_018284.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr1:89659074 C>T maps to NM_052941.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:89847451 G>A maps to NM_198460.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr4:72623866 T>C maps to ENST00000504199 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:13008630 C>T maps to NM_000159.2 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr2:163005634 G>A maps to ENST00000233604 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr7:44185093 A>G did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr2:27746164 A>T maps to NM_001486.3 L579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr6:53010373 A>G maps to NM_003643.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:120615276 G>A maps to NM_006836.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr12:120621407 C>T maps to NM_006836.1 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr12:120568994 C>T maps to NM_006836.1 A2519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:120569760 C>T maps to NM_006836.1 E2461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:120575042 G>A maps to NM_006836.1 G2248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:120613961 G>A maps to NM_006836.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr9:79117308 G>A maps to NM_001097636.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr6:10529593 T>A maps to NM_145649.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr6:10556755 C>T maps to NM_001491.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr6:10586308 G>A maps to NM_145655.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr5:74325283 C>T maps to NM_016591.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr8:75276268 C>T maps to NM_018972.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:7842905 G>T maps to NM_020634.1 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:97156823 C>T maps to NM_001001557.2 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153669518 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:37815941 G>A maps to NM_001190468.1 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30116255 C>T maps to NM_024307.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:75150997 G>A maps to NM_030792.6 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr17:649821 G>A maps to NM_015721.2 Y487Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr17:650796 G>A maps to NM_015721.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr5:154270985 G>C maps to NM_015465.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:45593395 C>T maps to NM_024707.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr1:92944267 T>G maps to NM_005263.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:135863746 C>T maps to NM_004188.4 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:74056730 T>C maps to NM_032380.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr6:13365847 G>A maps to NM_018988.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67719372 G>A maps to NM_030819.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:179740881 G>A maps to NM_005110.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr5:179740917 G>A maps to NM_005110.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:118030616 C>T maps to NM_005264.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:23497418 G>A maps to NM_015044.4 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:85778162 C>T maps to NM_000821.4 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr19:38876986 A>G maps to NM_152657.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:34912922 C>T maps to NM_024835.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:34934520 G>A maps to NM_024835.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:34945825 G>A maps to NM_024835.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:34913158 A>G maps to NM_024835.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr1:235505066 C>T maps to NM_001037277.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr22:24622216 C>A maps to NM_001099781.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:33440319 G>A maps to NM_178026.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr10:85904773 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr3:10331493 C>T maps to NM_016362.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr11:59608633 A>G maps to NM_005142.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:59609964 G>A maps to NM_005142.2 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:100280925 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100279356 G>A maps to NM_022574.4 S1031S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100282478 G>A maps to NM_022574.4 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:233621022 C>T maps to ENST00000373566 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr2:233655741 G>T maps to ENST00000373566 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:150417943 C>T maps to NM_130759.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr7:150439448 C>T maps to ENST00000447239 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr7:150174546 C>T maps to NM_175571.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr1:147230322 G>A maps to NM_005266.5 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr1:147380381 C>T maps to NM_005267.4 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr1:35226968 G>A maps to NM_153212.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr1:35227196 G>A maps to NM_153212.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:20797511 G>A maps to NM_001110221.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr17:42882369 C>G maps to NM_001080383.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:228345725 G>A maps to NM_020435.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr23:30737630 G>C did not map to a codon.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr4:80329309 C>T maps to NM_033214.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr2:69173529 C>G maps to NM_182536.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:33099743 G>A maps to NM_000404.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr11:134240924 C>T maps to NM_138342.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:134181018 G>A maps to NM_001080407.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr11:134151336 G>C maps to NM_001080407.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr15:69553492 A>T maps to NM_015554.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr9:6554736 G>A maps to NM_000170.2 H749H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr9:6536171 C>T maps to NM_000170.2 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51676021 G>A maps to NM_181789.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr15:51696485 C>T maps to NM_181789.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:131267152 C>T maps to NM_001003722.1 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr9:131296230 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:121746684 C>T maps to NM_005270.4 D1065D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr2:121746843 C>T maps to NM_005270.4 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:121746948 C>T maps to NM_005270.4 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:36162401 C>T maps to NM_022343.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr1:53975546 T>G maps to NM_147193.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr9:3828280 G>A maps to NM_001042413.1 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:38652181 C>T maps to NM_006708.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr17:663479 T>G did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr23:14748514 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:14627240 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr12:56868363 G>A maps to NM_013267.2 C396C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr12:56868872 T>C maps to NM_013267.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr1:183933080 C>T maps to NM_015101.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:183938607 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:104390557 G>A maps to NM_031302.3 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:48183473 G>A maps to NM_015711.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr23:120182501 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr23:120182328 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr1:182355538 T>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:58722739 G>A maps to NM_080661.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr11:58604620 T>G maps to NM_145016.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:58602078 G>A maps to NM_145016.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr6:1624709 G>A maps to NM_001500.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:19748734 C>A maps to NM_016573.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19746241 G>A maps to NM_016573.2 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:49759675 G>A maps to NM_013334.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49760428 G>A maps to NM_013334.2 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:16254790 A>G did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:16279024 C>T maps to NM_006877.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr14:24702731 C>A maps to ENST00000348719 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:155649576 C>T maps to NM_003875.2 Y528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr19:3150223 C>T maps to NM_002068.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr20:57415469 C>T maps to NM_016592.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr20:57415577 C>T maps to NM_016592.2 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:23465563 C>T maps to NM_002073.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:1722001 C>T maps to NM_002074.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:100275275 C>T maps to NM_005273.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr6:30520935 G>T maps to NM_005275.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:68610373 G>T maps to NM_000406.2 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr9:131027884 C>T maps to NM_004486.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr12:100551033 C>G maps to ENST00000266746 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr12:133353578 C>A maps to NM_005895.3 E1274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:133351741 G>A maps to NM_005895.3 R1376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:133384772 G>A maps to NM_005895.3 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr15:74368248 G>A maps to NM_001038640.2 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr15:72954611 G>A maps to NM_018652.4 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr15:75562494 G>T maps to NM_001164404.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:99623790 C>T maps to NM_001010917.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:121413150 T>C maps to ENST00000393667 E2073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr3:121383371 T>C maps to ENST00000393667 L3255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:88650292 A>G maps to ENST00000376023 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:155721806 C>T maps to ENST00000368331 V2139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr1:155735540 G>C maps to ENST00000368331 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr3:39141918 A>G maps to NM_031899.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:45012588 A>G maps to NM_001012511.1 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr3:194118888 C>T maps to NM_004488.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr1:167038354 C>T maps to NM_005814.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr2:96689179 G>A maps to NM_207328.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:96690301 C>T maps to NM_207328.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr19:33584365 C>T maps to NM_018025.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:33608947 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr1:27226495 A>T maps to NM_022078.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:241402906 C>T maps to NM_002081.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:241401797 G>A maps to NM_002081.2 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr23:132887601 G>C did not map to a codon.
Sequencing variant TCGA-EJ-A7NJ-01A-22D-A34U-08 chr23:132458206 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr23:132437322 T>A did not map to a codon.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr13:92345963 G>A maps to NM_004466.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:95034756 G>A maps to NM_005708.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:5550837 C>T maps to NM_019593.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr12:50498485 G>A maps to NM_005276.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:63784458 G>A maps to ENST00000314140 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:67578598 C>T maps to NM_020806.4 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr19:34887246 A>G maps to NM_000175.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr23:48970824 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr23:48973488 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:24473883 G>A maps to NM_001503.2 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr6:24463023 C>T did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:13798049 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:13792707 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:27216197 T>C maps to NM_018066.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr7:23300354 A>G maps to ENST00000435486 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr7:23286529 A>C maps to ENST00000435486 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:136113732 C>T did not map to a codon.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr9:132853234 A>C maps to NM_001136557.1 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr19:6734269 G>A maps to NM_001080452.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr19:6731107 G>A maps to NM_001080452.1 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr12:123186915 G>A maps to NM_177551.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr6:46973589 C>T maps to ENST00000283297 K853K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr6:47650244 G>A maps to NM_153839.6 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:47649197 C>T maps to NM_153839.6 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr23:135431328 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:135429591 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr23:135485422 G>A did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr23:135405106 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr23:135428547 A>G did not map to a codon.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr23:135487898 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:135428887 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:135426828 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:26534168 G>A maps to NM_001145168.1 H809H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr16:57608858 A>T maps to ENST00000349457 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:46821803 C>T maps to NM_015234.4 T1322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:46830831 C>T maps to NM_015234.4 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:46851337 G>T maps to NM_015234.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr23:129518742 C>G did not map to a codon.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr23:129519054 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:129518839 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:129519097 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:27333934 G>A maps to NM_005288.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr10:95326920 G>T maps to NM_181745.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:134942934 T>C maps to ENST00000368577 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:37697697 G>A maps to NM_032777.9 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:37698930 G>A maps to NM_032777.9 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:22390047 C>T maps to NM_145290.2 T1082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MG-AAMC-01A-11D-A41K-08 chr4:22390724 C>T maps to NM_145290.2 R903R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr4:22389681 G>A maps to NM_145290.2 N1204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr4:22414906 G>A maps to NM_145290.2 N710N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr3:100368588 C>T maps to NM_032787.2 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr14:105518071 G>A maps to NM_013345.2 C134C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:131498746 C>T maps to NM_198827.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:131602981 C>T maps to NM_198827.3 Y698Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:53100611 C>T maps to NM_001099652.1 R354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:20043983 G>T maps to NM_001002911.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr17:72363724 T>C maps to NM_181790.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:131487315 G>T maps to NM_207364.2 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr3:119962485 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:9171451 G>A maps to NM_024980.4 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr10:25887197 C>T maps to NM_020752.2 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr10:25887054 C>T maps to NM_020752.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:168074013 G>A maps to NM_153832.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:128408803 G>A maps to NM_005291.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr23:78426886 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:125797090 C>T maps to NM_005294.1 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr10:125426387 G>A maps to NM_153442.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr1:27720643 C>T maps to NM_005281.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr1:202092722 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr19:46094785 C>A maps to NM_005282.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:105858890 C>T maps to NM_007227.3 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr23:150348253 G>A did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr23:150348880 T>C did not map to a codon.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr23:150345371 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr23:150349722 C>T did not map to a codon.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr23:150349742 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:19037718 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:123214175 C>T maps to NM_032554.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr12:54757586 G>A maps to NM_020370.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr16:57718005 C>T maps to NM_170776.4 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:57719788 G>A maps to NM_170776.4 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:90106487 C>T maps to NM_032119.3 F5137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr5:90083964 C>T maps to NM_032119.3 S4577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:89933654 T>C maps to NM_032119.3 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr5:89992871 C>T maps to NM_032119.3 S2688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OA-01A-11D-A41K-08 chr5:90149292 G>A maps to NM_032119.3 E5799E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr5:89990011 G>A maps to NM_032119.3 W2480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:101910581 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:101912704 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr23:101972034 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:101969963 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr23:101971614 C>A did not map to a codon.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr12:13061953 G>A maps to NM_003979.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr10:47000208 C>T maps to NM_014696.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr17:80013938 G>A maps to NM_212492.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr17:7217478 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:109465124 T>C maps to NM_013296.4 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:46943651 C>T maps to NM_133443.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:1106406 C>T maps to NM_002085.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:53072579 C>T maps to NM_015696.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr19:35512474 G>A maps to NM_020895.3 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35510428 G>A maps to NM_020895.3 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr22:40366976 C>T maps to NM_004810.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:40365470 C>T maps to NM_004810.2 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:11750978 C>T maps to NM_014668.3 C944C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:240656718 C>T maps to NM_022469.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:24676594 C>G maps to NM_021180.3 Y564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:24673991 G>A maps to NM_021180.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr5:153144158 G>A maps to NM_001114183.1 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr5:153144044 C>A maps to NM_001114183.1 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr5:153056636 T>G maps to NM_001114183.1 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr5:152870477 C>T maps to NM_001114183.1 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:158257611 C>T maps to NM_000826.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:122616695 A>C did not map to a codon.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr11:105845209 G>A maps to NM_001077243.2 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:105483075 C>T maps to NM_000829.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr11:105797469 C>T maps to NM_000829.3 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr11:105789610 C>A maps to NM_000829.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:87407078 G>A maps to NM_017551.2 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr4:94344040 C>T maps to NM_001510.2 Y489Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:94344061 C>T maps to NM_001510.2 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr21:30963506 C>T maps to ENST00000327783 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:30927537 C>T maps to ENST00000327783 W814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr1:37267463 A>T maps to NM_000831.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:37316001 G>A maps to NM_000831.3 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:42569513 C>T maps to NM_002088.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:140043501 G>A maps to ENST00000371546 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr16:9858033 C>A maps to NM_000833.3 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr16:10274037 G>A maps to NM_000833.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr16:9858511 G>A maps to NM_000833.3 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:13717456 G>T maps to NM_000834.3 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:13716715 G>A maps to NM_000834.3 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr12:13716214 C>T maps to NM_000834.3 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:72843503 G>A maps to NM_000835.3 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr9:104432659 C>T maps to NM_133445.2 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:1005551 G>A maps to NM_138690.1 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:14545075 C>A maps to ENST00000507975 E991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176857945 C>T maps to NM_002082.3 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176860982 C>T maps to NM_002082.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr6:146480671 C>T maps to NM_000838.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr6:146480671 C>T maps to NM_000838.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr6:146350829 C>T maps to NM_000838.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:146720091 C>T maps to NM_000838.3 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:51746688 C>T maps to NM_000839.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:86468359 C>T maps to NM_000840.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:34100898 C>T maps to NM_000841.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr6:34003798 G>A maps to NM_000841.1 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:7340479 C>T maps to NM_181874.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr7:126882811 G>A maps to NM_001127323.1 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr7:126086369 A>T maps to NM_001127323.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr7:126746595 A>T maps to NM_001127323.1 Y227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:126746586 G>A maps to NM_001127323.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:126882823 G>A maps to NM_001127323.1 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr17:42428523 G>A maps to NM_002087.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr23:16142273 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:16170624 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:71693680 G>A maps to NM_002092.3 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr17:38133154 C>T maps to NM_178171.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:38062139 C>T maps to NM_001165958.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr17:38073350 C>T maps to NM_001165958.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr17:38062396 G>A maps to NM_001165958.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr8:144643540 C>T maps to NM_024736.6 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr8:144643206 G>A maps to NM_024736.6 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:27802747 G>C maps to NM_001109763.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:3628287 C>T maps to NM_031965.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MG-AAMC-01A-11D-A41K-08 chr19:42738595 G>A maps to NM_019884.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:42736821 G>A maps to NM_019884.2 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr3:119634999 G>A maps to NM_002093.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr9:124064267 G>T maps to NM_000177.4 E58*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-A9TH-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr9:124094712 T>A maps to NM_000177.4 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:110217412 C>G maps to ENST00000369830 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr22:24381722 G>A maps to NM_000853.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:24384212 G>A maps to NM_000853.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:28367778 G>A maps to NM_145657.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr4:54966543 C>A maps to NM_133267.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr1:89319012 A>T maps to NM_001514.5 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr8:30436472 G>A maps to NM_002095.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr8:30472223 A>G maps to NM_002095.4 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr19:6387479 G>C maps to NM_002096.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:6389528 G>A maps to NM_002096.2 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:18362865 A>G maps to NM_005316.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:73927218 C>T maps to NM_016328.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:73953040 G>A maps to NM_016328.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr7:74212377 T>C maps to NM_173537.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr16:27506670 C>T maps to NM_001520.3 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr16:27472772 G>A maps to NM_001520.3 D2076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr9:135553527 C>T maps to NM_012204.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:135554265 C>T maps to NM_012204.2 G420G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr6:111288986 G>A maps to NM_138408.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:111288818 C>T maps to NM_138408.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr10:1044995 G>A maps to NM_012341.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:60773004 C>T maps to NM_015666.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr11:106810482 C>T maps to ENST00000282249 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr12:14766077 G>A maps to NM_004963.3 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:14804928 A>G maps to NM_004963.3 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7907407 C>T maps to NM_000180.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr23:108718894 G>C did not map to a codon.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr23:108719046 G>C did not map to a codon.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr23:108641816 G>A did not map to a codon.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr3:73016752 C>T maps to NM_001080393.1 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:145038027 G>A maps to NM_002099.6 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr14:25101105 C>T maps to ENST00000382542 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:14927706 G>A maps to NM_177925.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr11:118966002 C>T maps to NM_002105.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:31944875 C>T maps to NM_001013699.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr2:26492859 G>A maps to NM_000183.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr17:39881380 G>A maps to ENST00000310778 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr5:82940275 C>A maps to NM_001884.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr15:89424630 G>A maps to NM_178232.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr15:89430418 G>A maps to NM_178232.2 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19371691 G>A maps to NM_023002.2 Y138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:46637657 G>A maps to NM_173811.3 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:69148910 C>A maps to NM_005329.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:172822330 T>C maps to NM_003642.3 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr18:43685266 C>T maps to NM_138443.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:2242667 A>G maps to NM_024511.5 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:19058262 G>A maps to NM_017645.3 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr23:152721737 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:156514160 G>A maps to NM_032782.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5248218 G>A maps to NM_000518.4 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:5289794 A>T maps to NM_005330.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr23:153224169 A>C did not map to a codon.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr23:153222852 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr23:153216819 T>C did not map to a codon.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr23:153216311 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153216312 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153220569 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr12:104487294 T>G maps to NM_013320.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:104476380 C>T maps to NM_013320.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:30659554 C>T maps to NM_002110.3 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:45262493 C>T maps to NM_021072.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr5:45645595 C>T maps to NM_021072.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr5:45262466 C>T maps to NM_021072.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr5:45303941 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:45262079 G>T maps to NM_021072.2 S872S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr1:155255753 G>T maps to NM_020897.1 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:155254436 G>A maps to NM_020897.1 W326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr6:55142194 T>C maps to NM_001526.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:13542246 C>T maps to NM_024827.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr5:141009252 G>C maps to NM_003883.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr23:48674946 T>G did not map to a codon.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr23:48674947 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr23:48673410 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:48190905 C>T maps to NM_015401.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr23:71787744 G>C did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr23:71708812 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr7:18687445 G>A maps to NM_178425.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:4496342 C>T maps to ENST00000301284 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:7023870 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:6968395 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:242169567 G>A maps to NM_005336.3 Y1197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:83724078 G>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:236760201 C>G maps to NM_018072.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:236746391 G>A maps to NM_018072.5 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:73989700 G>A maps to ENST00000334988 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr14:31765177 G>A maps to ENST00000389961 I1846I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:31763121 C>A maps to ENST00000389961 L1930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr2:37255198 A>G maps to NM_019024.1 F1240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr2:37284596 G>A maps to NM_019024.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:58121388 C>T maps to NM_022070.4 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr17:58143747 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:13140126 G>A maps to NM_015987.4 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr10:93253265 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:45469959 A>G maps to NM_024602.5 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr7:43484981 C>T maps to NM_015052.3 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr7:43484654 G>A maps to NM_015052.3 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:43483841 C>T maps to NM_015052.3 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:43484780 C>T maps to NM_015052.3 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:43540348 G>A maps to NM_015052.3 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:124731626 G>A maps to NM_020733.1 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:66725337 A>G maps to NM_033647.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:65124823 C>T maps to NM_014877.3 R1110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr17:65083152 G>A maps to NM_014877.3 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:50609160 A>G maps to NM_016173.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr11:124793826 T>G maps to NM_152722.4 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:92848480 G>A maps to ENST00000453812 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:65413404 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:65483508 A>G did not map to a codon.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr15:64047507 G>C maps to ENST00000261887 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:63984646 T>C maps to ENST00000261887 E1931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:64005613 T>C maps to ENST00000261887 R1467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr15:63991136 G>A maps to ENST00000261887 S1565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr15:28463680 G>A maps to NM_004667.4 C1994C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:28386875 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:28369236 G>A maps to NM_004667.4 L4378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:28483298 C>T maps to NM_004667.4 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:28483802 C>T maps to NM_004667.4 K1231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:28502368 G>A maps to NM_004667.4 G785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr15:28437220 C>A maps to NM_004667.4 L2779L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:89577166 C>T maps to NM_014606.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:89574197 G>A maps to NM_014606.1 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr10:69748521 T>G maps to NM_022079.2 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:89363500 T>C maps to NM_017912.3 H986H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr17:80400434 A>T maps to NM_173620.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:126080680 C>T maps to NM_012259.2 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr6:126080680 C>T maps to NM_012259.2 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:91843737 T>A maps to NM_001017975.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:91781958 C>A maps to NM_001017975.3 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr1:91859786 G>A maps to NM_001017975.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr3:120365111 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:81381466 G>A maps to NM_000601.4 Y198Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr7:81339551 T>G maps to NM_000601.4 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:3446573 C>T maps to ENST00000511533 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:79657218 C>A maps to NM_004712.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79657239 C>T maps to NM_004712.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79667774 G>A maps to NM_004712.4 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:210522366 C>T maps to NM_001170580.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:210796907 C>T maps to NM_001170580.1 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:210637879 C>T maps to NM_001170580.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:210591652 C>T maps to NM_001170580.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:210847633 G>A maps to NM_001170580.1 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:100123402 C>T maps to NM_001127258.1 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr1:222713412 G>T maps to NM_024746.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:108072520 G>A maps to NM_007072.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:97218566 G>A maps to NM_032558.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr7:27565970 G>A maps to NM_152740.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:21800812 G>A maps to NM_015094.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:62200949 T>C maps to ENST00000394997 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:62207831 A>G maps to ENST00000394997 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:119002675 C>G maps to NM_198971.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr12:123333378 C>A maps to NM_003959.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:114510460 T>C maps to ENST00000426820 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:114499302 C>T maps to ENST00000426820 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:114512766 G>A maps to ENST00000426820 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:139268746 G>A maps to NM_022740.4 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr7:139285233 G>A maps to NM_022740.4 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr7:139416758 G>A maps to NM_022740.4 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr11:33373267 T>C maps to NM_005734.3 H974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr11:33308013 T>C maps to NM_005734.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr6:25726458 G>A maps to NM_170745.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:26033604 C>T maps to NM_003513.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr6:27101128 G>A maps to NM_021064.4 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr6:26184298 C>T maps to NM_003523.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:27114511 C>T maps to NM_080593.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr6:27861557 G>A maps to NM_003527.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:26031877 T>C maps to NM_003537.3 *137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr6:26045769 G>A maps to NM_003531.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr6:27777904 C>A maps to NM_003536.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr6:26189196 G>A maps to NM_003539.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr6:26285589 T>G maps to NM_003543.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr6:143092406 G>A maps to NM_006734.3 Q1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr6:143074326 A>G maps to NM_006734.3 L2420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:143092709 G>A maps to NM_006734.3 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr1:41976592 C>T maps to NM_024503.3 S2250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr10:71139677 C>T maps to ENST00000439900 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:71055390 T>C maps to ENST00000439900 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr5:176310789 G>A maps to NM_002115.2 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176310870 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:71002998 C>T maps to NM_025130.3 D251D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr10:71025574 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr6:32714044 G>A maps to NM_020056.4 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr6:30459139 G>C maps to NM_005516.5 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr21:38311177 T>C maps to NM_000411.5 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:148760004 A>T maps to NM_003071.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:186055462 T>G maps to NM_031935.2 G2990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:186009010 G>A maps to NM_031935.2 Q2060Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr1:185834880 T>C maps to NM_031935.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:185931776 C>T maps to NM_031935.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:185987440 T>C maps to NM_031935.2 N1809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr1:185959467 C>T maps to NM_031935.2 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr1:186106991 C>T maps to NM_031935.2 R4604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr1:186064438 C>T maps to NM_031935.2 T3453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr1:185939491 A>T maps to NM_031935.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:186056761 C>T maps to NM_031935.2 H3116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr1:186088389 G>A maps to NM_031935.2 A3972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr1:186056777 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr1:186063455 C>A maps to NM_031935.2 A3415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr1:186024594 C>T maps to NM_031935.2 S2311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:186143766 C>A maps to NM_031935.2 P5312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:24147062 G>C maps to NM_000191.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:74646120 G>A maps to NM_000859.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr5:74641423 T>C maps to NM_000859.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr5:43293007 A>T maps to NM_002130.6 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:1068741 C>T maps to NM_012292.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:162910327 G>A maps to NM_001142556.1 W580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr12:121435349 C>T maps to NM_000545.5 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:36093662 G>C maps to NM_000458.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr20:43056984 C>T maps to ENST00000338692 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr8:76463689 C>T maps to NM_004133.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:138759637 T>C maps to NM_006895.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr1:12907827 G>A maps to NM_001013631.1 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:83280637 C>A maps to NM_031370.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:43882501 G>A maps to NM_001098204.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr23:100667604 A>G did not map to a codon.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:39334539 A>G maps to ENST00000221419 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:23650123 T>C maps to ENST00000414299 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr1:23637360 G>C maps to ENST00000414299 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41808628 C>T maps to NM_007040.3 Q583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:38818745 G>C maps to NM_138394.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr4:57522052 G>C maps to NM_032495.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:27148261 G>A maps to NM_153631.2 Q202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:27169056 G>A maps to NM_002141.4 H250H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr7:27204580 T>A maps to NM_152739.3 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr17:46622153 C>G maps to NM_002145.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr17:46620855 C>T maps to NM_002145.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr17:46627824 C>T maps to NM_002146.4 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:46628487 G>A maps to NM_002146.4 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:46700276 C>T maps to NM_024017.4 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr12:54403268 C>A maps to NM_022658.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr2:176965062 G>A maps to NM_021193.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:177034057 C>T maps to NM_006898.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:177036308 G>A maps to NM_006898.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:177036518 G>A maps to NM_006898.4 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr2:176987555 C>A maps to NM_014213.3 Y20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:21103088 C>G did not map to a codon.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr1:45793569 G>A maps to NM_032756.2 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:45792870 C>T maps to NM_032756.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr4:175416698 C>A maps to NM_000860.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35551572 C>T maps to NM_182983.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr11:18313151 T>C maps to NM_181507.1 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:534268 C>T maps to NM_005343.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr11:63257731 G>T maps to NM_054108.3 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr19:49657891 C>T maps to NM_002152.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49657621 G>A maps to NM_002152.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr3:186386776 G>A maps to NM_000412.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr5:175110244 C>A maps to NM_001131055.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr1:152192079 G>A maps to NM_001009931.1 Y675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr1:152192637 G>A maps to NM_001009931.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr1:152191167 C>T maps to NM_001009931.1 S979S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:152187857 G>A maps to NM_001009931.1 R2083*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:152192931 G>T maps to NM_001009931.1 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr1:152192358 A>T maps to NM_001009931.1 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr1:152187687 T>C maps to NM_001009931.1 R2139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr1:152187069 C>T maps to NM_001009931.1 E2345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:20818847 G>A maps to NM_022460.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr2:20824555 C>T maps to NM_022460.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:11401263 C>T maps to NM_005114.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr16:22926768 A>G maps to NM_006043.1 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr16:1961821 G>A maps to ENST00000454677 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:129026326 C>T maps to NM_004807.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr23:131762489 G>A did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:209879154 G>C did not map to a codon.
Sequencing variant TCGA-CH-5743-01A-21D-1576-08 chr11:43876381 C>A maps to NM_016142.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr9:99013717 G>A maps to NM_000197.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr5:118837733 A>G did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:120056907 C>A maps to ENST00000235547 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:119962119 C>T maps to NM_000198.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:119964453 C>A maps to NM_000198.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr16:30999230 C>T maps to NM_025193.3 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr8:145534872 C>T maps to NM_005526.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:145535420 C>T maps to NM_005526.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145535864 C>A maps to NM_005526.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:67199715 C>G maps to NM_001040667.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr17:56565350 G>A maps to NM_001080439.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr14:102548542 A>T maps to NM_001017963.2 L787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr6:44221298 C>T maps to NM_007355.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr10:118441314 G>T maps to NM_025015.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr10:118464681 C>T maps to NM_025015.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:118440696 C>T maps to NM_025015.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr6:31797487 C>G maps to NM_005346.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr14:65008202 C>T maps to NM_021979.3 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:65008445 C>T maps to NM_021979.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr4:128726277 C>T maps to ENST00000438626 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:128732694 C>T maps to ENST00000438626 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:128748470 G>A maps to ENST00000438626 Q716Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr5:137893675 C>A did not map to a codon.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr7:75933152 C>T maps to NM_001540.3 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr11:111784195 A>G maps to NM_001541.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:53752033 T>C maps to NM_006308.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:119617248 G>A maps to NM_014365.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:122459554 G>A maps to NM_024610.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr2:198353197 A>G maps to NM_199440.1 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:22172691 G>A maps to NM_005529.5 Y2791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:22161190 G>A maps to NM_005529.5 H3567H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:22168750 G>T maps to NM_005529.5 P3011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:22161367 G>A maps to NM_005529.5 F3508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:22179483 G>A maps to NM_005529.5 C2173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:22192251 G>A maps to NM_005529.5 G1424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:31724104 C>A maps to NM_006644.2 G375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr13:31727070 T>G maps to NM_006644.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:135593929 T>G did not map to a codon.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr23:135593231 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr1:23520100 C>T maps to NM_000864.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:87725480 C>A maps to NM_000865.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr6:87726041 G>A maps to NM_000865.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr13:47469887 G>A maps to NM_000621.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr23:113965912 G>A did not map to a codon.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr23:113965799 C>T did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr23:114082717 C>T did not map to a codon.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr23:113965772 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr23:113965813 A>C did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr11:113853982 G>T maps to NM_213621.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:183772515 C>T maps to NM_130770.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:154875944 G>A maps to NM_024012.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:154863322 C>T maps to NM_024012.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:20005665 G>A maps to NM_000871.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:92509038 G>A maps to NM_019859.3 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr10:124271536 A>G maps to NM_002775.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:38835667 T>C did not map to a codon.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr4:3234975 C>T maps to NM_002111.6 H2784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr4:3176834 G>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:3235011 C>T maps to NM_002111.6 D2796D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr21:33318387 G>A maps to NM_014586.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr7:48018174 C>A maps to NM_004507.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:53657924 T>C did not map to a codon.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr23:53618048 T>C did not map to a codon.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr23:53578097 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr23:53563400 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:53561000 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:53620386 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr23:53586377 G>C did not map to a codon.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr23:53576283 C>A did not map to a codon.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr23:53621470 T>C did not map to a codon.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr3:50340315 G>T maps to NM_153281.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:70934963 C>T maps to NM_032821.2 L2996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr16:70902477 G>A maps to NM_032821.2 R3768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:70867854 G>A maps to NM_032821.2 P4537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr16:70843712 T>A maps to NM_032821.2 T4951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr11:118919562 G>A maps to NM_001130991.1 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr1:220273971 T>C maps to NM_018060.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr1:220275730 T>A maps to NM_018060.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:82922422 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10394817 G>A maps to NM_000201.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:10398383 C>T maps to NM_001544.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr19:10398290 G>T maps to NM_001544.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:6294998 G>A maps to NM_012405.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:1068716 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:148585689 C>T did not map to a codon.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:159002390 T>A maps to ENST00000295809 Y413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr1:158984676 C>T maps to ENST00000295809 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr1:159021836 T>G maps to ENST00000295809 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:91177945 C>T maps to NM_012420.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr11:298629 C>T maps to NM_001025295.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr9:21239505 C>T maps to NM_002172.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr9:21228106 T>C maps to NM_021268.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr9:21186978 T>C maps to NM_021068.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr3:129185798 T>G maps to NM_052985.2 Y261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1573864 G>A maps to NM_014714.3 G1078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1630762 C>T maps to NM_014714.3 W507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr16:1639731 G>A maps to NM_014714.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:27688650 G>A maps to NM_015662.1 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr2:27677276 G>A maps to NM_015662.1 F1158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr20:42265849 G>A maps to NM_016004.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:42275595 T>C maps to NM_016004.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr20:42242495 C>A maps to NM_016004.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr3:107885799 A>G maps to ENST00000457963 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr13:21245110 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:69370143 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:69354562 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr15:65622152 C>T maps to NM_004884.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr15:65621730 G>A maps to NM_004884.3 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:65628160 C>T maps to NM_004884.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:65685845 G>A maps to NM_020962.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A723-01A-12D-A32B-08 chr15:65686764 G>A maps to NM_020962.1 Y566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:160494344 T>C maps to NM_000876.2 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:160482959 G>A maps to NM_000876.2 S1194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1841077 C>T maps to NM_001146006.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1842412 A>G maps to NM_001146006.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr1:201185717 C>T maps to NM_001164586.1 G3144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:68675743 C>T maps to NM_002180.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:68678938 C>T maps to NM_002180.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr19:51831964 G>A maps to NM_001101372.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr23:130419245 C>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:130408140 C>T did not map to a codon.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr23:130416522 T>G did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr3:151165278 A>G maps to NM_178822.4 D830D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:151166250 G>A maps to NM_178822.4 H506H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr3:118621498 G>A maps to NM_152538.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr11:18738273 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:18739553 G>A maps to NM_173588.3 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr1:117150672 G>A maps to NM_001542.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:117156480 G>A maps to NM_001542.2 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr16:21658766 T>C maps to NM_005849.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr1:159912789 G>A maps to NM_001135050.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr11:133790979 G>A maps to NM_014987.1 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr11:133790583 G>T maps to NM_014987.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr11:133814171 G>A maps to NM_014987.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:99020055 G>A maps to NM_153687.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr7:50444411 C>T maps to NM_006060.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:50467922 C>T maps to NM_006060.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:213886795 C>G maps to ENST00000342002 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:213921698 G>A maps to ENST00000342002 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr17:37985742 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:206944257 C>T maps to NM_000572.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:206944739 G>A maps to NM_000572.2 D62D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr11:117864124 G>A maps to NM_001558.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr21:34640774 A>G maps to ENST00000433395 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:159711353 G>A did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr3:159710860 A>G maps to NM_000882.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18193063 C>T maps to NM_005535.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr23:117895120 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:81585158 G>A maps to NM_172217.3 R561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:148756444 C>T maps to NM_014443.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:17583128 G>A maps to NM_014339.5 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:57131714 G>A maps to NM_017563.3 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:57132269 G>A maps to NM_017563.3 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr22:50437762 C>T maps to NM_001001694.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:103040430 C>T maps to NM_003853.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr2:103063566 C>T maps to NM_003853.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:103061729 G>A maps to NM_003853.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr2:103063626 G>A maps to NM_003853.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:206972298 G>A maps to NM_153758.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr2:113535635 G>A maps to NM_000575.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr2:113593794 T>C maps to NM_000576.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:113675254 G>A maps to NM_014439.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:102632416 G>A maps to NM_004633.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr2:102641115 C>T maps to NM_004633.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:102626273 C>T maps to NM_004633.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr3:190345112 A>G maps to NM_002182.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr23:29972718 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr23:29301247 C>T did not map to a codon.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr23:28807501 T>A did not map to a codon.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr23:104999296 G>T did not map to a codon.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr23:104728368 T>A did not map to a codon.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr23:104984611 C>A did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr1:207040804 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:136714373 C>T maps to NM_144717.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:123534003 A>G did not map to a codon.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr1:67724720 C>T maps to NM_144701.2 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr1:207072688 G>A maps to NM_001185156.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr1:207072829 G>A maps to NM_001185156.1 W71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:37524300 C>T maps to ENST00000406505 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr22:37524347 G>A maps to ENST00000406505 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:37524279 G>A maps to ENST00000406505 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:37539571 C>T maps to ENST00000406505 W64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:55204232 G>T maps to NM_139017.4 G499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr23:1501314 A>G did not map to a codon.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr23:1499969 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr23:1497570 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:1497613 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:1484094 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:27372110 C>T maps to NM_000418.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr5:55248075 A>C did not map to a codon.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr5:35876449 G>C maps to NM_002185.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:35876341 C>T maps to NM_002185.2 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:153635493 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr1:153635688 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:10789859 C>T maps to NM_017620.2 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr2:239090710 G>A maps to NM_030768.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:31484796 G>T maps to NM_144981.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr18:22008831 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr8:57878867 A>G maps to NM_017813.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:128034366 C>T maps to NM_000883.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:100964784 C>T maps to NM_016247.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr3:101023019 T>C maps to NM_016247.2 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:62393500 C>T maps to NM_176877.2 Q1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr1:62257042 T>C maps to NM_176877.2 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:62550223 G>A maps to NM_176877.2 T1427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:61914293 G>C maps to NM_001040694.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:61912667 G>A maps to NM_001040694.1 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:105179319 C>T maps to ENST00000252520 R922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:220439862 G>A maps to NM_002191.3 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr2:220437227 C>T maps to NM_002191.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr12:57843451 C>T maps to NM_005538.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:99182211 C>T maps to NM_001134224.1 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:99155419 C>T maps to NM_001134224.1 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:233990467 G>A maps to ENST00000359570 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr11:2182080 G>A maps to NM_001042376.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:2182030 C>T maps to NM_001042376.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:5185353 C>T maps to NM_007179.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:7125509 G>A maps to NM_000208.2 D1014D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:7166396 C>T maps to NM_000208.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:7267686 C>T maps to NM_000208.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:19682475 C>T maps to NM_018142.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr8:19690801 G>A maps to NM_018142.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr17:60003894 A>C maps to NM_020748.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:153732835 C>A maps to ENST00000428986 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62415760 C>T maps to NM_030628.1 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:62417077 C>T maps to NM_030628.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:212118152 C>T maps to NM_015434.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:28633368 G>A maps to NM_018250.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr8:28692855 C>A maps to NM_018250.3 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:128626837 A>G maps to NM_015693.3 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr9:103055172 T>C maps to NM_014425.2 D878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:61802185 T>C did not map to a codon.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr14:24651221 G>A maps to ENST00000458132 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr12:30790009 G>A maps to NM_006390.3 F867F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr9:95418827 C>T maps to NM_022755.5 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr9:95403026 G>A maps to NM_022755.5 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr2:237405942 G>A maps to ENST00000457693 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr2:237285744 C>A did not map to a codon.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr2:237402437 C>T maps to ENST00000457693 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:51897157 G>A maps to NM_203424.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr3:51897228 G>A maps to NM_203424.1 W113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:51864454 A>T maps to NM_001085479.1 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:197619591 G>A maps to NM_001134435.1 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr15:67664645 C>T maps to NM_001031715.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr15:91040569 C>T maps to NM_003870.3 Q1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:91009600 C>T maps to NM_003870.3 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:91025224 G>A maps to NM_003870.3 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156521861 G>A maps to NM_178229.4 R492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr23:153278062 C>T did not map to a codon.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:10251300 G>A maps to NM_001570.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:10255193 C>T maps to NM_001570.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:10219597 G>A maps to NM_001570.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:10276297 G>A maps to NM_001570.3 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:66620607 G>A maps to NM_007199.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr12:44180480 A>G did not map to a codon.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr19:46388639 A>G maps to NM_015649.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:50162973 G>A maps to NM_001571.5 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr6:397163 G>A maps to NM_002460.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr11:614246 C>T maps to NM_004031.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr16:85936701 T>C maps to NM_002163.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr16:85936653 A>C maps to NM_002163.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr16:85946825 G>A maps to NM_002163.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:85946825 G>A maps to NM_002163.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr14:24632647 G>A maps to NM_006084.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:24633986 C>T maps to NM_006084.4 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:44099376 G>A maps to NM_001007561.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:44099418 G>A maps to NM_001007561.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr19:44097044 G>A maps to NM_001007561.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr19:44096612 G>A maps to NM_001007561.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr2:227659845 T>G maps to NM_005544.2 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr23:107977560 C>G did not map to a codon.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr23:107975999 G>A did not map to a codon.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr5:3600021 G>C maps to NM_024337.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr5:3599421 C>T maps to NM_024337.3 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:2749499 G>A maps to NM_033267.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr16:54966501 A>G maps to NM_005853.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:55362954 G>A maps to NM_024335.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr16:55362690 G>A maps to NM_024335.2 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:949845 C>T maps to NM_005101.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr15:76632801 C>A maps to NM_145805.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr15:74467873 G>A maps to NM_201526.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr15:74467264 C>T maps to NM_201526.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr20:13251263 G>A maps to NM_080826.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr14:77948908 G>A maps to NM_199296.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr20:33033193 T>G maps to ENST00000262650 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr20:33068459 T>A maps to ENST00000262650 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:47189689 C>A did not map to a codon.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr16:314963 C>T maps to NM_032039.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:52201707 C>T maps to NM_181501.1 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr1:145532145 C>T maps to NM_003637.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:68628054 G>A maps to ENST00000423218 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:42455140 G>T maps to NM_000419.3 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48154744 C>T maps to NM_002204.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr2:182376433 T>C maps to NM_000885.4 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:54803280 G>T maps to NM_002205.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr12:56078883 G>A maps to ENST00000347027 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:56088267 G>A maps to ENST00000347027 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr10:15649741 G>T maps to NM_003638.1 R566R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:37860416 C>T maps to NM_002207.2 I1015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr16:31414871 C>T maps to ENST00000444228 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr16:31409183 G>T maps to ENST00000444228 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr17:3649105 G>A maps to NM_002208.4 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:3661128 G>A maps to NM_002208.4 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr16:30500699 C>A maps to NM_002209.2 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr16:30516581 G>A maps to NM_002209.2 P751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30506131 G>A maps to NM_002209.2 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr16:31289352 C>T maps to NM_001145808.1 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr16:31372439 G>A maps to NM_000887.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr16:31382412 G>A maps to NM_000887.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr16:31373160 G>A maps to NM_000887.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr21:46308728 C>T maps to NM_000211.3 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:63912519 A>G maps to ENST00000371092 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr17:73728051 C>T maps to NM_001005619.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:73729576 C>T maps to NM_001005619.1 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:73738693 C>T maps to NM_001005619.1 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:20418788 C>T maps to NM_002214.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr10:7780626 G>A maps to NM_002216.2 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr3:52840312 C>T maps to NM_002217.3 D649D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52850919 C>T maps to ENST00000485816 T822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:7618674 G>A maps to ENST00000256861 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr23:54783700 G>T did not map to a codon.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr23:54777746 G>T did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:160850468 C>T maps to NM_017625.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr23:78619049 T>C did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:231742221 C>T maps to NM_030926.4 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr1:226923860 G>A maps to NM_002221.3 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr19:41223696 T>C maps to NM_025194.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:4776851 A>G maps to ENST00000356617 G1782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:26572044 G>A maps to NM_002223.2 H2349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr12:26780981 G>A maps to NM_002223.2 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:33653960 C>T maps to ENST00000374316 N1933N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr21:35237514 C>T maps to NM_003024.2 D1317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:35257764 C>T maps to NM_003024.2 G1594G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:24427159 G>A maps to NM_006277.2 D1630D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr2:24526683 G>A maps to NM_006277.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr15:40707599 G>A maps to NM_002225.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:185269160 A>G maps to NM_006469.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr1:185267217 A>C maps to NM_006469.4 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr2:128263211 C>T maps to NM_017969.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:128262665 G>C maps to NM_017969.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr2:128262755 C>T maps to NM_017969.2 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:10628674 G>A maps to NM_000214.2 C551C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:105618059 G>A maps to NM_002226.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:65300334 A>C maps to NM_002227.2 Y1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S0-01A-11D-A41K-08 chr1:65311266 T>A maps to NM_002227.2 K682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:65303715 A>G maps to NM_002227.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:65309755 C>T maps to NM_002227.2 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:17950418 T>A maps to NM_000215.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:17943478 C>T maps to NM_000215.3 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:17946738 G>A maps to NM_000215.3 N636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr19:17950367 G>T maps to NM_000215.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr4:6087152 G>A maps to NM_001099433.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr10:133949432 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:133976843 C>A maps to NM_001105521.2 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:133949507 C>T maps to NM_001105521.2 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:133930933 C>T maps to NM_001105521.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:15497051 C>T maps to NM_004973.2 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:15512453 C>T maps to NM_004973.2 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:59965594 C>T maps to ENST00000356057 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr10:64967186 T>G maps to NM_032776.1 S1414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr10:64968221 A>G maps to NM_032776.1 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr10:64936220 G>A maps to NM_032776.1 Q2413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr10:64958387 A>G maps to NM_032776.1 F1792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:64952884 A>G maps to NM_032776.1 S1963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:64973445 C>T maps to NM_032776.1 A827A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:227920224 G>A maps to NM_023007.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42138156 G>A maps to NM_005090.3 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:733030 C>T maps to ENST00000293882 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr5:78587010 G>A maps to NM_152405.4 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr8:75233374 C>A maps to NM_020647.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr20:42788454 G>A maps to NM_020433.4 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr20:42815084 T>C maps to NM_020433.4 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr16:87678350 C>T maps to NM_020655.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr14:24040358 G>A maps to NM_032452.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:23444068 G>A maps to NM_032876.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:59247824 T>C maps to NM_002228.3 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr17:39912082 G>A maps to NM_021991.2 H717H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr17:39915086 G>A maps to NM_021991.2 C511C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:8553408 T>C did not map to a codon.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr23:8536356 G>A did not map to a codon.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr23:8555965 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:8502378 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:8522090 G>A did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr3:124132348 C>T maps to NM_001024660.3 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:124132333 C>T maps to NM_001024660.3 D786D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr3:124374510 G>T maps to NM_001024660.3 V1952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:124017681 C>T maps to NM_001024660.3 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr9:731263 A>C maps to NM_015158.2 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:11304608 G>A maps to NM_015493.6 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:62718879 G>T maps to NM_181712.4 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:20142837 A>G maps to NM_003884.4 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr18:44579364 T>C maps to ENST00000356157 Y62Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr1:15386728 C>T maps to NM_201628.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr3:127642851 C>T maps to NM_207335.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr3:127646681 T>C maps to NM_207335.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:41705279 G>A maps to NM_152903.4 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:41766370 G>A maps to NM_032138.4 R675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:5021062 C>T maps to NM_000217.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr1:111061226 C>T maps to NM_005549.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:111147038 C>T maps to NM_004974.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:111216033 G>A maps to NM_002232.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr1:111216383 G>A maps to NM_002232.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr1:111217281 C>T maps to NM_002232.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:111217005 C>T maps to NM_002232.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:111216458 G>A maps to NM_002232.3 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:49573388 G>A maps to NM_031886.2 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:156192554 G>T maps to NM_172159.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:156009905 C>T maps to NM_172159.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:7827735 G>T maps to NM_004732.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr20:47990860 G>A maps to NM_004975.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:47991511 G>T maps to NM_004975.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr11:17793786 G>A maps to NM_001112741.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:17757920 C>T maps to NM_001112741.1 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr11:17793358 G>T maps to NM_001112741.1 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr1:110768690 G>A maps to NM_004978.4 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:120381667 C>A maps to NM_012281.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:120385959 C>T maps to NM_012281.2 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:112525242 T>A maps to ENST00000315987 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:112318869 G>A maps to ENST00000315987 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr2:11053085 G>A maps to NM_002236.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr2:11053814 C>T maps to NM_002236.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:11052974 C>T maps to NM_002236.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr20:49626293 G>A maps to NM_002237.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr20:49626482 C>T maps to NM_002237.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr18:77624158 C>T maps to NM_012283.1 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr18:77659467 C>T maps to NM_012283.1 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr1:211093036 G>A maps to NM_172362.2 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:210857204 C>T maps to NM_172362.2 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:150643988 G>A maps to NM_000238.2 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:150654453 C>T maps to NM_000238.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr12:49934915 G>T did not map to a codon.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr17:40323994 G>A maps to NM_012285.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr17:40321506 G>A maps to NM_012285.2 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:63175049 G>A maps to NM_139318.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr14:63447802 G>A maps to NM_139318.3 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61619768 C>T maps to NM_030779.2 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr17:61615447 C>T maps to NM_030779.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr2:163279881 G>A maps to NM_033272.2 H706H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr2:163291771 G>A maps to NM_033272.2 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr2:163292034 G>A maps to NM_033272.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:163292017 G>A maps to NM_033272.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:17409275 G>A maps to NM_000525.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr17:68128239 C>T maps to NM_018658.1 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:155711422 G>A maps to NM_002239.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr22:38823054 C>G maps to NM_152868.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr11:128781512 G>T maps to NM_000890.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:128781962 C>T maps to NM_000890.3 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr11:128786545 C>T maps to NM_000890.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr21:39086715 C>T maps to NM_002240.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr21:38997474 C>A maps to NM_002240.2 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr12:21919124 G>A maps to NM_004982.2 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr14:88707089 G>A maps to NM_138318.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:90650707 C>T maps to NM_022054.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr10:118969533 C>A maps to NM_181840.1 Y293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:215368302 C>T maps to NM_001017425.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr2:26950775 C>T maps to NM_002246.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:64065642 C>T maps to ENST00000422670 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:64064396 G>A maps to ENST00000422670 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr6:39158872 G>A maps to NM_003740.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:38810913 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18092573 C>T maps to ENST00000222249 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr1:154841765 C>T maps to NM_002249.4 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FO-01A-21D-A364-08 chr1:154841693 G>A maps to NM_002249.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:44278576 C>T maps to NM_002250.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr11:2549249 T>C did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr20:62070977 G>A maps to NM_172107.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:62078120 C>T maps to NM_172107.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:133196584 G>A maps to NM_004519.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr8:99440308 G>T maps to NM_020697.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr8:99440248 C>A maps to NM_020697.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:99440614 C>T maps to NM_020697.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr8:99441253 C>T maps to NM_020697.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr9:138651632 G>A maps to ENST00000298480 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:196254843 C>T maps to NM_198503.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:36768620 G>A maps to NM_001031836.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr8:110980378 G>A maps to NM_014379.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr9:2718995 C>T maps to NM_133497.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr18:24128245 C>T maps to NM_001142730.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr12:109894045 G>C maps to NM_031954.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7256425 G>A maps to NM_001002914.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:77734211 C>A maps to NM_023930.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr22:37455444 C>T maps to ENST00000403888 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67325216 G>A maps to NM_001100915.1 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2752451 G>A maps to NM_018992.3 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr4:44449754 C>T maps to NM_198353.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:108350117 T>C maps to NM_153705.4 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:18212816 C>T maps to ENST00000388870 G656G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr11:66985326 G>A maps to NM_012308.2 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:121880537 G>A maps to ENST00000377071 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:121947468 G>A maps to ENST00000377071 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:86716754 G>A maps to NM_001146688.1 T1182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr5:137727793 G>T maps to NM_016604.3 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:137717275 C>T maps to NM_016604.3 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:5047488 C>T maps to NM_015015.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:5135489 G>A maps to NM_015015.2 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr19:5039896 C>T maps to NM_015015.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr19:5041159 G>A maps to NM_015015.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:404915 C>T maps to NM_001042603.1 V1426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr12:416933 T>A maps to NM_001042603.1 K1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr24:21871502 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr24:21868431 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr24:21883101 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr23:44938411 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr23:44969494 G>A did not map to a codon.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr23:44942768 A>T did not map to a codon.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr23:44938584 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:44929287 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:44937656 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr23:44949154 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr23:44945221 A>G did not map to a codon.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr23:44894230 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr23:44949993 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:7756413 C>T maps to NM_001080424.1 D1569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:55956220 G>A maps to NM_002253.2 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:55955036 G>A maps to NM_002253.2 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:142643377 G>A maps to NM_000420.2 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27315232 C>T maps to NM_006488.2 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:19559588 C>T maps to NM_015047.1 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr17:26951277 G>A maps to NM_014680.2 N1575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:141316894 C>T maps to NM_014773.3 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:73482397 G>A maps to ENST00000375248 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:42832598 C>T maps to NM_015349.1 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr14:105349540 G>A maps to ENST00000453495 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr6:24564489 G>A maps to NM_014809.3 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr6:24601302 G>T maps to NM_014809.3 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:35916051 C>T maps to NM_024874.4 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:34791437 C>T maps to NM_014686.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:34818984 C>T maps to NM_014686.3 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr9:114199252 A>G maps to NM_001080398.1 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr14:35592591 T>C maps to NM_014672.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr20:36640364 G>A maps to NM_014657.1 C618C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr7:4824596 C>T maps to ENST00000450194 A994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr1:43912678 G>A maps to NM_015284.2 V2143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr1:43913221 T>A maps to NM_015284.2 L2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43896377 G>A maps to NM_015284.2 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43896660 C>T maps to NM_015284.2 R707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43903310 G>A maps to NM_015284.2 A1213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43908201 A>G maps to NM_015284.2 R1789R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43908865 G>A maps to NM_015284.2 E1910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:47144279 G>A maps to NM_014774.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr1:3662337 C>T did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr16:85111073 G>A maps to NM_014732.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:85101006 G>T did not map to a codon.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:27782956 G>A maps to NM_015202.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:27585274 G>T maps to NM_015202.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:27689213 C>T maps to NM_015202.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:27784465 C>T maps to NM_015202.2 Y1415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr13:42273389 A>C maps to NM_015058.1 T1127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB20-01A-12D-A41K-08 chr13:42249394 G>C maps to NM_015058.1 V1455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr13:42259306 G>A maps to NM_015058.1 F1401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:42273242 A>G maps to NM_015058.1 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:42144706 G>A maps to NM_015058.1 R1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr14:58896078 A>G did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:138378218 C>T maps to NM_014811.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr9:138379679 G>A maps to NM_014811.3 G1108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr11:46690390 C>T maps to NM_001142673.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:6503778 C>T did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:39877440 G>T maps to NM_015038.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:96988478 C>T maps to NM_015323.4 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr18:8824762 G>A maps to ENST00000456698 E1404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:8825584 G>A maps to ENST00000456698 S1678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr14:55844785 A>G maps to NM_014924.3 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr14:55848899 T>A maps to NM_014924.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19451658 C>T maps to NM_015329.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67210860 C>T maps to NM_001040715.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr1:155896892 A>C did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr1:155887433 A>T maps to NM_014949.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OF-01A-11D-A41K-08 chr4:154544235 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:154517483 C>T maps to NM_001131007.1 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:5462083 G>A maps to NM_015325.1 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:5473843 G>A maps to NM_015325.1 T2132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr5:5462221 A>G maps to NM_015325.1 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:84884583 C>T maps to NM_014895.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:29488974 T>C did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr15:79748638 C>G maps to NM_015206.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:79749052 C>T maps to NM_015206.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:79750156 C>T maps to NM_015206.2 C556C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:123192754 G>A maps to NM_015312.3 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr4:123202795 A>G maps to NM_015312.3 P2968P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr4:123237981 A>G maps to NM_015312.3 E3545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:123227141 T>C maps to NM_015312.3 A3261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr23:118238970 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:118221658 A>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr4:57182746 C>T maps to NM_020722.1 Q1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr10:24669919 T>C maps to NM_019590.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:138655388 C>T maps to NM_020340.4 G1802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:128712141 C>T maps to NM_020741.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:44145008 C>A maps to NM_015443.3 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr10:72291080 G>A maps to NM_014431.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:86541552 C>T maps to NM_001142749.2 S668S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr14:94004550 G>T maps to ENST00000393153 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr14:94004513 G>A maps to ENST00000393153 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr14:94088366 G>A maps to ENST00000393153 P1618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:95502187 A>G maps to NM_015496.3 L1755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr8:95507177 G>C maps to NM_015496.3 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:95522014 G>A maps to NM_015496.3 F1260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:95539162 G>A maps to NM_015496.3 Q437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr4:186111651 C>T maps to NM_020827.1 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr4:186085309 G>A maps to NM_020827.1 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:186097205 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:5743013 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:5769249 C>T maps to ENST00000414202 R1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:30315488 C>T maps to NM_020848.2 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:59898498 C>T maps to NM_020854.3 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:59949645 C>T maps to NM_020854.3 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:226447104 G>A maps to NM_020864.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr2:226447086 G>T maps to NM_020864.1 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:33237578 G>A maps to NM_020888.2 A933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr9:100071829 G>A maps to ENST00000375206 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:100082479 G>A maps to ENST00000375206 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:1348987 A>G maps to NM_020894.2 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr4:1377681 C>T maps to NM_020894.2 Q664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr19:7682253 T>C maps to NM_001080429.2 P1112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:7677625 G>A maps to NM_001080429.2 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr6:56918133 A>G maps to NM_020931.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr6:56917923 A>G maps to NM_020931.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:56915636 C>T maps to NM_020931.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:118738783 G>A maps to NM_001127211.1 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:84514161 C>T maps to NM_020947.3 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr1:180885313 A>G maps to NM_020950.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:180905306 G>A maps to NM_020950.1 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr18:43438029 G>A maps to NM_020964.2 S2410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:44681531 G>A maps to NM_001099294.1 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18375973 G>A maps to NM_001145304.1 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr13:45594564 T>A did not map to a codon.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr20:36855561 G>A maps to NM_001029864.1 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:233518096 C>G maps to NM_032435.2 L917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:233482356 C>T maps to NM_032435.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr8:22472958 G>A maps to NM_021174.5 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22465542 C>T maps to NM_021174.5 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr9:139701516 C>A maps to NM_001039374.4 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr23:73963817 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:73965442 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr9:5920337 A>T maps to NM_001017969.2 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr9:5919990 G>C maps to NM_001017969.2 S2002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr9:6007387 C>A maps to NM_001017969.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:5988466 A>G maps to NM_001017969.2 C224C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr2:8940604 G>A maps to NM_020738.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:116858373 C>A maps to ENST00000259410 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:17800326 G>A maps to NM_022113.4 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr6:17826028 C>A maps to NM_022113.4 E586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr1:200587122 C>T maps to NM_014875.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr20:16360551 C>A maps to NM_024704.4 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr20:16409610 C>T maps to NM_024704.4 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:16360534 G>A maps to NM_024704.4 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr20:16360453 G>A maps to NM_024704.4 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr20:16485058 A>G maps to NM_024704.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:16359568 G>A maps to NM_024704.4 G1026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr20:16354923 G>A maps to NM_024704.4 L1110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr1:21031225 G>A maps to NM_020816.2 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:21040006 C>G maps to NM_020816.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:20991142 G>A maps to NM_020816.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:21009256 G>A maps to NM_020816.2 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:28058050 A>G maps to NM_031217.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr17:72340363 C>A maps to NM_153209.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:72347025 G>A maps to NM_153209.3 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr2:241725858 G>A maps to ENST00000373308 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr2:241689897 G>A maps to ENST00000373308 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:10292481 C>T maps to ENST00000377086 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr1:10380117 G>A maps to ENST00000377086 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:137520548 G>A maps to NM_005733.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr10:91512348 C>T maps to ENST00000416354 C1446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:39711939 A>G maps to ENST00000395670 R1281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:39760172 G>A maps to ENST00000395670 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr12:39760855 G>A maps to ENST00000395670 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:200972743 C>T maps to NM_017596.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr16:29816581 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr9:34257663 A>T maps to NM_194313.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:245849236 C>A maps to NM_018012.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr1:245850130 G>A maps to NM_018012.3 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:245852062 C>A maps to NM_018012.3 G1926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:51901668 C>T maps to NM_032559.4 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:51901788 G>A maps to NM_032559.4 Q465Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:45232617 C>T maps to NM_006845.3 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:132056316 C>T maps to ENST00000403231 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30904101 C>T maps to NM_004798.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:30897747 C>G maps to NM_004798.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr2:26203358 C>T maps to NM_002254.6 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr12:57962798 C>T maps to NM_004984.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:57957250 C>T maps to NM_004984.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr12:57957898 G>A maps to NM_004984.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr12:57972037 C>T maps to NM_004984.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr12:57963896 G>A maps to NM_004984.2 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr10:32337437 T>C maps to NM_004521.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:32329371 T>C maps to NM_004521.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:149853787 C>T maps to NM_004522.1 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr6:39507800 G>A maps to NM_145027.4 S541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr1:169953738 T>C maps to NM_014970.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr1:169952442 G>A maps to NM_014970.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:33377449 C>T maps to NM_002263.3 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr8:145697576 G>A maps to NM_145754.2 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:57794984 G>A maps to NM_005550.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:57798060 C>T maps to NM_005550.3 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:55294986 C>T maps to ENST00000291633 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:55341681 G>A maps to NM_013289.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr19:55340906 C>T maps to NM_013289.2 C364C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:158064570 C>T maps to ENST00000368173 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr1:158064804 G>A maps to ENST00000368173 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr4:55603398 C>T maps to NM_000222.2 Q919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr13:33635171 C>A maps to NM_004795.3 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr13:33628319 T>A maps to NM_004795.3 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr4:39448817 C>T maps to NM_175737.3 N824N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:104139524 G>A did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr11:66026226 G>T maps to NM_022822.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66031139 C>T maps to NM_022822.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr8:103664290 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:74269698 G>A maps to NM_007249.4 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:126071360 C>T maps to NM_014079.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr2:207988819 C>T maps to NM_003709.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr16:87788844 G>T maps to NM_017566.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:87743135 G>A maps to NM_017566.3 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr1:18809301 G>C maps to NM_152375.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:50987890 G>A maps to NM_138433.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50987554 G>A maps to NM_138433.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39998227 A>G maps to NM_152467.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:202880298 G>A maps to NM_021633.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr23:117053578 G>C did not map to a codon.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr23:117033091 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr23:24007024 A>G did not map to a codon.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr23:24006923 A>G did not map to a codon.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:47364055 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:166234519 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr4:166218864 A>G maps to NM_001161521.1 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:170592129 G>A maps to NM_144711.5 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:183368575 C>T maps to NM_017644.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:86312336 G>A maps to NM_022480.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18779106 G>A maps to NM_018316.1 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:136963995 C>T maps to NM_017415.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:136969759 G>A maps to NM_017415.2 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:97587106 C>T maps to NM_052904.3 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr23:86888855 G>A did not map to a codon.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr23:86887269 T>C did not map to a codon.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr23:86919797 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:23205408 C>T maps to NM_001031710.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:88085049 C>T maps to NM_020803.3 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:21334741 G>A maps to NM_018847.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr19:51534118 G>T maps to NM_019598.2 C172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr19:51582741 G>A maps to NM_022046.4 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr19:51330398 C>G maps to NM_017509.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:51329882 G>T maps to NM_017509.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr19:51361551 C>G maps to NM_001648.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:51412614 C>T maps to NM_004917.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr19:51412614 C>T maps to NM_004917.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr19:51451964 A>G maps to NM_012427.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:51453322 G>A maps to NM_012427.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:51451970 G>A maps to NM_012427.4 C217C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:51466702 G>A maps to NM_001012964.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr19:51480875 G>A maps to NM_005046.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:51507094 C>T maps to NM_012315.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:51509867 G>A maps to NM_012315.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:47014925 G>A maps to ENST00000481882 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:47016749 G>A maps to ENST00000481882 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr10:135024979 C>T maps to ENST00000368572 C1323C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:122160928 G>A maps to NM_002264.3 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr3:122180093 G>A maps to NM_002264.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:117043315 C>T maps to NM_002269.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr1:152732099 G>A maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:149416749 G>A maps to NM_032534.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:8273383 G>A maps to NM_213597.2 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr19:10670557 C>T maps to NM_023008.3 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr7:91870305 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:38978720 G>A maps to NM_000421.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39739361 C>T maps to NM_000526.4 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr17:39672160 G>A maps to NM_002275.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr17:39767649 G>A maps to NM_005557.3 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39034434 A>G maps to NM_019010.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:38905555 G>C maps to NM_181534.3 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr17:38907295 G>A maps to NM_181534.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr17:38938514 G>A maps to NM_181537.3 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr17:38933945 A>G maps to NM_181537.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr17:38935996 G>A maps to NM_181537.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:38950184 G>A maps to NM_181535.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:53185102 C>T maps to ENST00000309505 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr17:39502451 A>G maps to NM_004138.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr17:39520186 G>A maps to ENST00000394004 C373C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:39521646 C>T maps to ENST00000394004 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr17:39635634 C>T maps to NM_002280.4 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39635745 C>T maps to NM_002280.4 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr17:39595065 A>G maps to NM_006771.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr12:53201524 G>A maps to NM_002272.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr12:53202550 G>A maps to NM_002272.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39135120 G>A maps to NM_182497.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:52882149 G>A maps to NM_005554.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr12:52884406 A>G maps to NM_005554.3 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr12:52820635 C>A did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr12:53242525 C>A maps to NM_173352.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr12:53217007 G>A maps to NM_175834.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:52681013 G>A maps to NM_002281.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:52681896 G>T maps to NM_002281.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:52700019 C>T maps to NM_002284.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:52699572 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr17:39190953 G>A maps to NM_030966.1 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr17:39190674 G>T maps to NM_030966.1 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr17:39183230 A>G maps to NM_031957.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr21:45959619 C>T maps to NM_198691.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr21:46021150 G>A maps to ENST00000380102 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr21:46047204 G>A maps to NM_198690.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:31864119 G>A maps to ENST00000433652 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:31933434 C>T maps to NM_181614.1 W58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:32410756 G>A maps to NM_001099219.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr21:32127654 G>T maps to NM_181619.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr21:31692134 G>A maps to NM_203405.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr17:39254036 G>A maps to NM_031960.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:39261948 T>C maps to NM_001146041.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr17:39261741 C>T maps to NM_001146041.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr11:1606149 G>A maps to NM_001005922.1 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:1606353 G>A maps to NM_001005922.1 C42C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:71293805 A>T maps to ENST00000376535 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr11:1629258 C>T maps to ENST00000359229 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr11:71238579 C>T maps to NM_001012503.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr11:71259903 C>T maps to ENST00000422553 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr17:39383025 C>T maps to NM_031961.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr17:39388890 C>T maps to NM_031962.2 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr17:39389178 C>A maps to NM_031962.2 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:39411906 C>T maps to ENST00000431129 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:25932770 G>A maps to ENST00000268763 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr12:118298122 G>A maps to ENST00000339824 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:118198838 G>A maps to ENST00000339824 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr12:118199015 C>T maps to ENST00000339824 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:118199030 C>T maps to ENST00000339824 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:143790836 C>T maps to NM_003937.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr23:153135592 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr23:153135087 T>C did not map to a codon.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr23:153137809 C>T did not map to a codon.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr23:153136388 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:153132318 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153137793 C>T did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:153130076 G>C did not map to a codon.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr23:153137797 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr23:153130846 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:62672629 A>G maps to NM_019079.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:50750646 G>A maps to NM_024884.2 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:42161555 T>C maps to NM_032107.4 Y454Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr20:42168797 G>A maps to NM_032107.4 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr6:130387568 C>T maps to NM_032438.2 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:130376383 G>A maps to NM_032438.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:108798483 C>T maps to NM_145315.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr1:201356119 G>A maps to NM_005558.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr19:54872559 C>T maps to NM_002287.3 W109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr18:6943332 C>A maps to NM_005559.2 V2971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr18:7034682 C>A maps to NM_005559.2 G616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:6959467 G>A maps to NM_005559.2 I2550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:7023301 G>A maps to NM_005559.2 N854N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:129601259 C>T maps to NM_000426.3 C835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr6:129824262 C>T maps to NM_000426.3 T2795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr6:129371233 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:129837345 C>T maps to NM_000426.3 Q3075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr18:21426326 C>T maps to ENST00000416669 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr18:21492719 C>T maps to ENST00000416669 R2404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr18:21501018 G>T did not map to a codon.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr18:21441708 G>T maps to ENST00000416669 E1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr18:21330979 T>C maps to ENST00000416669 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:21402283 C>T maps to ENST00000416669 Y793Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:21501507 C>T maps to ENST00000416669 S2714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr18:21513896 C>T maps to ENST00000416669 Q2956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr6:112430675 G>A maps to NM_001105206.1 S1812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr20:60884511 G>C maps to NM_005560.3 P3656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:107592540 C>T maps to NM_002291.2 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr7:107703338 C>T maps to NM_007356.2 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr9:133928257 C>T maps to ENST00000355048 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr3:182853619 C>T maps to NM_014398.3 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr2:211336686 C>T maps to NM_001136575.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr4:129121698 C>T maps to NM_018078.2 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:50824351 C>T maps to ENST00000429001 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr17:37074902 G>T maps to NM_006148.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:37074901 C>T maps to NM_006148.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr2:169417808 G>A maps to ENST00000392687 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B2-01A-12D-A32B-08 chr16:28997052 C>G maps to NM_014387.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr13:21557699 G>A maps to NM_014572.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:21562220 G>A maps to NM_014572.2 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:36974955 C>T maps to NM_004139.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:68118588 C>T maps to ENST00000380035 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:152777720 G>A maps to NM_178351.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr1:152777633 G>A maps to NM_178351.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr1:152760035 T>C maps to ENST00000417924 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:152659384 A>G maps to NM_014357.4 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr1:152538500 G>A maps to NM_178435.2 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr1:32745332 G>A maps to ENST00000373562 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr15:43620820 A>G maps to NM_014793.4 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr15:43621412 G>A maps to NM_014793.4 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr15:43621658 G>C maps to NM_014793.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:139847393 G>A maps to NM_178536.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr9:139651557 C>T maps to ENST00000371689 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr9:138557737 G>A maps to ENST00000277526 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr13:46701743 T>C maps to NM_002298.4 K622K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr2:136566178 G>A maps to NM_002299.2 N1246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr2:136558281 G>A maps to NM_002299.2 R1587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr2:136570300 G>A maps to NM_002299.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:136570439 G>A maps to NM_002299.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr15:66850144 G>A maps to NM_207338.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:103867966 G>A maps to NM_001113407.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr4:16590332 A>G maps to NM_001290.3 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr10:88447003 C>T maps to NM_001171610.1 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:88476312 T>C maps to NM_001171610.1 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:11233931 A>T maps to NM_000527.4 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:11224017 C>T maps to NM_000527.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:11221442 C>T maps to NM_000527.4 C352C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr22:44892838 G>A maps to NM_032287.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:44892884 C>T maps to NM_032287.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:54663421 C>T maps to NM_024316.1 L4L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr19:54965661 G>A maps to ENST00000431846 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:127894590 C>T maps to NM_000230.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:65895625 C>T maps to NM_017526.4 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr4:1821091 C>T maps to NM_012318.2 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr4:1834578 C>T maps to NM_012318.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:1818467 G>A maps to NM_012318.2 N639N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:2564898 G>A maps to NM_001040167.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr7:2566510 C>G maps to NM_001040167.1 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:40199919 T>C maps to NM_203471.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39299545 G>A maps to NM_006149.3 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39303129 G>A maps to NM_006149.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr19:39281376 C>G maps to NM_001042507.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr10:95518092 C>G maps to NM_005097.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr4:25005537 G>A maps to NM_018176.3 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:22006440 G>A maps to NM_139278.2 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:27395186 C>T maps to NM_018490.2 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr12:71978096 C>A maps to NM_003667.2 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:202245637 C>T maps to NM_001017403.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr1:202205106 G>A maps to NM_001017403.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr6:63990990 G>A maps to NM_016571.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr6:63990359 G>A maps to NM_016571.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr6:63990018 G>A maps to NM_016571.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr6:63991020 G>A maps to NM_016571.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:206782804 C>T maps to NM_006893.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr2:48915654 A>T maps to NM_000233.3 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr5:77784959 G>T maps to NM_005779.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:180235655 G>C maps to NM_033343.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr1:197898208 C>T maps to NM_020204.2 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:108861450 C>T maps to NM_001098268.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:55106787 G>A maps to NM_006863.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:55086795 G>A maps to NM_001130917.1 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr19:54802056 C>T maps to ENST00000251375 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr19:54745450 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr19:55148262 T>G maps to ENST00000427581 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr19:55148289 A>T maps to ENST00000427581 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:54778647 G>A maps to ENST00000391747 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr19:54721087 G>T maps to NM_001081450.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:54760065 G>T maps to NM_001081442.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr4:41621367 G>A maps to NM_014988.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:41621298 G>A maps to NM_014988.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:41608015 C>T maps to NM_014988.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr17:61776289 G>A maps to NM_030576.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61775912 C>T maps to NM_030576.3 *128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:73511050 C>T maps to NM_002314.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:109292447 C>T maps to NM_001193484.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:128399722 C>A maps to NM_017980.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:77907624 G>A maps to NM_032808.5 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr1:151773575 C>T maps to NM_001004432.2 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:58830635 C>T maps to NM_000236.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:58834093 C>T maps to NM_000236.2 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:42910405 G>A maps to NM_005357.2 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr21:15561723 G>T maps to NM_198996.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:18137335 C>T maps to NM_004140.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18137431 G>A maps to NM_004140.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18139974 G>A maps to NM_004140.3 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18141891 C>T maps to NM_004140.3 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:73559542 C>T maps to NM_001031803.1 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr15:75114225 C>T maps to NM_021819.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr2:97377672 G>A maps to NM_001142292.1 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr3:8578933 C>T maps to NM_014583.2 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:197707372 C>T maps to NM_001136049.2 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:197762891 C>T maps to NM_001136049.2 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:33886236 G>A maps to NM_005574.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr13:76379698 G>A maps to ENST00000357063 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr3:69168011 C>A maps to NM_198271.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:129458220 C>T maps to NM_001174147.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:100170609 G>A maps to ENST00000489752 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr5:96362363 A>T maps to NM_005575.2 K923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:96315334 C>T maps to NM_005575.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr4:54440052 G>A maps to NM_001126328.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr16:20855294 C>T maps to NM_030941.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:5707725 G>A maps to NM_004793.2 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:12594256 T>C maps to NM_152271.3 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr15:74219534 G>C maps to NM_005576.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:23225612 G>A maps to NM_002318.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr2:74762801 G>A maps to NM_032603.2 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr6:161020596 A>G maps to NM_005577.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:160969575 C>A maps to NM_005577.2 E1697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr9:113704387 G>A maps to NM_057159.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr23:78010845 T>C did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:1470988 G>A maps to NM_024830.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr1:211923270 G>A maps to NM_014873.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:14267882 G>A maps to NM_001008701.2 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:62599225 C>T maps to ENST00000506720 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr4:62903459 G>A maps to ENST00000506720 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:62758467 G>A maps to ENST00000506720 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr4:62903475 C>T maps to ENST00000506720 R1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr4:62812713 G>A maps to ENST00000506720 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:11919741 C>T maps to ENST00000396099 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr2:11955223 A>T maps to ENST00000396099 K760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr17:56345180 C>T maps to NM_006151.2 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr3:188327154 G>T maps to NM_005578.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr19:11472139 C>T maps to NM_001170635.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:11470257 G>A maps to NM_022737.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:99772184 G>A maps to NM_014839.4 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr1:99422182 G>A maps to NM_001037317.1 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:99470128 C>T maps to NM_001037317.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:151682933 C>A did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:47269053 G>T maps to NM_001164211.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:47286658 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:47315856 C>T maps to NM_001164211.1 L722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr7:100179756 G>A maps to NM_002319.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:803449 G>A maps to NM_145886.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:800377 G>A maps to NM_145886.3 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr19:39804776 C>T maps to NM_020862.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr6:40359849 C>T maps to NM_020737.1 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:36431058 G>A maps to NM_024509.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr14:42356736 G>A maps to NM_152447.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr19:4538287 C>T maps to NM_052972.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr3:66502032 T>C maps to NM_015541.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:66431253 G>A maps to NM_015541.2 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:113636958 A>T did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr12:59283854 G>A maps to NM_153377.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr10:85992630 C>T maps to NM_015613.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr10:85981738 G>A maps to NM_001017924.2 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:57574173 C>T maps to NM_002332.2 I1766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:57539194 C>T maps to NM_002332.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:57579326 C>T maps to NM_002332.2 C2159C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr2:141739813 G>A maps to NM_018557.2 C934C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:141356217 G>A maps to NM_018557.2 Y2392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:141609266 C>T maps to NM_018557.2 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr2:141665494 G>A maps to NM_018557.2 C1157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr2:141253251 G>A maps to NM_018557.2 C2972C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr2:141108608 T>A did not map to a codon.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr2:141245238 G>A maps to NM_018557.2 R3064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:170068628 G>A maps to NM_004525.2 C2043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:170136032 G>A maps to NM_004525.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:170048427 G>A maps to NM_004525.2 Y2982Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:170099967 C>T maps to NM_004525.2 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:46921855 G>A maps to ENST00000256991 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr11:46924427 T>G maps to ENST00000256991 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr12:12397550 G>T maps to NM_002336.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:53728130 G>A maps to NM_004631.3 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:44153049 T>C maps to NM_133259.3 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr12:70003940 G>A maps to NM_201550.2 N226N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:25472739 G>T maps to NM_017640.5 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:25600697 C>T maps to NM_017640.5 P1092P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:24524776 C>T maps to NM_138360.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr3:46586568 C>T maps to NM_024512.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:18507626 G>A maps to NM_145256.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr10:134158048 G>T maps to NM_030626.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr10:134165246 C>T maps to NM_030626.2 Q355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr10:134165158 G>A maps to NM_030626.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:7231882 C>T maps to NM_001105581.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr11:76371901 G>A maps to NM_001128922.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:44626191 C>T maps to NM_001006607.2 N1229N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:30349139 A>C maps to ENST00000327564 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr12:122669142 C>T maps to NM_001098519.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr15:71185231 T>G did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr19:51021544 A>G maps to NM_001080457.1 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DQ-01A-11D-A377-08 chr19:51051831 C>T maps to NM_001080457.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr11:40137467 G>A maps to NM_020929.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr11:40136648 C>T maps to NM_020929.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr11:56949993 C>T maps to NM_001005210.2 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:42839683 C>A maps to NM_153260.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:150034681 G>A maps to NM_023942.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:150034639 C>A maps to NM_023942.2 C230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:52861921 G>A maps to NM_001024611.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr4:52860764 G>C maps to NM_001024611.1 S808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:52861264 G>A maps to NM_001024611.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr8:67922952 C>G maps to ENST00000421742 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:70502286 T>C maps to NM_020794.2 H718H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr1:70504093 C>T maps to NM_020794.2 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr1:70484493 T>C maps to NM_020794.2 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr1:90048353 C>T maps to NM_015350.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr1:90178509 C>T maps to NM_032270.4 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:90180447 C>T maps to NM_032270.4 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:90179784 C>T maps to NM_032270.4 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:90400075 C>T maps to NM_001134479.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:90399035 C>T maps to NM_001134479.1 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr19:7964265 A>C maps to NM_025061.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr2:238668783 A>G maps to NM_001137552.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:37125218 A>G maps to NM_006309.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr12:85518198 G>A maps to NM_001079910.1 K1303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr12:85450802 C>T maps to NM_001079910.1 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:85547498 C>T maps to NM_001079910.1 L1534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:74575076 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:74648335 C>T maps to NM_001105659.1 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A722-01A-12D-A364-08 chr3:169539972 G>A maps to NM_001080460.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr15:101592009 C>G maps to NM_024652.3 P1178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr15:101595337 G>A maps to NM_024652.3 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr12:40689227 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr3:3887995 G>T maps to NM_020873.5 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:204589108 G>A maps to NM_201630.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:110763517 C>T maps to NM_018334.4 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:62455620 G>A maps to NM_203422.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:80530233 C>A maps to NM_178839.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:80530542 C>T maps to NM_178839.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr2:80529774 C>T maps to NM_178839.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:138209843 G>A maps to NM_015564.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:68687897 C>T maps to NM_178011.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr2:76975913 G>A maps to NM_001134745.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr2:77745758 G>A maps to NM_001134745.1 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr12:1943628 G>A maps to NM_001163926.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:60701436 C>T maps to NM_144703.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr11:1904666 C>T maps to ENST00000381758 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:35753474 C>T maps to NM_205834.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr21:47615596 G>A maps to NM_002340.5 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr12:21207528 C>T maps to ENST00000381541 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:33172886 T>C did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr11:65315006 G>A maps to NM_001130144.2 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr19:41117232 G>T maps to ENST00000308370 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41125315 C>T maps to ENST00000308370 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr19:41132931 G>A maps to ENST00000308370 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr19:41135317 G>T maps to ENST00000308370 E1579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr15:41804905 G>A maps to NM_002344.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A722-01A-12D-A364-08 chr17:48819019 C>A maps to ENST00000393227 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:91502030 A>G maps to NM_002345.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr1:23418231 A>G maps to NM_001142546.1 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:23417972 G>A maps to NM_001142546.1 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr23:114541232 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr8:143784548 C>T maps to ENST00000292430 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr8:143781998 C>T maps to ENST00000292430 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:160710868 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160688256 C>T maps to NM_001198759.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160710868 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:160706544 C>T maps to NM_001198759.1 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr2:160665082 C>A did not map to a codon.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:160771694 G>A maps to NM_001033667.1 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:160784291 C>G maps to ENST00000263285 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:4281392 A>T maps to NM_017816.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:4285406 A>G maps to NM_017816.2 H21H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr19:13211895 T>G maps to NM_005583.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:13211555 G>A maps to NM_005583.4 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr8:56860228 C>A maps to NM_002350.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:56863269 C>T maps to NM_002350.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:43965685 G>A maps to NM_014400.2 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:150325225 C>A maps to NM_194317.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr1:219347259 C>T maps to NM_138794.3 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:151137674 C>T maps to NM_212551.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr15:100269695 G>A maps to NM_152449.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:235950606 A>G maps to NM_000081.2 N1585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr1:235944226 G>A maps to NM_000081.2 R1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:235944226 G>A maps to NM_000081.2 R1718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr22:21349316 T>G did not map to a codon.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr8:20110913 C>T maps to NM_021020.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:20107640 C>T maps to NM_021020.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr8:20110544 C>T maps to NM_021020.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:9095067 C>A maps to NM_002355.2 G219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr13:36050005 G>A maps to NM_005584.4 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:39798823 A>G maps to ENST00000289893 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:39747938 C>T maps to ENST00000361689 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr1:39783025 A>G maps to ENST00000361689 K1248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr1:39798763 T>C maps to ENST00000289893 F608F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:39827168 C>T maps to ENST00000361689 F2135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:39927669 G>A maps to ENST00000361689 A5154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:2259031 C>T maps to NM_003550.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:47345220 G>C did not map to a codon.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:47296302 G>A maps to NM_003682.3 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:47308005 T>C maps to NM_003682.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr19:35793405 G>A maps to NM_002361.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:35786681 G>A maps to NM_002361.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr19:35790571 C>T maps to NM_002361.3 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:152482196 C>T did not map to a codon.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr23:151303816 G>A did not map to a codon.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr23:151303839 G>T did not map to a codon.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr23:151303215 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr23:151303918 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr23:148798035 T>A did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr23:151900632 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr23:151092294 A>G did not map to a codon.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr23:151093030 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr23:151092402 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:151092277 C>A did not map to a codon.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr23:151869831 C>T did not map to a codon.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr23:151869727 G>A did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr23:151869993 A>C did not map to a codon.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr23:151869831 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:151869696 G>A did not map to a codon.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr23:151869897 G>T did not map to a codon.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr23:151870215 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:27839512 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:30237394 A>G did not map to a codon.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr23:30260825 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr23:26212430 G>T did not map to a codon.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr23:26212571 G>A did not map to a codon.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr23:26212778 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr23:26212006 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr23:140996359 G>A did not map to a codon.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr23:140995224 C>A did not map to a codon.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr23:140995015 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr23:140994959 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:140994456 A>C did not map to a codon.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr23:140996225 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:141291202 G>A did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr23:140985037 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr23:140983189 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:51639837 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:75649355 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:75004664 C>T did not map to a codon.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr15:23889169 G>A maps to NM_019066.4 H1240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:23889637 G>A maps to NM_019066.4 N1084N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr7:77764434 C>A maps to NM_012301.3 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr7:77973248 G>T maps to NM_012301.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:77764473 G>T maps to NM_012301.3 R965R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:114201720 C>T maps to NM_001142782.1 G883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:77150898 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:120233894 G>A maps to ENST00000276681 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139751934 C>T maps to ENST00000392881 C824C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr9:139748448 C>T maps to ENST00000392881 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr5:179193304 C>T maps to NM_014757.4 Q432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr4:141074097 G>T maps to ENST00000509479 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr23:149671651 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr23:149639650 A>G did not map to a codon.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr23:149642056 G>A did not map to a codon.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:149639451 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr6:119510997 G>A maps to NM_005907.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:12767771 C>T maps to NM_000528.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75648506 G>A maps to NM_006715.2 H980H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:12483539 C>T maps to NM_018050.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr23:43571168 T>A did not map to a codon.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr23:43590979 G>A did not map to a codon.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr23:43652800 G>C did not map to a codon.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr23:43655004 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr15:43821218 G>A maps to ENST00000382031 P2754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr15:43815431 A>G maps to ENST00000382031 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr15:43821146 C>A maps to ENST00000382031 C2730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:43814555 G>A maps to ENST00000382031 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:43817298 C>T maps to ENST00000382031 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:43818077 G>A maps to ENST00000382031 K1707K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:71495574 G>A maps to NM_005909.3 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A8TL-01A-21D-A377-08 chr5:71492634 G>A maps to NM_005909.3 E1151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:17835964 T>G maps to NM_018174.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:17837218 C>T maps to NM_018174.4 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr2:210588328 T>A maps to NM_001039538.1 L396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:210560391 C>T maps to NM_002374.3 A1166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr2:210561045 C>T maps to NM_002374.3 D1384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:4110566 G>A maps to NM_030662.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr17:12032508 T>C maps to ENST00000415385 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67513025 C>T maps to NM_002758.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:67501928 C>T maps to NM_002758.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:56176630 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:56177975 G>A maps to NM_005921.1 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr19:40715126 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:40711064 C>T maps to NM_002446.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:65375264 G>A maps to NM_002419.3 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65366865 G>A maps to NM_002419.3 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr12:53878998 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:185169093 C>T maps to NM_004721.3 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr17:43345070 C>T maps to ENST00000344686 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:19389111 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:19482400 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr23:19413306 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:128065337 C>T maps to NM_006609.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61769175 C>T maps to NM_203351.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr6:136990478 C>A maps to NM_005923.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr6:136913364 G>T maps to NM_005923.3 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:27687251 G>A maps to NM_004672.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:71215543 A>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:71216680 C>T maps to NM_033141.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:71267461 G>A maps to NM_033141.2 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr3:47963255 G>A maps to ENST00000426837 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:47912425 T>C maps to ENST00000426837 K2057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr11:64559402 C>T maps to NM_004579.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64569093 C>A did not map to a codon.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr2:39517447 A>G maps to NM_003618.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:102505310 C>T maps to NM_145686.2 R1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:136683811 G>T maps to NM_001198609.1 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:36643581 C>T maps to NM_018067.3 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr23:20033398 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr23:20060692 A>G did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:135314291 G>T did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:135309467 T>A did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr23:135314094 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:55529373 C>A maps to NM_144578.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr16:1774641 C>T maps to NM_015133.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr9:128230299 G>A maps to NM_001006617.1 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:206858780 C>G maps to NM_032960.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42111442 G>T did not map to a codon.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr20:31427558 C>G maps to NM_012325.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr20:31424468 A>G maps to NM_012325.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr4:164534518 A>G maps to ENST00000514618 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:126250789 G>A maps to NM_178450.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr1:220791997 A>G maps to NM_018650.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:63671553 C>T maps to NM_001039469.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr14:103969416 G>A maps to ENST00000335102 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:71674558 G>T maps to NM_001017967.2 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr3:186954107 G>A maps to NM_139125.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr3:186978565 G>A maps to NM_139125.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr19:12978319 C>T maps to NM_014975.2 H724H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:12975904 C>T maps to NM_014975.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:12979923 C>T maps to NM_014975.2 R940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:46497979 C>T maps to NM_015112.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:46493408 A>T maps to NM_015112.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr19:18255925 C>T maps to NM_015016.1 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18254659 C>T maps to NM_015016.1 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:66460262 C>T maps to NM_001164664.1 A1752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:66461159 G>A maps to NM_001164664.1 A2051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr10:82034333 G>A maps to NM_000429.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr1:31189119 G>A maps to NM_002379.3 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:43926837 C>T maps to ENST00000372754 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:138643656 A>C maps to ENST00000394800 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr20:3843001 T>C maps to NM_020746.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr18:47801394 G>A maps to ENST00000424334 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr3:129155913 C>T maps to NM_003925.1 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:149247601 C>A maps to ENST00000404807 V1467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr10:54531227 C>T maps to NM_000242.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr23:131516261 C>A did not map to a codon.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr18:74702001 C>T maps to NM_001025101.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:84104351 G>A maps to NM_003791.2 N541N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr16:84089608 C>A did not map to a codon.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr16:84124505 A>T maps to NM_003791.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:84129222 C>T maps to NM_003791.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr18:13885199 G>A maps to NM_000529.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr20:54823919 G>T maps to ENST00000371389 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr18:13826201 C>T maps to NM_005913.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:103349893 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:103349172 C>A did not map to a codon.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr22:43529099 C>T maps to NM_173467.4 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:112384867 G>A maps to NM_001085377.1 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr3:182756831 G>T maps to NM_020166.3 Y453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr23:138678881 G>A did not map to a codon.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr13:113732743 G>A maps to NM_001112732.1 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:182941897 G>A maps to NM_015078.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr6:100390895 C>T maps to NM_032503.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:100390835 G>A maps to NM_032503.2 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr10:13213057 C>T maps to NM_182751.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:13230973 C>T maps to NM_182751.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr10:13240782 A>G maps to NM_182751.2 S739S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:127336183 G>A maps to NM_004526.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:127337955 C>T maps to NM_004526.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr6:52148177 T>C maps to ENST00000419835 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr2:136630396 C>A maps to NM_005915.4 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:136605707 G>T maps to NM_005915.4 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:99690697 G>A maps to NM_005916.3 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr20:5967930 C>T maps to NM_032485.4 R723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:7595239 G>A maps to NM_020533.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:85510884 G>A maps to NM_018298.9 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr1:85486890 C>T maps to NM_018298.9 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr15:95013612 G>A maps to NM_018349.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:47504409 T>C maps to NM_001113498.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr14:47600971 C>T maps to NM_001113498.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:75686749 G>A maps to NM_005918.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr6:90426385 G>A maps to NM_014611.1 D2242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:90422346 C>T maps to NM_014611.1 Q2459Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:90426430 G>A maps to NM_014611.1 S2227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr6:84140594 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:168834357 C>G maps to NM_004991.3 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153297981 A>G did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr23:70357095 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr23:70356861 A>C did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr23:70349254 G>C did not map to a codon.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr23:70348522 G>C did not map to a codon.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr23:70349257 C>T did not map to a codon.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr23:70349254 G>C did not map to a codon.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr23:70349255 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:151107923 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:151150561 G>A maps to NM_053002.4 V2136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:60140572 G>A maps to NM_005121.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OF-01A-11D-A41K-08 chr17:60112845 T>C maps to NM_005121.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:60028340 G>A maps to NM_005121.2 L2046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:116457670 C>T maps to NM_015335.4 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:116446660 C>A maps to NM_015335.4 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr12:116446366 T>C maps to NM_015335.4 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr23:40572272 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:40556411 C>T did not map to a codon.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr22:20937035 T>A did not map to a codon.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr22:20929419 C>G maps to NM_001003891.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr6:131908953 A>T maps to ENST00000403834 A1330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr17:38182485 A>T maps to NM_014815.3 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr17:38182575 A>C maps to NM_014815.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50338352 C>T maps to NM_030973.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr19:16688031 G>T maps to NM_004831.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:134889830 T>C maps to NM_004269.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr8:118533267 C>A maps to NM_080651.2 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156438738 A>G maps to NM_005920.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156444987 C>T maps to NM_005920.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:3306385 G>A maps to NM_000243.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr16:3304557 G>A maps to NM_000243.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MK-01A-11D-A364-08 chr16:3297231 C>T maps to NM_000243.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3306560 C>T maps to NM_000243.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:126771181 G>C did not map to a codon.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr5:126784894 C>T maps to NM_032446.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr15:66215181 G>A maps to NM_032445.2 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:3511908 G>A maps to ENST00000452816 C198C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr1:3428621 C>T maps to ENST00000452816 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:42855366 G>T did not map to a codon.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr9:123367896 T>C maps to ENST00000426959 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:37188834 G>A maps to NM_170675.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:37388507 G>A maps to NM_170675.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr7:100031159 C>T maps to NM_019606.5 R685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr2:112702568 C>A maps to NM_006343.2 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:81271610 A>G maps to NM_015154.1 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr15:90293434 A>C maps to NM_018670.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr15:90320475 G>A maps to NM_001039958.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr7:116399498 G>A maps to NM_001127500.1 P791P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr1:171761208 C>T maps to NM_015935.4 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr1:171756945 C>T maps to NM_015935.4 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr1:171761358 G>A maps to NM_015935.4 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr1:171753486 G>A maps to NM_015935.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:170677647 G>A maps to NM_014168.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156046388 C>T maps to NM_001093725.1 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:82336337 C>T maps to NM_032246.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:82336499 G>A maps to NM_032246.3 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:153433125 T>C maps to NM_005927.4 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:170913386 C>T maps to NM_021647.6 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr4:170912696 G>C maps to NM_021647.6 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr12:8804282 G>T maps to NM_003480.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:89453091 G>A maps to NM_005928.2 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr15:89442667 C>T maps to NM_005928.2 W374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:8749968 C>A maps to NM_004225.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:8747721 T>C maps to NM_004225.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr3:196742334 C>T maps to NM_005929.5 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:12058936 T>A did not map to a codon.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr1:12052705 G>A maps to NM_014874.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:37876260 G>A maps to NM_002405.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr11:119213426 C>T maps to NM_031433.2 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr17:74738071 C>T maps to NM_024311.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:103335661 G>A maps to NM_032718.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr15:41961929 G>T maps to ENST00000219905 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr15:42003249 C>G maps to ENST00000219905 Y929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42003159 G>A maps to ENST00000219905 K899K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:141754595 C>T maps to ENST00000475668 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:141752696 C>T maps to ENST00000475668 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:141765239 A>G maps to ENST00000475668 A1530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr7:141719105 C>T maps to ENST00000475668 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:50088159 C>A maps to NM_002408.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:39883621 C>A maps to NM_001098270.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:43280398 C>T maps to NM_153361.2 H293H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr5:43280300 T>C maps to NM_153361.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr10:131506293 C>A maps to NM_002412.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:222805660 G>C maps to NM_198551.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr1:222838750 A>T maps to NM_198551.2 G1838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:19348667 C>T maps to NM_020774.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:1562800 G>A maps to NM_080875.2 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr11:12265583 C>G maps to NM_014632.2 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38318134 G>A maps to NM_033386.2 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr7:1477838 G>A maps to NM_182924.3 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr23:10417582 T>C did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr23:38664271 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:107159357 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:67447510 C>T maps to NM_001077700.2 R427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:7645693 T>C maps to NM_019005.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:129900971 G>C maps to NM_002417.4 P3044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr10:129899950 G>A maps to NM_002417.4 R3092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr10:129905900 C>T maps to NM_002417.4 Q1401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:129910062 A>T maps to NM_002417.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:129901244 T>C maps to NM_002417.4 G2953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr22:40816927 G>C maps to NM_020831.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:40820290 C>T maps to NM_020831.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr7:131172447 T>G maps to NM_013255.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr19:2041131 G>A maps to NM_199054.2 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2043566 C>T maps to NM_199054.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:27964289 G>A maps to NM_173576.2 N309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr22:50500056 G>A maps to NM_015166.3 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:6858043 G>A maps to NM_005439.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr3:37067363 G>A maps to NM_000249.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:74708870 C>T maps to NM_152649.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:118343970 T>C maps to NM_001197104.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118368688 G>A maps to NM_001197104.1 W1901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118390415 C>T maps to NM_001197104.1 R3744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:49443871 C>A maps to NM_003482.3 E1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:49430958 G>A maps to NM_003482.3 Q3394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:49445332 C>T maps to NM_003482.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr12:49416432 G>C maps to NM_003482.3 Y5426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr12:49434306 G>A maps to NM_003482.3 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:151932987 T>A maps to ENST00000355193 R895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:151879330 G>A maps to ENST00000355193 Q1872*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr7:151873584 G>A maps to ENST00000355193 Q2985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr7:151970808 A>T maps to ENST00000355193 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr7:151855998 C>T maps to ENST00000355193 E3873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr7:151878019 G>A maps to ENST00000355193 Q2309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr7:151877200 A>C maps to ENST00000355193 L2387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:151836803 G>A maps to ENST00000355193 R4863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:151874058 G>A maps to ENST00000355193 L2827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:151879307 C>T maps to ENST00000355193 P1879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:151917818 G>A maps to ENST00000355193 D1167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:151921188 G>A maps to ENST00000355193 C1078C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr7:151860194 T>C maps to ENST00000355193 Q3489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:36229229 C>T maps to NM_014727.1 D2640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:36215969 C>T maps to NM_014727.1 R1170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:36219725 G>A maps to NM_014727.1 A1541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:104751017 C>T maps to NM_182931.2 G1313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:6216423 C>T maps to NM_005934.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:6222296 C>T maps to NM_005934.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr9:20414336 G>A maps to NM_004529.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr9:20414351 G>A maps to NM_004529.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr9:20414315 G>A maps to NM_004529.2 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:168297652 G>T did not map to a codon.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr6:168352504 C>T maps to ENST00000400822 Q1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:49795156 G>A maps to NM_001507.1 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:238419297 C>T maps to NM_024101.5 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:238434377 C>T maps to NM_024101.5 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr3:154861329 A>G maps to NM_007289.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr1:2537011 G>A maps to NM_033467.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:2535385 G>A maps to NM_033467.3 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr8:89128876 C>T maps to NM_005941.4 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr8:89128917 T>G maps to NM_005941.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr8:89068387 G>A maps to NM_005941.4 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr12:132322840 G>A maps to NM_016155.4 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3100100 C>T maps to NM_022468.4 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5011026 G>A maps to NM_021801.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr11:102710882 A>G maps to NM_002422.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr20:44641090 G>A maps to NM_004994.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:90816529 T>C maps to NM_007351.2 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr10:88702335 G>A maps to NM_024756.2 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:88702704 C>T maps to NM_024756.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr22:28194935 C>T maps to NM_002430.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr22:28193261 G>A maps to NM_002430.2 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:28146974 G>A maps to NM_002430.2 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:158813812 G>A maps to NM_002432.1 K157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:56735680 G>A maps to NM_018365.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr17:2298502 A>G maps to NM_020310.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2078367 G>A maps to NM_130807.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:33779930 G>A maps to NM_017947.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr6:39877612 C>A maps to ENST00000425303 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr5:52394452 G>A maps to NM_004531.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr6:29627138 G>C maps to NM_002433.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr11:75438517 C>A maps to NM_025098.2 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100839364 G>A maps to NM_178176.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74688820 G>A maps to NM_006302.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:62946845 G>A maps to ENST00000393630 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr12:62902190 A>G maps to ENST00000393630 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:108724126 G>A maps to NM_014429.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:108754262 G>A maps to NM_014429.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A722-01A-12D-A364-08 chr3:108698423 C>A maps to NM_014429.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr23:102931651 T>C did not map to a codon.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr23:102931634 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr12:122107368 T>C maps to NM_173855.4 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr10:99376043 C>T maps to NM_001098831.1 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:100212598 G>A maps to NM_023948.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:113239369 C>A maps to NM_020963.3 Y700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr22:50555696 C>T maps to NM_018995.2 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50547192 C>T maps to NM_018995.2 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50552163 G>A maps to NM_018995.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50584140 G>A maps to NM_018995.2 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr22:50582665 C>T maps to NM_018995.2 F833F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:132645228 T>G maps to NM_015529.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr11:58979776 T>G maps to NM_001039396.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr11:58979711 G>A maps to NM_001039396.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr2:71361866 T>C maps to NM_005791.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43812589 C>T maps to NM_005373.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr17:56349038 G>A maps to ENST00000340482 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:56349137 C>T maps to ENST00000340482 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr23:154020487 C>T did not map to a codon.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr17:41957293 G>A maps to NM_005374.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr17:41879197 C>T maps to ENST00000398393 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:28358763 G>A maps to NM_173496.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr2:27535938 C>T maps to ENST00000405983 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr11:118133771 C>A maps to NM_144765.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:60754669 C>T maps to NM_006039.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:60749094 C>T maps to NM_006039.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:60767658 C>T maps to NM_006039.3 C1295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:3249705 G>A maps to ENST00000328215 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:3249774 C>T maps to ENST00000328215 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr11:18956229 C>T maps to NM_147199.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr11:18955896 C>G maps to NM_147199.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr11:19077805 G>A maps to NM_054030.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr4:78815324 C>T maps to NM_020236.3 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:55059976 G>T maps to NM_014175.3 G197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr2:75879652 T>C maps to NM_014763.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr6:43023653 G>A maps to NM_015950.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:43024049 G>T maps to NM_015950.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr16:418563 C>T maps to NM_006428.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:131186991 C>T maps to ENST00000425847 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:131220552 G>A maps to ENST00000425847 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:73897875 G>A maps to NM_032478.3 R170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr3:179320487 C>A maps to NM_020409.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr19:3762706 C>G maps to NM_172251.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr6:30593483 C>T maps to NM_014046.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:84377253 C>T maps to NM_016067.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr9:138392970 T>A did not map to a codon.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr7:43906438 G>A maps to NM_032014.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr2:105706376 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:10622543 C>T maps to NM_001098579.1 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB20-01A-12D-A41K-08 chr11:60285573 C>T maps to NM_001012417.2 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr11:60164140 T>C maps to NM_032597.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:60482850 A>G maps to NM_031457.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr2:17998085 C>T maps to NM_001105569.1 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr2:47637342 A>G maps to NM_000251.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr1:76333273 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:48026078 G>A maps to NM_000179.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:48026576 G>A maps to NM_000179.2 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:120791156 G>T maps to NM_002442.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:55339543 G>A maps to NM_138962.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:135913889 G>T maps to NM_018133.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:234775650 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:234774970 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr23:64949441 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr8:10285773 C>T maps to NM_012331.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr3:49725283 C>T maps to NM_020998.3 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr3:49928942 C>T maps to NM_002447.2 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49940295 G>A maps to NM_002447.2 Y249Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:131207113 T>A did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:131188792 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:131188700 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr2:190922013 C>T maps to NM_005259.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:155582955 G>A maps to NM_018116.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:174156453 C>T maps to NM_002449.4 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:56672670 C>T maps to NM_005946.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr16:56659783 C>T maps to ENST00000330439 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr9:21854676 G>A maps to NM_002451.3 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:121528317 G>A maps to NM_022045.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr23:154294020 G>C did not map to a codon.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr8:98657099 G>A maps to NM_178812.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr8:97269340 T>C maps to NM_015942.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr2:242039185 C>A maps to NM_182501.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr8:66619311 T>C maps to NM_014637.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr8:66619383 C>A maps to NM_014637.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr8:66605934 G>A maps to NM_014637.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr6:151239755 C>T maps to NM_015440.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:86582120 T>C maps to NM_001159377.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:28014242 G>A maps to NM_152912.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr11:68480779 G>T maps to NM_004923.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:149831995 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:149787587 C>T did not map to a codon.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr23:149895774 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:149902421 T>C maps to NM_001145862.1 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:9739505 C>A maps to NM_001077525.2 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr15:31197978 T>C maps to NM_014967.4 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr11:95580966 G>A maps to NM_016156.5 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr11:95595462 A>G maps to NM_016156.5 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:30416461 C>A maps to NM_021090.3 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr22:30416350 G>A maps to NM_021090.3 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr17:56585535 G>A maps to NM_004687.4 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr17:56582843 C>T maps to NM_004687.4 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr17:56572508 C>A maps to NM_004687.4 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:56582921 G>A maps to NM_004687.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:17169088 C>T maps to NM_004686.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:63488556 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:63488626 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:11163707 C>T maps to NM_015458.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr4:187455415 C>T maps to NM_005958.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr1:11169350 G>T maps to NM_004958.3 L2508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr1:11189829 G>C maps to NM_004958.3 S1893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr1:11190606 C>T maps to NM_004958.3 P1864P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr4:100534203 C>T maps to ENST00000511045 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr4:100543848 G>A maps to ENST00000511045 K870K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr8:17611560 G>A maps to NM_001001924.2 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr13:29599578 C>T maps to NM_001033602.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr13:29598981 C>T maps to NM_001033602.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:29598969 C>T maps to NM_001033602.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr11:26586955 A>G maps to NM_001135091.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:9071590 G>T maps to NM_024690.2 P5285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr19:9075832 C>T maps to NM_024690.2 E3871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr19:9082694 T>A maps to NM_024690.2 T3040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr19:9057079 G>T maps to NM_024690.2 I10122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr19:9058118 G>C maps to NM_024690.2 S9776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr19:9087659 G>A maps to NM_024690.2 T1385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr19:9005697 G>A maps to NM_024690.2 D13236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:9086743 T>A maps to NM_024690.2 R1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr19:9063010 C>T maps to NM_024690.2 V8145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr19:9086804 A>G maps to NM_024690.2 S1670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr19:9045762 G>A maps to NM_024690.2 T11956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr19:9089954 G>A maps to NM_024690.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr19:9069613 G>A maps to NM_024690.2 S5944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:9066184 A>G maps to NM_024690.2 S7087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:9066187 G>A maps to NM_024690.2 S7086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:9075007 T>C maps to NM_024690.2 S4146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr19:9087740 G>A maps to NM_024690.2 S1358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr19:9057372 A>G maps to NM_024690.2 L10025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr19:9057379 A>T maps to NM_024690.2 S10022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr7:100682352 C>A maps to NM_001040105.1 I2552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr7:100693834 T>C maps to NM_001040105.1 L4265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr7:100684107 C>A maps to NM_001040105.1 T3137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr7:100681500 C>T maps to NM_001040105.1 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr7:100683804 A>T maps to NM_001040105.1 I3036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr7:100682271 G>A maps to NM_001040105.1 T2525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr7:100682920 C>T maps to NM_001040105.1 R2742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100678674 C>T maps to NM_001040105.1 S1326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr7:100701286 C>T maps to NM_001040105.1 R4482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr11:1081736 C>T maps to ENST00000441003 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:195452856 G>A maps to ENST00000447234 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:195475930 G>A maps to NM_018406.5 N5292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:1266203 G>A maps to ENST00000447027 T2701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr11:1255480 G>A maps to ENST00000447027 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr11:1271276 C>G maps to ENST00000447027 T4392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr11:1263452 G>A maps to ENST00000447027 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:1256377 C>T maps to ENST00000447027 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:1267115 G>A maps to ENST00000447027 T3005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:1268945 C>T maps to ENST00000447027 P3615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:1248356 C>T maps to ENST00000447027 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:1250941 G>A maps to ENST00000447027 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr11:1025071 G>T maps to NM_005961.2 C999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr11:1018411 G>T maps to NM_005961.2 I1463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr11:1029108 G>A maps to NM_005961.2 Y439Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr4:71346946 A>G maps to NM_152291.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr4:71346916 T>A maps to NM_152291.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:71339747 C>T maps to NM_152291.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:20827308 G>T maps to NM_024544.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:20828656 C>T maps to NM_024544.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65633302 C>A maps to NM_025128.4 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr6:49412359 A>C maps to NM_000255.3 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:110034288 C>T maps to NM_001114185.1 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:29853337 G>A maps to NM_017458.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr21:42748855 G>A maps to NM_002463.1 W8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr10:112039788 C>T maps to NM_130439.3 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr23:3242965 C>A did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr23:3227795 G>A did not map to a codon.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr23:3228395 G>A did not map to a codon.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr23:3229595 G>A did not map to a codon.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr23:3235404 G>C did not map to a codon.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr23:3229354 G>A did not map to a codon.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr23:3240658 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:3235283 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:3240296 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr23:3240571 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr23:3238697 C>T did not map to a codon.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:3227765 G>C did not map to a codon.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr23:3228256 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr23:3240712 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:4451273 G>A maps to NM_001105538.1 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:4451487 G>A maps to NM_001105538.1 N558N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:42320928 C>T maps to NM_002466.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr12:102072012 T>A maps to NM_002465.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:47353710 C>T maps to ENST00000399249 K1242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr1:203138380 C>T maps to NM_004997.2 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr13:77738586 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:77713378 G>A maps to NM_015057.4 C2537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:77835489 G>A maps to NM_015057.4 Y556Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr17:48600355 C>A maps to NM_032133.4 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr6:153043115 C>T maps to NM_025107.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:38182002 C>T maps to NM_001172567.1 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr12:81110949 G>T maps to NM_005593.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:10404783 C>T maps to NM_005963.3 E1127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr17:10408610 A>G maps to NM_005963.3 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:15826540 C>T maps to NM_001040114.1 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr16:15814135 G>A maps to NM_001040114.1 R1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr17:10222451 C>T maps to NM_003802.2 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr17:10258002 C>T maps to NM_003802.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr19:50752254 G>A maps to NM_001145809.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50783374 G>T maps to NM_001145809.1 E1372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50792778 G>A maps to NM_001145809.1 L1613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:108229288 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:108112994 G>A maps to NM_014981.1 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr3:108156456 C>G maps to NM_014981.1 R1075R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:108175704 T>C maps to NM_014981.1 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:10430103 G>A maps to NM_017534.5 N1333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:10448738 G>A maps to NM_017534.5 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FO-01A-21D-A364-08 chr17:10428897 C>T maps to NM_017534.5 T1469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr17:10442557 G>T maps to NM_017534.5 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr17:10435045 G>A maps to NM_017534.5 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr17:10446276 C>T maps to NM_017534.5 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr17:10447216 A>T did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:10355524 G>A maps to NM_017533.2 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr17:10355470 G>A maps to NM_017533.2 F1175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr17:10353813 G>A maps to NM_017533.2 Y1379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:23858174 C>T maps to NM_002471.3 K1356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr14:23887453 G>A maps to NM_000257.2 D1378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr14:23887534 C>T maps to NM_000257.2 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr14:23885341 G>T maps to NM_000257.2 R1608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr14:23901869 G>A maps to NM_000257.2 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:23888704 C>T maps to NM_000257.2 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:33589833 G>A maps to NM_020884.3 A1962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr17:10296219 C>T maps to NM_002472.2 Q1797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr22:36696286 C>T maps to NM_002473.4 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr22:36680209 G>A maps to NM_002473.4 R1898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:36710261 G>A maps to NM_002473.4 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:36714302 C>T maps to NM_002473.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr22:36715608 G>A maps to NM_002473.4 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr18:3255825 C>T maps to NM_006471.2 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:35176564 C>T maps to NM_006097.3 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr6:16146915 T>A maps to NM_013262.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:16143928 G>T did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr3:123456318 G>T maps to NM_053025.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr3:123383036 C>T maps to NM_053025.3 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:123426764 G>A maps to NM_053025.3 C742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:123419104 G>A maps to NM_053025.3 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:123426764 G>A maps to NM_053025.3 C742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr6:2680488 G>A maps to NM_001012418.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:16675190 G>A maps to NM_012334.2 L1579L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:16694489 G>A maps to NM_012334.2 R1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:16780630 A>G did not map to a codon.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr17:18052095 C>T maps to ENST00000205890 R2262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr13:109779875 G>A maps to NM_015011.1 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:109779683 C>T maps to NM_015011.1 C1257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:27437498 C>T maps to NM_078471.3 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:27448160 G>A maps to NM_078471.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:26164704 C>T maps to ENST00000407587 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:26173713 G>A maps to ENST00000407587 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:26291195 C>T maps to ENST00000407587 C1541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr17:34854316 C>T maps to NM_001163735.1 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr12:57435233 G>A maps to NM_005379.2 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:192225387 G>A maps to NM_001130158.1 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:30986137 G>A maps to NM_015194.1 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr15:59480399 G>A maps to NM_004998.2 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:8612973 G>A maps to NM_012335.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:8612934 G>A maps to NM_012335.3 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:8613156 G>A maps to NM_012335.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:109876339 G>A did not map to a codon.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr10:26446394 C>T maps to NM_017433.4 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr10:26462762 A>G maps to NM_017433.4 K1190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:26455001 C>T maps to NM_017433.4 Y1002Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:26463096 G>T maps to NM_017433.4 E1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr10:26377233 G>T maps to NM_017433.4 G488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:26463213 C>T maps to NM_017433.4 Q1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr2:171056736 T>A maps to NM_138995.3 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:47363954 G>A maps to NM_001080467.2 N1690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:76604977 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:76568664 C>T maps to ENST00000428345 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr11:76868350 G>A maps to NM_000260.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:76893184 C>T maps to NM_000260.3 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr2:128335736 C>T maps to ENST00000389524 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr2:128335754 C>T maps to ENST00000389524 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:128322878 C>T maps to ENST00000389524 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:128331594 C>T maps to ENST00000389524 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr19:17265123 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:17270254 C>T maps to NM_004145.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr1:171605565 G>A maps to NM_000261.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr18:3135566 C>A maps to NM_003803.3 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr18:3102499 G>A maps to NM_003803.3 R1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:3215101 G>A maps to NM_003803.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr8:2021548 C>T maps to NM_003970.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:2026841 G>A maps to NM_003970.2 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:2048705 G>A maps to NM_003970.2 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr1:24419566 C>T maps to ENST00000330966 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr10:69961682 C>T maps to NM_032578.2 G1197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:69957222 G>A maps to NM_032578.2 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr10:69881644 T>C maps to NM_032578.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr19:46393883 C>T maps to NM_001012643.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr3:40231653 G>A maps to NM_015460.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:59147848 A>T maps to NM_001085487.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:41795086 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:41801447 C>T maps to NM_006766.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr10:76788960 T>G maps to NM_012330.2 L1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:76732344 C>T maps to NM_012330.2 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr2:1926498 C>A maps to ENST00000399161 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr4:40123038 C>A maps to NM_018177.3 S1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr21:30255332 A>G maps to NM_013240.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:140264114 G>A did not map to a codon.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr12:112528659 C>T maps to NM_024953.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:112516058 A>G maps to NM_024953.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr3:175042114 G>A did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr3:175041962 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr12:57112064 T>C maps to NM_001113203.1 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr12:57112271 C>T maps to NM_001113203.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr12:57112088 G>A maps to NM_001113203.1 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:57113480 A>G maps to NM_001113203.1 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:13249042 C>T maps to NM_052876.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:13246944 C>T maps to NM_052876.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:71169581 C>T maps to NM_018161.4 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:71193051 C>T maps to NM_018161.4 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:66852501 G>A maps to ENST00000359087 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:42085836 C>T maps to NM_153006.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr13:102047575 C>T maps to NM_052867.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:101717892 G>A maps to NM_052867.2 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr4:89618404 G>A maps to NM_153757.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144659249 G>A maps to ENST00000276844 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S0-01A-11D-A41K-08 chr19:50868848 C>T maps to NM_004851.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:80417914 C>T maps to ENST00000374611 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:80417932 C>T maps to ENST00000374611 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:60740234 G>A maps to NM_024611.4 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr11:78277281 C>A maps to NM_024678.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr3:50334945 A>C maps to NM_012191.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:201618017 C>T maps to ENST00000367296 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr1:201777623 G>A maps to ENST00000367296 S1308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr11:20005784 C>T maps to ENST00000396087 D943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr12:78515854 G>T maps to NM_014903.4 T1295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr12:78362363 C>T maps to NM_014903.4 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:15468433 C>T maps to NM_015909.2 G1450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:15378657 C>T maps to NM_015909.2 E1959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr2:15432833 G>A maps to NM_015909.2 H1618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr2:15358959 G>A maps to NM_015909.2 D2123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:35770247 G>A maps to ENST00000400445 T1725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr13:35733541 G>A maps to ENST00000400445 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:204039931 C>G maps to NM_001114132.1 S2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:47036898 A>G maps to NM_015175.1 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr3:47038460 C>A maps to NM_015175.1 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr3:47037251 C>T maps to NM_015175.1 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:47041141 G>A maps to NM_015175.1 L1242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:47042567 C>T maps to NM_015175.1 S1461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:47049879 C>T maps to NM_015175.1 S2609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:90993093 G>A maps to NM_002485.4 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr8:90955506 C>A maps to NM_002485.4 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16893672 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16893829 G>A maps to NM_017940.3 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16895568 G>A maps to NM_017940.3 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16895688 G>A maps to NM_017940.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr1:16893755 T>C maps to NM_017940.3 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr1:145325996 A>G maps to NM_001039703.4 Q1290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr1:148004649 T>C maps to ENST00000310701 E893E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:148594438 A>G maps to NM_001170755.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr1:21798094 A>G maps to NM_032264.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:21795388 C>T maps to NM_032264.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr1:144821953 C>G maps to NM_001037675.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:41345492 G>A maps to NM_005899.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr21:22782675 G>A maps to NM_004540.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr21:22804446 T>A maps to NM_004540.2 Y500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr19:19356216 C>T maps to NM_004386.2 N1196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:19338462 T>C maps to NM_004386.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19329841 G>A maps to NM_004386.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19339179 G>A maps to NM_004386.2 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr11:134054636 C>T maps to NM_015261.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr7:158443615 G>A maps to NM_017760.5 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr9:100431228 A>G maps to NM_002486.4 Q706Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr19:39691042 G>A maps to NM_001001414.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr1:36028871 G>T maps to NM_001014839.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr1:36026231 G>T maps to NM_001014839.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr22:37263491 C>T maps to NM_013416.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr22:37266569 G>A maps to NM_013416.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr22:37263464 C>T maps to NM_013416.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr22:37260172 T>C did not map to a codon.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr2:106497793 G>A maps to NM_001004720.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:183846058 A>G maps to NM_205842.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:183847592 A>G maps to NM_205842.1 H394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:133540273 C>T maps to NM_207363.2 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:133538753 A>G maps to NM_207363.2 A1640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:133489409 G>T maps to NM_207363.2 R1781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:50190189 G>A maps to NM_001037806.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr2:232320220 A>G maps to NM_005381.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr8:71126309 G>A maps to NM_006540.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:71068945 A>G maps to NM_006540.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:71069249 C>T maps to NM_006540.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MK-01A-11D-A364-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr10:51584845 G>A maps to NM_001145260.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr10:51584629 C>G maps to NM_001145260.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr10:51584700 C>G maps to NM_001145260.1 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr20:33345722 C>T maps to NM_014071.2 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr17:15976857 A>C maps to ENST00000395857 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:15971375 G>A maps to ENST00000395857 Q1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr17:15989709 G>A maps to ENST00000395857 G1037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:15971250 C>T maps to ENST00000395857 T1582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:124824935 G>A maps to NM_006312.4 R1805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr12:124824555 G>A maps to NM_006312.4 L1902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:124857100 G>A maps to NM_006312.4 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr6:31557640 G>A maps to NM_147130.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:160314572 C>A maps to NM_015331.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:2573007 C>T maps to NM_006101.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr16:15771719 C>G maps to NM_001143979.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:15771785 C>T maps to NM_001143979.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr17:8350175 G>T maps to ENST00000402554 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:23931680 G>A maps to NM_002487.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr15:23932058 C>T maps to NM_002487.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:134292491 G>A maps to NM_006096.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr16:58545389 G>A maps to NM_001130487.1 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:149907853 C>T maps to NM_001543.4 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:75565361 G>A maps to NM_003635.3 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr4:118975474 T>A maps to NM_004784.2 L137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:115997286 C>T maps to NM_022569.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr3:179341803 T>A maps to NM_002492.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:161183491 C>T maps to NM_004550.4 C422C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:47606017 G>A maps to NM_004551.2 K260K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:1814478 G>A maps to ENST00000469176 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:67375931 C>T maps to NM_007103.3 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:152484039 G>A maps to NM_001164507.1 S3380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr2:152420176 C>G maps to NM_001164507.1 V6212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr2:152359339 C>T maps to NM_001164507.1 E7965E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:152364587 C>T maps to NM_001164507.1 S7794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:21120416 G>A maps to ENST00000430741 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr20:32248141 C>A maps to NM_031232.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr12:8242591 A>G maps to NM_015509.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr1:16778445 T>C maps to NM_018090.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:11185820 T>C maps to NM_006403.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr6:11213710 G>A maps to NM_006403.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr15:75644727 G>A maps to NM_024608.2 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr4:170482701 C>A maps to ENST00000507142 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:170321764 G>A maps to ENST00000507142 C1207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:170459006 G>A maps to ENST00000507142 R540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:127113177 C>T maps to NM_001166171.1 Y332Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr1:198233328 A>G maps to NM_133494.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:75558140 G>A maps to NM_033116.4 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:75563872 C>T maps to NM_033116.4 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr11:20869194 G>A maps to NM_006157.3 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:45000982 T>C maps to NM_001145107.1 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr15:73528784 A>C maps to NM_002499.3 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:73541549 G>A did not map to a codon.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr10:5497026 C>A maps to NM_001047160.1 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr18:70461399 G>A maps to NM_153181.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr18:70526273 C>A maps to NM_153181.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr2:233898823 A>C did not map to a codon.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr2:233899064 C>T maps to NM_005383.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr2:233899739 C>A maps to NM_005383.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr2:242757476 T>A maps to NM_001167599.1 C199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr10:105330663 C>A maps to NM_004210.4 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:105331340 G>A maps to NM_004210.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:7224436 G>A maps to NM_032442.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:7221198 G>A maps to NM_032442.2 C1371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr17:7222512 G>A maps to NM_032442.2 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:182542960 C>T maps to NM_002500.2 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr17:37762552 C>A maps to NM_006160.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:55420975 C>A maps to NM_021191.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr7:31378576 G>A maps to NM_022728.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr17:29576013 A>G maps to NM_001042492.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr1:204926874 C>T maps to ENST00000367172 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr1:204951035 C>T maps to ENST00000367172 Y786Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr1:204985657 T>C maps to ENST00000367172 S1345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr1:204937482 C>T maps to ENST00000367172 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr16:69727846 T>C maps to NM_138713.2 S1373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:77193713 G>A maps to NM_172387.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr18:77170781 G>A maps to NM_172387.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:68200916 C>A maps to NM_173165.2 C591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr1:61818240 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:14125765 C>A did not map to a codon.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr19:3452609 G>A maps to ENST00000269778 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr9:94172249 G>C maps to NM_005384.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39398151 C>T maps to NM_002503.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145659036 G>A maps to NM_013432.4 Q1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145667731 G>A maps to NM_013432.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:101572707 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:34262434 G>A maps to NM_021100.4 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:41062194 C>T maps to NM_002505.4 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:104517075 G>A maps to NM_006166.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:47583667 G>A maps to NM_002507.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr17:47583676 C>T maps to NM_002507.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:25761537 G>A maps to NM_018297.3 R586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:103822450 G>T maps to NM_139173.3 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:103947621 G>A maps to NM_178833.4 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:103970156 G>A maps to NM_178833.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr10:115636277 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr5:177577923 G>A maps to NM_017838.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A722-01A-12D-A364-08 chr22:42071071 G>A maps to ENST00000402458 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr23:17750101 A>G did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr23:17705983 G>A did not map to a codon.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr23:17744785 C>T did not map to a codon.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr23:17739682 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:52481973 C>T maps to NM_007361.3 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr14:52508860 A>T maps to NM_007361.3 L596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:52509598 G>A maps to NM_007361.3 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr14:51224909 C>T maps to NM_020921.3 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr9:95888797 G>A maps to NM_004148.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr12:772598 C>T maps to NM_016533.4 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:25472046 G>A maps to NM_025176.4 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:69375507 C>T maps to NM_016101.4 Q166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:156899409 C>T maps to NM_001099287.1 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:52526218 C>T maps to NM_007184.3 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52521839 C>T maps to NM_007184.3 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr8:63659612 C>T maps to NM_173688.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr23:119077406 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:119064004 G>A did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:28227391 C>T maps to NM_001007531.1 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr6:28227526 G>A maps to NM_001007531.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:28227631 G>A maps to NM_001007531.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr5:1038079 C>T maps to NM_033120.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:51875454 G>A maps to NM_005601.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:45656260 C>A maps to NM_198478.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:36988567 G>A maps to NM_001079668.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr10:134598509 G>A maps to NM_177400.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:33462275 C>T maps to NM_018096.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7317762 C>A maps to NM_020795.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr23:70375182 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:70367894 C>T did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr23:5821236 G>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:5821329 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:5811650 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:5821328 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr17:26488194 C>T maps to NM_016231.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr5:65077142 T>C maps to NM_020726.4 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr16:3613170 G>A maps to ENST00000448023 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr16:57088674 G>A maps to NM_032206.3 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr11:7982636 C>T maps to NM_176821.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr19:56422071 G>A maps to NM_176810.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:7059987 C>T maps to NM_176822.3 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:7060963 A>G maps to NM_176822.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:7064750 G>A maps to NM_176822.3 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr1:247588839 C>T maps to NM_004895.4 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr19:56379185 C>T maps to NM_134444.4 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr19:56369967 T>A maps to NM_134444.4 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr19:56369988 C>T maps to NM_134444.4 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:56539872 A>G maps to NM_153447.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr19:56515210 G>C maps to NM_153447.4 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:55447771 C>T maps to ENST00000446217 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr19:56482026 G>A maps to NM_176811.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr19:56466878 C>T maps to NM_176811.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr19:56223889 C>A maps to NM_176820.2 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:56223302 G>A maps to NM_176820.2 C902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr11:119045199 C>T maps to NM_024618.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr11:119043648 T>C maps to NM_024618.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:142399949 G>A maps to NM_002511.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:49237345 C>T maps to ENST00000393198 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr5:137451448 C>T maps to NM_003551.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:152132078 G>A maps to NM_004688.2 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:4516289 G>A maps to NM_020677.3 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:43180470 C>T maps to NM_021079.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr4:56471441 G>A maps to NM_006681.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:114168748 C>A maps to NM_006169.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr5:43700277 T>G maps to NM_182977.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:30491787 G>A maps to NM_006092.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:30469003 G>A maps to NM_006092.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr16:50733807 C>T maps to NM_022162.1 F161F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38084896 G>A maps to NM_024313.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr18:31802971 G>T maps to NM_003787.4 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr1:6592682 T>A maps to NM_024654.4 K459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:70516422 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:70519911 C>T did not map to a codon.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:203149109 G>T maps to NM_015934.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr12:117660555 C>T maps to ENST00000338101 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr12:117685281 G>A maps to ENST00000338101 C932C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr12:117657906 G>A maps to ENST00000338101 D1415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:162313728 A>G maps to NM_014697.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr7:150699373 T>C maps to NM_000603.4 D578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:150704234 C>T maps to NM_000603.4 C661C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:139401817 G>A maps to NM_017617.3 N1194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr9:139391806 C>T maps to NM_017617.3 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139391155 G>A maps to NM_017617.3 G2345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr19:15300084 G>A maps to NM_000435.2 I397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr19:15276798 G>A maps to NM_000435.2 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:15271811 C>T maps to NM_000435.2 P2209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr6:32163813 C>T maps to NM_004557.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr6:32185011 G>A maps to NM_004557.3 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr6:32188017 G>A maps to NM_004557.3 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr6:32180341 C>A maps to NM_004557.3 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr17:79910953 C>T maps to NM_178493.5 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:26917260 T>C maps to ENST00000449198 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr19:46443951 G>A maps to NM_002516.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr23:100104283 T>C did not map to a codon.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr11:89165956 T>G maps to NM_016931.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:2030957 G>A maps to NM_172168.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:101607289 C>T maps to NM_002518.3 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:101591980 G>A maps to NM_002518.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:34268982 C>T maps to NM_001164749.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:34269141 C>T maps to NM_001164749.1 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:66192367 C>T maps to NM_178864.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66191875 C>A maps to NM_178864.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:108032026 A>G maps to NM_002519.2 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:108068118 A>G maps to NM_002519.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr20:62737950 C>T maps to NM_005286.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:62737665 G>A maps to NM_005286.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr18:21112186 G>A maps to NM_000271.4 R1272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr18:21134924 G>T maps to NM_000271.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr7:44575522 C>A maps to NM_013389.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr7:44553093 A>C maps to NM_013389.2 G1344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44579809 C>T maps to NM_013389.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr20:57290252 C>T maps to NM_024663.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr17:45668126 G>A maps to NM_006310.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:53900560 C>T maps to NM_003717.2 *114*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr2:110922635 T>A maps to NM_000272.3 K241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:5964827 C>T maps to NM_015102.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr1:5964710 G>A maps to NM_015102.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:5924496 G>A maps to NM_015102.2 G1299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:5927956 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:5965425 C>T maps to NM_015102.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr1:179526350 G>A maps to NM_014625.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:106858223 C>T maps to ENST00000503451 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr1:153661479 C>T maps to NM_000906.3 Y823Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35807106 C>T maps to NM_003995.3 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr7:98254300 C>T maps to NM_002523.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr7:98256571 C>T maps to NM_002523.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr7:98257787 C>T maps to NM_002523.2 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr7:25264784 G>A maps to NM_022150.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:164247094 C>T maps to NM_000909.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr4:164272283 A>C maps to NM_006174.2 R287R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-J9-A52C-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZG-A9N3-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr1:161203128 C>A did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr19:17343310 C>T maps to NM_005234.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:17343235 C>T maps to NM_005234.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:149356755 C>T maps to ENST00000511528 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:157186311 C>T maps to NM_006186.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr10:115364398 C>T maps to ENST00000369358 W1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr7:107880412 T>C maps to ENST00000379032 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:107834556 C>T maps to ENST00000379032 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr8:32453406 C>T maps to NM_013956.3 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr8:32599589 G>T maps to ENST00000338921 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr21:16338591 G>T maps to NM_003489.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:16339100 C>T maps to NM_003489.3 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:16339793 T>C maps to NM_003489.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:2936420 C>T maps to NM_031474.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr23:105153578 G>A did not map to a codon.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr16:67919730 C>T maps to NM_198443.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr10:33474631 G>A maps to NM_003873.5 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr2:206641225 G>A maps to NM_018534.3 E899E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FP-01A-21D-A364-08 chr2:50765423 C>A maps to ENST00000404971 G744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr2:50850691 T>C maps to ENST00000404971 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:51255225 G>A maps to ENST00000404971 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr11:64416296 G>T maps to NM_015080.3 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:80164183 C>T maps to NM_004796.4 T903T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr5:176720971 T>A maps to NM_022455.4 S2201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:176638165 G>A maps to NM_022455.4 T922T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176719085 C>T maps to NM_022455.4 L2130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr23:152037458 A>G did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr20:1433674 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:1445044 G>A maps to ENST00000476071 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:1426345 G>A maps to ENST00000476071 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr8:126163473 G>A maps to NM_173685.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:6605394 C>T maps to NM_017755.5 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr7:72717395 C>G maps to NM_001168347.1 *471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:72718230 G>A maps to NM_148956.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:18765458 G>A maps to ENST00000455492 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr10:104866419 A>C maps to NM_001134373.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr17:17250218 G>A maps to ENST00000379552 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr11:132081913 A>C did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:107961229 G>A maps to NM_001113228.1 P372P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-7230-01A-11D-2114-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:108023233 G>A maps to NM_001113226.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:108023404 C>T maps to NM_001113226.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr9:135073942 G>T maps to NM_032536.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:135073795 C>T maps to NM_032536.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:135073363 C>T maps to NM_032536.2 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:156845393 C>T maps to NM_002529.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:61340972 C>T maps to NM_002531.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:11798757 G>A maps to NM_012344.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr7:151046259 A>T maps to ENST00000355851 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:10841066 C>T maps to NM_002484.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:32142776 G>A maps to NM_025152.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49409101 G>A maps to NM_006184.5 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49416275 G>A maps to NM_006184.5 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr5:162886969 G>A maps to NM_145266.4 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr19:33183246 C>T maps to NM_001105570.1 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr9:34343326 C>T maps to NM_147173.1 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:163317626 C>T maps to NM_145697.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr11:71718447 G>A maps to ENST00000393695 S1756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr14:73750945 C>T maps to NM_001005743.1 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:69094532 C>A maps to NM_020401.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr12:69103088 G>A maps to NM_020401.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr1:229577701 G>A maps to NM_018230.2 F1140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr11:47857210 G>A maps to NM_015231.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr11:47814390 G>A maps to NM_015231.1 R1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr9:131743607 G>T maps to NM_015354.1 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr7:135279305 T>C maps to NM_015135.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:135282804 C>T maps to NM_015135.2 C708C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:13393390 C>T maps to NM_024923.2 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr3:13407499 G>A maps to NM_024923.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:13361407 T>C maps to NM_024923.2 T1746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:13381470 G>A maps to NM_024923.2 S1118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:13418954 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:154067629 A>T maps to NM_207308.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr1:154113941 G>A maps to NM_207308.2 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:154042823 G>A maps to NM_207308.2 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr9:134077100 C>T maps to ENST00000451030 G1864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:102492966 G>A maps to NM_024057.2 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50412680 G>A maps to NM_012346.4 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:73208111 C>T maps to NM_024844.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:3704645 G>A maps to NM_016320.4 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:25887830 G>A maps to NM_014089.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:23235497 C>T maps to ENST00000413919 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr16:28549402 G>A maps to NM_001042483.1 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:224482012 G>A maps to NM_002533.2 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr19:16860226 C>T maps to ENST00000438489 H258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:16908687 G>A maps to ENST00000438489 A1150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:16918718 C>T maps to ENST00000438489 S1353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr23:102337711 G>A did not map to a codon.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr23:102337985 G>A did not map to a codon.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr17:704349 G>A maps to NM_022463.3 R383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr14:24877238 C>T maps to NM_025081.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr14:24880386 G>A maps to NM_025081.2 Q840Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr12:113384759 C>T maps to NM_006187.2 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:113379553 G>A maps to NM_006187.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:113388745 G>A maps to NM_006187.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr12:113376376 C>T maps to NM_006187.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:136083532 G>A maps to NM_014581.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:136081319 G>A maps to NM_014581.2 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:228456387 C>T maps to NM_001098623.1 R1673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:228433201 G>C maps to NM_001098623.1 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr1:228481210 C>T maps to NM_001098623.1 D3675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr1:228466408 G>A maps to NM_001098623.1 V2293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:228452054 C>T maps to NM_001098623.1 A1608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:228401956 G>T maps to NM_001098623.1 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr8:133053841 G>A maps to ENST00000262283 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr8:133053366 G>A maps to ENST00000262283 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr15:28116314 C>T maps to NM_000275.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:28259960 C>T maps to NM_000275.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:28260032 G>T maps to NM_000275.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr4:48851970 T>C maps to NM_001168254.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:128723861 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr23:128724235 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr23:128679012 A>C did not map to a codon.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr8:103564149 C>T maps to NM_024410.3 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr9:131231506 C>T maps to NM_153435.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr23:123839058 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:123514534 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:123514606 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr23:123514727 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:167420176 G>A maps to NM_001122679.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr5:167673769 C>A maps to NM_001122679.1 V1933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:167642134 C>G maps to NM_001122679.1 R1303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:167489161 A>G maps to NM_001122679.1 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr5:167553795 C>A maps to NM_001122679.1 C749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:167645467 C>T maps to NM_001122679.1 N1515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr4:183714865 C>A maps to NM_001080477.1 T2347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr4:183710343 C>T maps to NM_001080477.1 Y1801Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr4:183675932 C>T maps to NM_001080477.1 L1471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:183714556 G>A maps to NM_001080477.1 Q2244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr11:78443390 T>C maps to NM_001098816.2 A1036A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr11:78381218 G>A maps to NM_001098816.2 Y2057Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr11:78380594 G>C maps to NM_001098816.2 G2265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:13778281 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44685059 C>T maps to ENST00000444676 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44733587 C>T maps to ENST00000444676 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr10:50953437 G>A maps to NM_018245.2 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr10:50953975 C>T maps to NM_018245.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:50955173 C>T maps to NM_018245.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:9796442 C>T maps to NM_016821.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr23:70767812 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:74692155 C>T maps to NM_152635.1 D504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr10:15103732 A>G maps to NM_018324.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:137990193 C>T maps to NM_014279.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:138011582 C>T maps to NM_014279.4 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr1:102269967 G>A maps to ENST00000338858 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr11:7531064 G>A maps to NM_198474.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:127549252 G>T did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr1:161967654 C>T maps to ENST00000451379 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr1:161987209 G>A maps to ENST00000451379 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:53081568 G>A maps to NM_004498.1 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr15:53080998 G>A maps to NM_004498.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr3:193332787 C>T maps to NM_130837.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:193377283 T>C maps to NM_130837.2 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:46056804 G>A maps to NM_025136.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:132306037 G>A maps to NM_002545.3 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr11:132307146 G>A maps to NM_002545.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr8:145109714 C>T maps to ENST00000360660 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145107480 G>A maps to ENST00000360660 R1058R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr23:153420112 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:241767566 G>A maps to NM_014322.2 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr20:62730103 C>T maps to NM_000913.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:154412195 C>T maps to NM_001145279.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr11:7960190 G>A maps to NM_001003745.1 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:22038125 G>A maps to NM_001005465.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr14:22038731 A>T maps to NM_001005465.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BR-01A-32D-A257-08 chr11:123886817 C>T maps to NM_001004462.1 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr11:123886346 C>T maps to ENST00000375021 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr11:123886914 C>T maps to NM_001004462.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123909642 G>A maps to NM_001004463.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr11:123909324 C>T maps to NM_001004463.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr11:123900427 C>T maps to NM_001004464.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123893784 C>T maps to NM_001001953.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr19:15852462 C>T maps to NM_013938.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr19:15852909 G>A maps to NM_013938.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:16060515 C>T maps to NM_001004465.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr1:159505650 G>A maps to NM_001004469.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:158435851 C>A maps to NM_001004473.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:158390383 G>T maps to NM_001004476.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:56030938 G>A maps to NM_206899.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr1:158450673 G>T maps to NM_001004472.1 *336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:158368836 C>T maps to NM_001004475.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr1:158369195 G>A maps to NM_001004475.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr1:158549148 T>G maps to NM_001004477.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:158576524 C>T maps to NM_001004478.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:158576872 C>T maps to NM_001004478.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr6:29395334 C>T maps to NM_013937.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr14:20666366 C>A maps to NM_001005503.1 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr14:20711207 C>T maps to NM_001004479.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr9:107361056 A>T maps to NM_001004482.1 L213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr9:107379675 T>C maps to NM_001001956.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr23:130678203 C>T did not map to a codon.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr1:247921333 C>T maps to NM_012353.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr1:247921333 C>T maps to NM_012353.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr17:3030695 A>T maps to ENST00000381953 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr9:125288735 C>A maps to ENST00000359439 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr7:143792958 C>T maps to NM_001004135.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr7:143826861 C>T maps to NM_001001659.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr7:143806867 C>T maps to NM_001005480.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:143771566 G>A maps to NM_001004488.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:99474213 G>T maps to NM_001005276.1 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr7:99474461 C>T maps to NM_001005276.1 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr11:6789257 G>A maps to NM_001004490.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:247614411 G>T maps to NM_001004492.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr1:247614681 G>A maps to NM_001004492.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:27879580 C>A maps to NM_033057.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:27925440 C>T maps to NM_012367.1 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:247695756 G>A maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr1:247695156 G>A maps to NM_198074.4 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:247694913 G>A maps to NM_198074.4 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:6913395 G>A maps to NM_003700.1 C112C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr6:29142062 T>A maps to NM_030905.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:248263255 C>T maps to NM_175911.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr1:248201937 G>T maps to NM_001004686.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr1:248224168 T>G maps to NM_001004687.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:248343967 C>T maps to NM_001004688.1 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr1:248343433 C>T maps to NM_001004688.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:248309106 C>T maps to NM_001004690.1 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr1:248487558 A>G maps to NM_001004691.1 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr1:248569714 G>A maps to NM_030904.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:248458841 T>C maps to NM_001004692.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:248458391 G>A maps to NM_001004692.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:248616337 C>T maps to NM_001004136.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:248525214 C>T maps to NM_001004696.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:248551358 C>T maps to NM_001005471.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:180582178 G>A maps to NM_206880.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr1:247654713 C>T maps to NM_001004698.2 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr17:3195618 A>G maps to ENST00000397187 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr17:3181632 G>A maps to NM_002551.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr17:3324769 T>C maps to NM_012373.2 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:3324784 C>T maps to NM_012373.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:55111452 C>A maps to NM_001005274.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DK-01A-11D-A377-08 chr11:55111530 C>T maps to NM_001005274.1 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr11:48510646 C>T maps to NM_001005512.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr11:55371195 G>A maps to NM_001004700.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr11:55371015 G>T maps to NM_001004700.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:49974309 A>C maps to NM_001001955.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr11:55340436 T>A maps to NM_001004701.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr11:48346689 C>A maps to NM_001004702.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr11:55433370 G>T maps to NM_001004704.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:56232828 C>T maps to NM_012374.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:59282921 C>T maps to NM_001004711.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:22133361 G>A maps to NM_001001912.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:20444036 C>A maps to NM_001005486.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr14:20344653 C>T maps to NM_001005501.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr14:20389697 T>A maps to NM_001005483.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:20528811 C>T maps to NM_001004717.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:20248780 G>A maps to NM_001005500.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr11:4928815 C>T maps to NM_001004749.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5345137 A>G maps to NM_033180.4 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr11:5322888 G>A maps to NM_033179.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr11:4791051 A>T maps to ENST00000380383 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:5462693 T>A maps to NM_001005288.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5410879 G>A maps to NM_001004756.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr11:5510454 T>C maps to NM_001005163.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:5080815 G>A maps to NM_001005164.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:5905956 C>T maps to NM_001005165.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5862947 G>T maps to ENST00000379946 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr11:4566998 C>T maps to NM_001004137.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5842293 C>T maps to NM_001005174.1 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr11:6048226 T>C maps to NM_001001917.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr11:59211156 C>T maps to NM_001004728.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr11:59211156 C>T maps to NM_001004728.1 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr11:59210667 C>T maps to NM_001004728.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr11:59189574 G>A maps to NM_001001954.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr11:56431733 C>T maps to NM_001004730.1 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr14:21623155 C>T maps to NM_001004731.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr14:21624013 C>G maps to NM_001004731.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:58190359 G>T maps to NM_001005566.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr9:125551978 C>T maps to NM_001001923.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr11:55541086 T>C maps to NM_001001967.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr11:55606970 T>A maps to NM_001005496.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr11:55606580 G>A maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr11:55607136 C>T maps to NM_001005496.1 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:55587827 C>A maps to ENST00000395203 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:55588007 A>G maps to ENST00000395203 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:55944980 C>T maps to NM_001005492.1 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr3:98109898 G>A maps to NM_001005516.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr11:55579004 T>A maps to NM_001004738.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:55594808 T>C maps to NM_001004739.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:56310190 C>T maps to NM_001005245.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:56258762 C>T maps to NM_001005282.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr11:7817802 C>T maps to NM_153444.1 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:56043917 C>T maps to NM_001004745.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr11:55999740 C>T maps to NM_001004746.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr11:56000286 C>T maps to NM_001004746.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr2:240969798 G>A maps to NM_001005853.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr12:55725831 C>T maps to NM_054104.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:55945168 C>G maps to NM_001005494.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr12:55794776 T>C maps to NM_001005518.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:55795142 C>A maps to NM_001005518.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:55820711 C>T maps to NM_001005183.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr1:158669836 G>T maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:158669920 T>C maps to NM_001005279.1 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr1:158687668 G>A maps to ENST00000368146 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:158725069 C>T maps to NM_001005184.1 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr1:158735833 C>A maps to NM_001005185.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr14:21109304 G>A maps to NM_001001968.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr14:21109703 C>G maps to NM_001001968.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr11:123813654 C>A maps to NM_001005187.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr1:158517226 G>A maps to NM_001005189.1 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14938094 C>A maps to NM_017506.1 *320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14910837 G>C maps to NM_198944.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr19:14910063 C>A maps to NM_198944.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:9226079 G>A maps to ENST00000293614 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr11:124252654 G>A maps to NM_001005468.1 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:124253092 G>A maps to NM_001005468.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:124267100 G>A maps to NM_001005467.1 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr11:124179753 C>T maps to NM_001002917.1 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr11:55861502 C>T maps to NM_001003750.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr11:55861283 G>A maps to NM_001003750.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:56128084 C>T maps to NM_001005205.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr11:55927528 G>A maps to NM_001004058.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr12:48920025 C>T maps to NM_001005203.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr12:48919554 C>T maps to NM_001005203.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr7:141619259 G>A maps to NM_001001656.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:56467958 C>T maps to NM_001013358.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr11:56511167 C>T maps to NM_001005284.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:102087009 G>A maps to NM_032831.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:102087258 C>T maps to NM_032831.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:88374516 C>T maps to NM_181837.2 C631C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr7:103844610 T>C maps to NM_002553.3 Q48Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:31266434 C>T maps to NM_030758.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr3:31710252 C>T maps to NM_017784.4 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:31921245 C>A maps to NM_017784.4 G120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:125271043 G>A maps to NM_022776.4 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr20:60854350 C>T maps to NM_144498.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:3128660 G>A maps to NM_020896.3 N297N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr2:179188941 C>T maps to ENST00000392505 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:83999179 C>T maps to NM_013370.3 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr8:90933336 C>T maps to NM_001126111.1 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr2:19553371 C>T maps to NM_145260.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:195955718 C>T maps to NM_152672.5 Y187Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr3:195953980 G>A maps to NM_152672.5 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:26696053 G>A maps to NM_194248.2 R1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr2:26705328 C>A maps to NM_194248.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:72926527 T>C maps to NM_178160.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr17:72926515 G>A maps to NM_178160.2 W262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:16729587 G>A maps to NM_020157.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr11:63764356 G>T maps to ENST00000422031 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:146058590 C>T maps to ENST00000447906 Q1112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr4:146058890 A>C maps to ENST00000447906 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:48792091 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:149916658 G>A maps to NM_020205.2 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr2:63282952 G>A maps to NM_014562.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:29630488 G>A maps to NM_183378.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65562112 C>T maps to NM_004561.2 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:18005393 C>T maps to NM_021220.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr5:41807483 C>T maps to NM_000436.3 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:107715135 C>T maps to NM_001198533.1 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:25833003 T>C maps to NM_017897.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:133197606 T>C maps to NM_170683.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:57137382 G>A maps to NM_002559.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr23:78216115 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr3:150932017 G>A maps to NM_014879.3 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:72945704 C>T maps to NM_176071.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:72945788 C>T maps to NM_176071.1 F195F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:72945873 C>T maps to NM_176071.1 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:72946148 C>A maps to NM_176071.1 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:72946265 C>T maps to NM_176071.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr23:69479041 G>A did not map to a codon.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr23:69478625 A>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:69478928 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:73008420 G>A maps to NM_004154.3 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr23:1584459 G>A did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:131531125 C>A maps to NM_001142599.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr5:131544973 A>G maps to NM_001142599.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:131530663 G>A maps to NM_001142599.1 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr3:49042344 G>A maps to NM_177938.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:49028270 G>A maps to NM_177938.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49027943 C>T maps to NM_177938.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49038922 G>A maps to NM_177938.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr12:56503665 G>A maps to NM_006191.2 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:25672096 A>G maps to NM_030979.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr23:90691468 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:90690629 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:105849202 G>A maps to ENST00000458164 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr6:34498307 G>A maps to NM_020804.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr22:43267419 G>A maps to NM_001184970.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:17548934 C>A maps to NM_013358.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:17418972 G>A maps to NM_007365.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:17410235 G>A maps to NM_007365.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr1:17690078 C>T maps to NM_012387.2 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:17701956 C>T maps to NM_207421.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:138457637 C>T maps to NM_002571.2 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:39879988 G>A maps to NM_019088.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39876747 G>A maps to NM_019088.2 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39879255 C>T maps to NM_019088.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:117030702 G>T maps to NM_002572.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:55117848 G>A did not map to a codon.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr23:55103898 T>A did not map to a codon.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr12:103246690 C>A maps to NM_000277.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:110439715 C>T did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr20:9546932 T>C maps to NM_177990.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr19:726158 G>A maps to NM_002579.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr11:35456158 C>G maps to NM_015430.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:56713244 C>T maps to NM_001127460.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr12:56720444 T>C maps to NM_001127460.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:56722257 G>A maps to NM_001127460.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:56716847 G>A maps to NM_001127460.2 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr13:28794429 C>T maps to NM_175854.7 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr10:91371707 C>G maps to NM_148977.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:2452329 G>A maps to ENST00000425477 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr22:50615614 G>T maps to NM_052839.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:124489287 G>A maps to NM_052959.2 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:124489569 G>A maps to NM_052959.2 E306E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr11:124489635 G>C maps to NM_052959.2 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr5:6748611 C>T maps to NM_006999.4 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr14:73719405 C>T maps to ENST00000427855 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr9:119065087 T>C maps to NM_002581.3 F1002F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr9:118950480 C>T maps to NM_002581.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr9:119106932 C>T maps to NM_002581.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:118950453 C>A maps to NM_002581.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:176526075 G>A maps to NM_020318.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:3021852 C>T maps to NM_152341.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr16:3021257 C>T maps to NM_152341.3 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr1:156213663 C>T maps to NM_024897.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:52268631 C>T maps to ENST00000361841 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:52268841 C>A maps to ENST00000361841 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr3:142681386 G>A maps to NM_198504.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr10:34606222 A>T maps to NM_019619.3 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr16:67694961 T>C maps to NM_016948.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:49354419 G>A maps to NM_032521.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr6:162622177 C>T maps to NM_004562.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr3:183547481 G>A maps to NM_018622.5 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:75938007 G>A maps to NM_015393.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:14693775 G>A maps to NM_002582.2 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:226551699 C>T maps to NM_001618.3 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145058756 G>A maps to NM_032789.3 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:139724617 C>T maps to NM_022750.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:122433211 C>A maps to NM_017554.2 S1312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr13:25021263 G>A maps to NM_006437.3 Q1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr13:25044067 G>A maps to NM_006437.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:25026728 A>T maps to NM_006437.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:72533876 G>A maps to NM_020214.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr3:122259685 G>C maps to NM_031458.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr22:44532374 G>A maps to NM_001003828.1 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr23:150832694 C>G did not map to a codon.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr23:150828275 C>G did not map to a codon.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr23:150840967 A>G did not map to a codon.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr23:150770052 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr23:150791529 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:150842562 C>T did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:242066483 C>A maps to ENST00000358649 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr11:125647895 C>T maps to NM_212555.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:21687106 C>T maps to NM_006192.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr11:31815068 G>A maps to NM_001604.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr11:31815293 C>T maps to NM_001604.4 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr1:18961618 G>T maps to NM_002584.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:113977702 G>A maps to NM_003466.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:37145537 C>T maps to NM_006194.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:154767948 G>A maps to NM_007349.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:27678145 G>A maps to NM_018492.2 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:138539133 C>T maps to NM_021635.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr3:52682416 T>G maps to ENST00000296302 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr3:52598070 G>A maps to ENST00000296302 Y1290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:164761812 C>T maps to NM_002585.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:154918556 C>T maps to NM_020524.2 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr11:66620018 G>A maps to NM_022172.2 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr21:47349907 C>T maps to NM_020528.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr3:51992214 G>A maps to NM_033010.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr3:51992298 G>A maps to NM_033010.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:101077939 G>A maps to NM_000282.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr5:141242916 C>T maps to NM_032420.2 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr23:91132875 G>T did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr23:91132586 G>A did not map to a codon.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr23:91133812 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr23:91133931 G>A did not map to a codon.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr23:91090585 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:91873426 T>A did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr24:4925415 G>A did not map to a codon.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr24:4967493 T>A did not map to a codon.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr24:4966871 C>T did not map to a codon.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr24:4968732 C>T did not map to a codon.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr24:4968184 G>T did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr24:4925455 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr24:4967194 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr24:4925223 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr24:4967264 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr5:141334956 C>T maps to NM_016580.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr10:56287577 G>T maps to NM_001142763.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr10:55587259 G>C maps to NM_001142763.1 P1425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:55569171 G>A maps to NM_001142769.1 F1551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr10:55955441 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:138451633 C>A maps to NM_019035.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr4:138452261 T>C maps to NM_019035.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:138442182 C>T maps to NM_019035.3 *1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:99662412 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr23:99551704 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr23:99662942 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:99662412 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:30725230 G>A maps to NM_001173523.1 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr13:53419057 C>T maps to NM_002590.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr13:67205384 C>T maps to NM_203487.2 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:67802359 C>T maps to NM_203487.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr5:140168037 G>T maps to NM_018900.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr5:140165934 C>A maps to NM_018900.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140237081 G>A maps to NM_018901.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr5:140235917 C>T maps to NM_018901.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:140250898 G>A maps to NM_018902.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr5:140250250 G>A maps to NM_018902.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140249998 G>A maps to NM_018902.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140250646 C>T maps to NM_018902.3 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:140256667 G>A maps to NM_018903.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr5:140255779 G>A maps to NM_018903.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140256124 G>A maps to NM_018903.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr5:140263148 G>A maps to NM_018904.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140263535 C>T maps to NM_018904.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:140176552 G>A maps to NM_018905.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr5:140176000 G>A maps to NM_018905.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr5:140175877 C>T maps to NM_018905.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140182314 C>T maps to NM_018906.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr5:140182440 G>A maps to NM_018906.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:140188640 C>T maps to NM_018907.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140188928 C>T maps to NM_018907.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr5:140187068 C>T maps to NM_018907.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr5:140188232 C>T maps to NM_018907.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr5:140188442 C>T maps to NM_018907.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr5:140188583 C>T maps to NM_018907.2 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140188301 G>A maps to NM_018907.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr5:140202763 G>A maps to NM_018908.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140203081 C>T maps to NM_018908.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr5:140202970 C>T maps to NM_018908.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:140201644 C>T maps to NM_018908.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr5:140203513 C>T maps to NM_018908.2 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr5:140209757 G>T maps to NM_018909.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr5:140209517 G>A maps to NM_018909.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr5:140209184 G>A maps to NM_018909.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr5:140209376 G>A maps to NM_018909.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr5:140209184 G>T maps to NM_018909.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140209589 C>T maps to NM_018909.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr5:140215503 G>T maps to NM_018910.2 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr5:140215500 C>T maps to NM_018910.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr5:140215956 C>T maps to NM_018910.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140222183 C>T maps to NM_018911.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B2-01A-12D-A32B-08 chr5:140222516 G>A maps to NM_018911.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr5:140222413 C>A maps to NM_018911.2 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:140229646 T>C maps to NM_031857.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140229396 C>A maps to NM_031857.1 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr5:140229522 C>T maps to NM_031857.1 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr5:140308817 C>T maps to NM_018898.3 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr5:140347664 G>A maps to NM_018899.5 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:140431843 G>A maps to NM_013340.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr5:140432440 A>C maps to NM_013340.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr5:140431177 C>T maps to NM_013340.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140431762 C>T maps to NM_013340.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr5:140432291 G>T maps to NM_013340.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr5:140573540 C>T maps to NM_018930.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:140572700 A>G maps to NM_018930.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr5:140574344 C>T maps to NM_018930.3 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:140595971 A>G maps to NM_018933.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140594168 C>T maps to NM_018933.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr5:140626633 G>A maps to NM_018935.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr5:140627359 C>T maps to NM_018935.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140627137 C>T maps to NM_018935.2 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140627233 G>A maps to NM_018935.2 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr5:140563339 C>A maps to NM_020957.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr5:140563060 C>T maps to NM_020957.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr5:140475282 G>T maps to NM_018936.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr5:140474538 G>T maps to NM_018936.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr5:140476344 C>T maps to NM_018936.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140475093 C>T maps to NM_018936.2 N240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr5:140502261 C>T maps to NM_018938.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140516575 C>T maps to NM_015669.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr5:140517014 C>T maps to NM_015669.2 Q667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr5:140516146 C>T maps to NM_015669.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140516632 G>A maps to NM_015669.2 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr5:140531961 G>A maps to NM_018939.2 A708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr5:140531640 G>A maps to NM_018939.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr5:140531919 G>A maps to NM_018939.2 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr5:140530896 C>T maps to NM_018939.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140554609 C>T maps to NM_018940.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr5:140553172 G>T maps to NM_018940.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FE-01A-12D-A33T-08 chr5:140554116 C>T maps to NM_018940.2 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140552433 G>A maps to NM_018940.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:140558061 T>A maps to NM_019120.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140712515 C>T maps to NM_018912.2 H755H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr5:140712440 C>T maps to NM_018912.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr5:140712482 C>T maps to NM_018912.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140712161 G>A maps to NM_018912.2 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140794394 G>A maps to NM_018913.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr5:140795087 G>A maps to NM_018913.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140795117 C>T maps to NM_018913.2 N792N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr5:140811042 A>G maps to NM_003735.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr5:140810550 C>T maps to NM_003735.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140725402 C>T maps to NM_018916.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140735372 C>T maps to NM_018917.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr5:140735009 C>T maps to NM_018917.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140744943 C>T maps to NM_018918.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140755557 C>T maps to NM_018919.2 D636D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:140773099 G>A maps to NM_032088.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr5:140773888 G>A maps to NM_032088.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr5:140772817 G>A maps to NM_032088.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr5:140783253 G>T maps to NM_018921.2 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:140729949 C>T maps to NM_018922.2 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140731332 C>T maps to NM_018922.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140731725 G>A maps to NM_018922.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140741804 G>A maps to NM_018923.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr5:140741285 C>T maps to NM_018923.2 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140751253 G>A maps to NM_018924.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140750488 G>A maps to NM_018924.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140750263 G>A maps to NM_018924.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140768944 G>A maps to NM_003736.2 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr5:140769421 G>A maps to NM_003736.2 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr5:140789301 C>T maps to NM_018926.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr5:140798187 C>T maps to NM_018927.2 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140799297 C>T maps to NM_018927.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140856592 C>T maps to NM_002588.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140857026 C>T maps to NM_002588.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr5:140865885 C>T maps to NM_018928.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:113849440 T>C did not map to a codon.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr20:44575999 C>T maps to NM_022104.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr7:82544134 C>T maps to NM_033026.5 R4389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:82545751 C>T maps to NM_033026.5 Q3850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:82581481 G>A maps to NM_033026.5 P2929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr7:82545906 G>A maps to NM_033026.5 R3799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr7:82430882 T>C maps to NM_033026.5 Q4986Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr7:82545840 G>A maps to NM_033026.5 R3821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr7:82764228 A>G maps to NM_033026.5 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr20:5099413 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr21:47851558 A>G maps to NM_006031.5 S2727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr21:47831938 C>A maps to NM_006031.5 A1984A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:47851714 C>T maps to NM_006031.5 C2779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr21:47773069 G>A maps to NM_006031.5 Q503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:71514562 G>A maps to NM_014982.2 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr14:71485737 C>T maps to NM_014982.2 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:233190172 G>A maps to NM_014801.3 Q1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:233190116 G>A maps to NM_014801.3 G1416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:233353642 A>G did not map to a codon.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr1:233394211 G>A maps to NM_014801.3 Q466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65396389 G>A maps to NM_032223.2 R1304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr21:41301035 G>C maps to NM_006198.2 *63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr5:95728926 C>T maps to NM_000439.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr20:17446196 G>T maps to NM_002594.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:17410082 C>T maps to NM_002594.2 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr15:101938638 A>C maps to NM_002570.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:101906537 C>A did not map to a codon.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr11:117090339 G>A maps to NM_004716.2 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:55521762 C>T maps to NM_174936.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr5:148747556 G>A maps to NM_024028.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:195975093 C>T maps to NM_005017.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr23:24690705 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:242794938 G>T maps to NM_005018.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:105203742 C>T maps to NM_014976.1 G1732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:771081 G>A maps to NM_182612.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:165756960 G>T maps to NM_001130690.1 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:165801935 C>A maps to NM_001130690.1 G555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr7:31862843 C>T maps to NM_001191057.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr11:72293526 G>A maps to NM_002599.3 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:10570422 G>A maps to NM_001111307.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr1:66384362 G>C maps to NM_001037341.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr1:144916718 G>A maps to NM_014644.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr1:144881610 C>T maps to NM_014644.4 Q1195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:144857654 G>T maps to NM_014644.4 S2133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr4:120527914 C>T maps to NM_001083.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:149247705 G>A maps to NM_000440.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:149264055 G>A maps to NM_000440.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:648638 C>T maps to NM_000283.3 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:628554 C>T maps to NM_000283.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:650772 C>T maps to NM_000283.3 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr10:95399904 T>C maps to NM_006204.3 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr2:232601991 G>A maps to NM_002601.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:66753716 T>C maps to ENST00000401827 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr21:44190854 G>T maps to NM_002606.2 E545*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr22:39626110 C>T maps to NM_002608.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F5-01A-11D-A33T-08 chr22:39627770 G>A maps to NM_002608.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr11:103870918 G>A maps to NM_025208.4 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WL-01A-11D-A41K-08 chr11:104034550 G>A maps to NM_025208.4 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:55127502 G>A maps to NM_006206.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B2-01A-12D-A32B-08 chr5:149502717 C>T maps to NM_002609.3 V690V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr5:149497215 G>A maps to NM_002609.3 D1034D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr8:17447025 G>A maps to NM_006207.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:19369471 G>A did not map to a codon.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr4:96762204 C>T maps to NM_005390.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:335184 G>A maps to NM_006849.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr7:148701023 G>A maps to NM_004911.4 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:148701134 G>A maps to NM_004911.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:122811250 G>A maps to NM_006810.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr2:10929047 A>T maps to ENST00000381611 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr1:26449049 T>C maps to NM_152835.3 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:20370790 C>T maps to NM_174924.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:24516990 C>T did not map to a codon.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr4:95508145 G>A maps to NM_001011515.1 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176911073 G>A maps to NM_005451.3 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr1:13940849 C>T maps to NM_006474.4 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr16:70164410 G>A maps to NM_017990.3 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:70190673 C>T maps to NM_017990.3 I844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:32090465 G>A maps to NM_178140.2 T2304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr5:32089031 T>C maps to NM_178140.2 P1826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr5:32089964 A>G maps to NM_178140.2 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr5:32089673 G>A maps to NM_178140.2 A2040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr23:153073954 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr3:73450102 C>T maps to NM_015009.1 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:73433349 C>T maps to NM_015009.1 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:73433544 G>A maps to NM_015009.1 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:73433742 G>A maps to NM_015009.1 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:73657796 C>T maps to NM_015009.1 R254R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:160182918 G>A maps to ENST00000368075 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:156877419 C>T maps to NM_001080471.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr1:156883722 G>T maps to NM_001080471.1 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22584730 G>A maps to NM_144962.2 G120G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KK-A8IA-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr19:57326530 G>A maps to NM_006210.2 D1093D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:17412830 C>T maps to NM_148172.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:8049393 T>C maps to NM_002616.2 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr2:239160326 C>A maps to NM_022817.2 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:239167145 G>A maps to NM_022817.2 S589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr2:239160291 C>A maps to NM_022817.2 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:138413379 T>C maps to NM_022121.4 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:92147135 G>A maps to NM_000466.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:92146658 T>C maps to NM_000466.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:2340271 G>A maps to NM_153818.1 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:45937358 C>T maps to NM_057174.2 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr8:77895774 G>A maps to NM_001172087.1 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr6:143780271 G>T maps to NM_003630.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr3:179605497 C>T maps to NM_016559.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:137191047 G>A maps to NM_000288.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr23:54989708 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr23:54989722 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:48559454 G>A maps to NM_004567.2 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:48536608 G>A maps to NM_001166686.1 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:3124649 C>T maps to NM_002627.3 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:3146001 C>T maps to NM_002627.3 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr10:3177926 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44104759 C>T maps to NM_000290.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr23:77225015 G>A did not map to a codon.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:37830250 G>A maps to NM_033419.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:41704631 G>A maps to NM_002630.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr6:49754848 G>A maps to NM_138733.4 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr19:15582852 C>T maps to NM_052890.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:15580622 G>A maps to NM_052890.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr1:153314145 G>A maps to NM_020393.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr1:64104430 G>A maps to NM_002633.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:74053511 C>T maps to NM_173582.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr1:28764898 G>T maps to NM_023923.3 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr5:125936737 G>A maps to NM_032177.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:170105318 G>A maps to NM_018288.3 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:11030334 G>A maps to ENST00000303905 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr5:133914475 G>A maps to ENST00000448712 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:46887490 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr23:46913788 G>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:34389528 T>G did not map to a codon.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:34458922 A>G maps to NM_016436.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr6:64404529 G>A maps to NM_015153.2 Q852Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr6:64394234 C>T maps to NM_015153.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr23:54029073 A>C did not map to a codon.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr6:79672823 C>T maps to NM_017934.5 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr23:71840633 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:71800949 C>T did not map to a codon.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr23:18929060 G>A did not map to a codon.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:18912455 C>T did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr16:47533727 C>T maps to NM_000293.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr11:118516356 C>T maps to NM_015157.2 D1135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr11:118514552 C>T maps to NM_015157.2 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:71683233 C>T maps to NM_015020.2 R1177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:607295 C>A maps to ENST00000264555 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr7:77567151 C>T maps to ENST00000427986 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr10:13336426 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22079189 C>T maps to NM_014759.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr10:60994190 T>C maps to NM_032439.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:36931338 C>T maps to NM_153370.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr10:99426204 C>G maps to ENST00000416867 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:21174144 C>T maps to NM_058004.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr22:21097022 G>T maps to NM_058004.2 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr22:21167789 G>A maps to NM_058004.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:151278674 C>T maps to NM_002651.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:145578060 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr13:73396006 A>G maps to NM_006346.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr22:38468598 T>A maps to NM_012407.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:229890758 T>A maps to NM_017933.4 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:229890686 G>A maps to NM_017933.4 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr23:15342938 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35091338 G>A maps to NM_032634.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:624508 C>T maps to NM_148920.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr20:44054315 C>A maps to NM_015937.4 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:34893858 C>T maps to NM_178517.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr3:196460769 A>G maps to NM_001166304.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49950632 C>A maps to NM_017916.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49954060 C>T maps to NM_017916.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr10:98386516 G>A maps to NM_152309.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:204409440 G>A maps to NM_002646.3 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:204403685 G>A maps to NM_002646.3 Y1189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:18552760 T>C maps to NM_004570.4 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr18:39607409 T>C maps to ENST00000398870 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:178952025 C>A maps to NM_006218.2 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr3:178952049 T>G maps to NM_006218.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr1:9784113 G>A maps to ENST00000361110 R918R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:9775774 C>T maps to ENST00000361110 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:9781511 C>T maps to ENST00000361110 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr7:106509964 C>T maps to NM_002649.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr7:106513198 T>C maps to NM_002649.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr7:106508995 G>T maps to NM_002649.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18279700 C>T maps to NM_005027.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr19:18273221 G>T maps to NM_005027.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:46527680 C>T maps to NM_001114172.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:130452641 T>C maps to NM_014602.2 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:130463753 C>T maps to NM_014602.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:8792522 C>T maps to NM_001142633.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:8731969 G>A maps to NM_001010855.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr2:209190766 C>T maps to NM_015040.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:209167058 G>A maps to NM_015040.3 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99971946 G>A maps to NM_013439.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:22830862 G>A maps to NM_005028.4 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:36936737 C>T maps to NM_003559.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr12:57994721 C>T maps to NM_024779.4 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:3643242 G>A maps to NM_012398.2 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr19:3653332 G>A maps to NM_012398.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr19:3643248 C>T maps to NM_012398.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FU-01A-11D-A364-08 chr9:130688197 G>A maps to NM_001135219.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67260512 G>A maps to NM_004910.2 A1121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67265030 G>A maps to NM_004910.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67267629 G>A maps to NM_004910.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67270020 G>A maps to NM_004910.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:6381354 C>T maps to NM_031220.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:3208439 C>T maps to ENST00000380989 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:111539337 C>T maps to NM_153426.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:103990273 T>C maps to NM_005029.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:130839527 C>T maps to NM_004764.4 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:130827192 G>A maps to NM_004764.4 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:22140591 A>G maps to NM_001135721.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr22:25147434 A>G maps to NM_001008496.2 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:68381891 G>A did not map to a codon.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr16:2142145 C>T maps to NM_001009944.2 S3771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr16:2161024 G>A maps to NM_001009944.2 G1381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2160655 G>A maps to NM_001009944.2 D1504D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:47955074 T>C maps to NM_138295.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:47955196 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:81236212 C>T maps to NM_052892.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr10:102048746 G>A maps to NM_016112.2 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr22:46658214 G>T maps to NM_006071.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:46657944 G>A maps to NM_006071.1 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:46658025 G>T maps to NM_006071.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:51524057 G>A maps to NM_138694.3 C3622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:51915070 C>T maps to NM_138694.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr8:110420308 T>A maps to ENST00000426474 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr8:110495237 T>C maps to ENST00000426474 L3160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:110509271 C>T maps to ENST00000426474 C3484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr8:110420366 G>T maps to ENST00000426474 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr15:72502197 G>A maps to ENST00000419739 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:89236100 C>T maps to NM_006256.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:89250334 T>C maps to NM_006256.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:131482743 G>A maps to NM_013355.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr21:44427674 T>C maps to NM_004571.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr21:44433258 C>T maps to NM_004571.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:201292199 G>A maps to NM_000299.3 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr11:396953 C>G maps to NM_007183.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr10:74714238 G>A maps to NM_032562.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:68293283 G>A maps to NM_012320.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:31534278 C>T maps to NM_015715.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr1:186915808 A>G maps to NM_024420.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr1:186925323 C>G maps to NM_024420.2 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:42363729 G>A maps to NM_178034.3 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr15:42279574 T>G did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr15:42446633 C>T maps to ENST00000397272 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38522376 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr4:84015881 G>T maps to NM_001130715.1 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:84026087 G>A maps to NM_001130715.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:30784254 C>T maps to NM_002657.3 *497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:30785231 G>A maps to NM_002657.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr8:42045028 C>A maps to NM_000930.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:42040325 C>T maps to NM_000930.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:28761154 A>C maps to NM_001170585.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr2:28821555 C>T maps to NM_153021.4 Y801Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr12:113822715 C>G maps to NM_173542.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr12:113825599 C>G maps to NM_173542.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr20:9416221 T>G maps to NM_001172646.1 L847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:96058385 C>T maps to ENST00000371380 L1806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr10:95993810 G>A maps to ENST00000371380 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr16:81944187 C>T maps to NM_002661.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:81960740 C>T maps to NM_002661.2 V824V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr16:81891937 G>A maps to NM_002661.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr3:155206587 G>A maps to ENST00000340059 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:155199254 G>A maps to ENST00000340059 G1528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:155232631 C>T maps to ENST00000340059 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:2419085 C>A maps to NM_014638.2 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:17052133 G>A maps to NM_001144382.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr23:215817 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:207433 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:111426771 G>T did not map to a codon.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:18858170 G>A maps to ENST00000266505 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr8:144995012 G>T maps to NM_201380.2 I3129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr8:144998993 C>T maps to NM_201380.2 A1838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:145006672 G>A maps to NM_201380.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr8:144990641 C>G maps to NM_201380.2 A4586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:49363680 G>A maps to NM_020904.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49362847 G>A maps to NM_020904.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr12:19436439 C>T maps to ENST00000429027 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:30094418 G>A maps to ENST00000440706 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr19:30165018 G>A maps to ENST00000436066 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr6:151054999 G>A maps to NM_001029884.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr14:65194558 C>T maps to ENST00000394691 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr5:173067 C>T maps to NM_052909.3 C1013C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr5:162059 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr5:161983 C>T maps to NM_052909.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr17:40822620 G>A maps to NM_024927.4 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:40825730 C>T maps to NM_024927.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:43531225 G>A maps to NM_014798.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16046305 C>T maps to ENST00000420314 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16053820 C>T maps to ENST00000420314 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:909721 C>T maps to ENST00000379409 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:161134080 C>T maps to NM_000301.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:161160102 C>T maps to NM_000301.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:4523866 G>A maps to NM_001013706.2 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:23700885 G>A maps to NM_005030.3 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:57751418 G>A maps to NM_006622.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:57753105 G>A maps to NM_006622.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr4:128818020 G>T maps to NM_014264.4 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:128812836 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:12017969 C>T maps to ENST00000376369 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:12017930 G>A maps to ENST00000376369 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:103045509 G>A did not map to a codon.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr3:142396939 G>A maps to NM_001172312.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr3:146246433 T>C maps to NM_021105.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:146167019 G>A maps to ENST00000497985 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr3:146307580 C>T maps to NM_001085420.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:37234283 G>A maps to NM_020405.4 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr17:37243902 G>A maps to NM_020405.4 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr3:126748889 C>A maps to NM_032242.3 R1682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:126723742 C>T maps to NM_032242.3 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:126740950 G>A maps to NM_032242.3 S1354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:208390532 G>A maps to NM_025179.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:208215585 G>A maps to NM_025179.3 R1381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr23:153696268 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153689977 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153694315 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153696473 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr7:132192945 G>C maps to NM_020911.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:48461153 G>A maps to NM_001130082.1 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr22:50716551 T>C maps to NM_012401.2 S1627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr22:50720453 C>G maps to NM_012401.2 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr23:153039435 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:153033810 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153035309 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153043065 G>A did not map to a codon.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr3:129279277 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr3:129290378 G>A maps to NM_015103.2 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:56227285 C>T maps to NM_020182.3 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr1:156203418 G>T maps to NM_007221.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:72157463 G>A maps to NM_031293.2 Q892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr7:102944391 C>T maps to NM_004279.2 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:152937470 A>G did not map to a codon.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr19:50370407 T>C maps to NM_007254.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:160237000 T>C maps to NM_173516.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr10:118320019 C>T maps to NM_000936.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:118313342 C>T maps to NM_000936.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr10:118357364 C>T maps to NM_006229.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:118228728 C>T maps to NM_001011709.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:26365434 C>T maps to NM_007257.5 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr8:26366212 G>T maps to NM_007257.5 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr23:152158950 T>G did not map to a codon.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr19:46997771 C>T maps to NM_020709.1 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:46997591 G>A maps to NM_020709.1 S377S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr14:20942984 C>T maps to NM_000270.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr6:36270247 T>C did not map to a codon.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr23:7880087 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:7606906 G>A maps to NM_001166111.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr9:140392627 G>A maps to NM_001098537.1 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:140361840 G>T maps to NM_001098537.1 A989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OY-01A-11D-A41K-08 chr19:14043544 G>A maps to NM_024825.3 H504H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:127388015 C>T maps to NM_015720.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr23:84561265 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:151396573 G>A maps to NM_015100.3 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:151396579 G>A maps to NM_015100.3 N456N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:151396612 T>C maps to NM_015100.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr23:24861701 A>G did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:50905528 C>T maps to ENST00000391817 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr11:74303720 T>G maps to NM_006591.1 Y6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr17:26680001 G>A maps to NM_015584.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr22:42981904 G>A maps to ENST00000415122 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr12:133249851 C>T maps to ENST00000455752 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:133209373 G>A maps to ENST00000455752 I2007I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:133244172 G>T maps to ENST00000455752 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr15:89871739 G>A maps to NM_002693.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:89866118 A>G maps to NM_002693.2 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:62492846 A>G maps to NM_007215.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr3:121208387 A>G maps to ENST00000393672 N1266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:121251941 G>A maps to ENST00000393672 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr3:121228542 C>A maps to ENST00000393672 V744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:86304987 A>G maps to NM_015425.3 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:57876616 A>C maps to NM_000938.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr4:57876597 C>T maps to NM_000938.1 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:57860572 C>T maps to NM_000938.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38352842 C>T maps to ENST00000407936 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:106838327 G>A maps to NM_018082.5 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:106770184 G>A maps to NM_018082.5 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:106827516 C>T maps to NM_018082.5 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr8:22105703 A>G maps to NM_001722.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:18464141 C>T maps to NM_006466.2 H297H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:621234 C>T maps to NM_005035.3 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr7:72400573 T>G maps to ENST00000434423 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:75053836 C>T maps to ENST00000257665 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:46661563 C>T maps to ENST00000371986 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr13:29242674 G>A maps to NM_015932.5 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr13:38138689 G>A maps to NM_006475.2 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr13:38159065 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:43147833 C>G maps to NM_001005365.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr2:131976469 C>T maps to NM_001083538.1 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:131976049 C>T maps to NM_001083538.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr2:131976100 C>T maps to NM_001083538.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:87325525 G>A maps to NM_001122757.1 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:111228346 C>T maps to NM_006235.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:111225282 C>T maps to NM_006235.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr19:42597984 T>C maps to ENST00000342301 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr23:82763399 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:82764213 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:79176629 C>T maps to NM_006237.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr4:147561254 C>T maps to NM_004575.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:128428779 A>C maps to NM_001159542.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr8:128428374 C>T maps to NM_001159542.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr8:128428596 T>G maps to NM_001159542.1 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:93077200 C>T maps to NM_153216.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr7:39500236 T>A maps to NM_007252.3 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr5:54771250 G>T maps to NM_003711.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr9:134183364 C>T maps to NM_032728.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr9:134165680 C>T maps to NM_032728.3 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr9:134165482 G>A maps to NM_032728.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr4:23815647 G>A maps to NM_013261.3 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr4:23886555 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:23830128 G>A maps to NM_013261.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr5:149212574 C>G maps to NM_133263.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:149212310 C>T maps to NM_133263.3 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:149216273 C>T maps to NM_133263.3 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr4:57272693 G>A maps to NM_002703.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr23:18842130 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr4:76813114 G>A maps to NM_006239.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr19:49653358 G>C maps to NM_003660.2 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr19:49633699 C>T maps to NM_003660.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:27835612 C>T maps to NM_003622.3 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:7673018 C>T maps to NM_003621.2 R794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:40209538 G>A maps to NM_006112.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr2:170493057 A>G maps to NM_004792.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr2:170493493 C>T maps to NM_004792.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:22039093 C>T maps to NM_148175.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:149826609 T>C maps to NM_139126.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:149826636 G>A maps to NM_139126.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:149833428 G>A maps to NM_139126.2 Y363Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:43827081 G>A maps to NM_001130858.2 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr5:102484975 C>T maps to ENST00000451606 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:102487000 C>A maps to ENST00000451606 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr14:60749575 C>A maps to NM_177952.2 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:58700882 G>A maps to NM_003620.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr1:161140215 G>A maps to NM_001122764.1 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:161137270 C>T maps to NM_001122764.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr19:55603824 G>A maps to NM_017607.2 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr14:104212713 T>C maps to NM_015316.2 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr14:104251153 G>A maps to NM_015316.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:104206283 G>A maps to NM_015316.2 N823N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:104219353 G>A maps to NM_015316.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:45888874 G>A maps to NM_001142502.1 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr6:150569955 A>C maps to NM_030949.2 *166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:145722825 C>T maps to NM_032902.5 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr8:145726658 C>T maps to NM_032902.5 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr8:145726590 C>T maps to NM_032902.5 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr12:54974736 T>C maps to NM_006741.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr17:37792096 C>A maps to ENST00000394271 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:37791875 C>A maps to ENST00000394271 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr7:113518487 C>A maps to NM_002711.3 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr7:113519778 G>C maps to NM_002711.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:113519010 T>C maps to NM_002711.3 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:113558763 C>T maps to NM_002711.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr7:113519340 A>G maps to NM_002711.3 H602H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr20:58514329 C>T maps to NM_006242.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:49142940 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:94898625 G>A maps to NM_001166160.1 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:94750099 C>T maps to NM_001166160.1 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr17:48216859 C>T maps to NM_032595.3 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr19:52723056 C>T maps to NM_014225.5 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:26227724 A>G maps to NM_001177591.1 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr5:146080670 C>T maps to ENST00000394414 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr5:146080618 G>A maps to ENST00000394414 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:133769187 C>T maps to ENST00000455566 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr3:135722331 C>T maps to NM_002718.4 I664I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr11:64694284 G>T maps to NM_006244.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr14:102391491 G>A maps to NM_002719.3 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:42975222 C>T maps to NM_006245.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22398278 G>A maps to ENST00000397775 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:9559584 C>T maps to NM_001042388.1 A620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:9588807 G>A maps to NM_001042388.1 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:73096417 G>A maps to NM_174907.2 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:46857143 G>A maps to NM_006247.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:127916000 C>T maps to NM_001123355.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:32122415 G>A maps to NM_138717.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:47087265 G>A maps to NM_005972.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:11317935 C>T maps to NM_152391.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr1:12854345 G>A maps to NM_023013.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr1:12884844 G>A maps to NM_001146344.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr1:12887307 C>T maps to NM_001146344.1 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr1:12887676 A>G maps to NM_001146344.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OF-01A-11D-A41K-08 chr1:13695959 G>T maps to NM_001099850.1 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr1:12943194 A>G maps to NM_001009611.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr12:11461247 C>T maps to NM_002723.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr15:91524743 T>C maps to NM_003981.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr15:91513729 G>T maps to NM_003981.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156737868 G>A maps to NM_005973.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156764467 G>A maps to NM_005973.4 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr11:82560219 G>A maps to NM_199418.2 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:129800949 C>T maps to NM_020228.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr11:129807532 C>A maps to NM_020228.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr8:70978695 T>C maps to NM_024504.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:43282054 G>A maps to NM_022115.3 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:3328641 C>T maps to NM_022114.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:3328821 C>T maps to NM_022114.3 G687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr1:14108528 G>C maps to NM_012231.4 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr4:81123236 C>T maps to NM_001099403.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:81123530 C>A maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:81123566 G>A maps to NM_001099403.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr4:81123236 C>T maps to NM_001099403.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NJ-01A-22D-A34U-08 chr5:23526963 T>C maps to NM_020227.2 F589F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:23522810 G>A maps to NM_020227.2 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:23527521 C>A maps to NM_020227.2 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:105781267 G>A maps to NM_002726.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr8:69046378 G>A maps to NM_024870.2 A1284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:69002946 G>A maps to NM_024870.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr10:72358720 G>A maps to NM_005041.4 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr10:72358339 C>T maps to NM_005041.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:11083322 C>T maps to NM_001110213.1 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr13:28562732 G>A maps to NM_001105577.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr20:62196337 C>T maps to NM_001037335.2 P1279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr3:64084857 G>A maps to NM_198859.3 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:64085458 G>A maps to NM_198859.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:57246842 T>C maps to NM_000947.2 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:57161694 G>A maps to NM_006252.3 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr12:120110137 G>A maps to NM_006253.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:14204547 C>A maps to NM_002730.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:14208432 G>A maps to NM_002730.3 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:71628978 G>A maps to NM_002732.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:71628906 G>A maps to NM_002732.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr7:151273532 T>C maps to NM_016203.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr17:66519942 T>C maps to NM_212472.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:64641528 C>T maps to NM_002737.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:64728819 C>T maps to NM_002737.2 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:23999907 C>T maps to NM_002738.6 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr19:54395834 C>T maps to NM_002739.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:61924007 C>T maps to NM_006255.3 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr10:6539185 G>A maps to NM_006257.2 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr19:11558390 G>A maps to ENST00000436195 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:2116390 G>A maps to NM_002744.4 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:47219513 G>A maps to ENST00000449438 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr8:48776072 C>A maps to NM_006904.6 V1878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr4:82064094 G>A maps to NM_006259.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr23:3573440 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:3592734 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:22290545 G>A maps to ENST00000397199 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr11:20409623 G>T maps to NM_005788.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr11:20424496 C>T maps to NM_005788.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr14:23395505 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:107600026 C>T maps to NM_018137.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:4680519 C>T maps to NM_001080123.1 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:128186434 C>T maps to ENST00000409048 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:68882251 G>T maps to NM_138964.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:68882131 C>T maps to NM_138964.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:68882257 C>T maps to NM_138964.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr20:5283270 G>T maps to NM_144773.2 Y190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr4:16019993 G>A maps to NM_006017.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr4:16026832 G>A maps to NM_006017.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:177419760 T>G maps to NM_006261.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr5:177419967 G>A maps to NM_006261.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:93624976 G>A maps to NM_000313.3 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr8:37623075 G>A maps to NM_007198.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr1:214171236 C>T maps to NM_002763.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr14:75329861 G>A maps to ENST00000445876 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr10:13642287 T>C maps to NM_003675.3 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr10:13658528 C>T maps to NM_003675.3 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr11:60666068 C>A maps to NM_014502.4 G362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr11:60658694 G>A maps to NM_014502.4 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:150297486 G>A maps to NM_004698.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr19:54627953 G>A maps to NM_015629.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:116045693 C>T maps to NM_004697.3 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:50037896 G>A maps to NM_001031698.1 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr17:1563821 G>A maps to NM_006445.3 H1563H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:1577959 C>T maps to NM_006445.3 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:1585166 G>A maps to NM_006445.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:18067045 A>G maps to NM_175886.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:57247184 C>A maps to NM_018304.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50097975 G>T maps to NM_020719.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr19:50123645 G>A maps to NM_020719.1 A1845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:120022391 T>C maps to NM_016644.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:5784047 T>C maps to NM_001134316.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr6:30525975 C>T maps to NM_025263.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr22:45128195 G>C maps to ENST00000352766 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:45182349 C>T maps to ENST00000352766 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:36472797 C>T maps to NM_001160167.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr23:37285149 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:150869493 G>A did not map to a codon.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr3:9990881 C>T maps to NM_207351.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:119234368 G>A maps to NM_003619.3 H492H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:2903246 G>A maps to NM_022119.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr16:2770146 C>T maps to NM_031948.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2764111 C>T maps to NM_031948.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr16:58314535 G>A maps to NM_001080492.1 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr10:25160953 G>A maps to NM_020200.5 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr15:55964736 C>T maps to NM_173814.4 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:55930777 G>A maps to NM_173814.4 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:55930825 G>A maps to NM_173814.4 Y791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:55970052 C>T maps to NM_173814.4 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr9:79322278 T>C maps to NM_015225.2 L1637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr19:40901384 C>T maps to NM_181882.2 K958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr19:40903196 G>A maps to NM_181882.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:80915564 C>T maps to ENST00000421149 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr9:80923473 T>C maps to ENST00000421149 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:143762787 C>T maps to ENST00000301258 N32N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:139201585 G>A maps to NM_032289.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr2:113958985 G>A maps to NM_012455.2 Q1055Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:227083145 C>T maps to ENST00000391872 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr19:43519266 C>A did not map to a codon.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr19:43233350 G>A maps to NM_021016.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:43233461 C>T maps to NM_021016.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr19:43244509 G>A maps to NM_021016.3 C9C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr19:43702386 A>G maps to NM_002780.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr19:43411266 G>A maps to NM_002782.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr19:43439763 G>A maps to NM_002783.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:78838014 G>A maps to NM_002789.4 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr18:23759095 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:36101916 G>A maps to NM_002794.4 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr1:151372580 C>T maps to NM_002796.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:53185070 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:65343565 T>C maps to NM_002816.3 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr16:74336162 G>A maps to NM_002811.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr18:12706676 G>T maps to NM_020232.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr19:804111 G>T maps to NM_002819.4 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:804674 C>T maps to NM_002819.4 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr1:45296669 C>T maps to NM_003738.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr1:45295345 A>T maps to NM_003738.4 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr23:23397962 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr1:11596382 C>T maps to NM_020780.1 D1273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr10:27702747 C>T maps to NM_001034842.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr10:27702369 G>A maps to NM_001034842.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr10:27702555 G>A maps to NM_001034842.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:97312001 C>T maps to NM_014754.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:89690801 G>A did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr10:89692848 G>A maps to NM_000314.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr14:52735164 C>T maps to NM_000953.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr9:139874416 C>T maps to ENST00000224167 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:52781865 C>T maps to NM_000956.3 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:40681889 C>T maps to NM_000958.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:40691948 G>A maps to NM_000958.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr1:78959036 A>C maps to NM_000959.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr1:117484586 C>T maps to NM_020440.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr20:48166724 G>A maps to NM_000961.3 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:125154675 C>T maps to NM_000962.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:46945058 C>T maps to NM_000316.2 N565N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr3:46944115 C>T maps to NM_000316.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:209302259 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr2:209358095 G>T maps to NM_005048.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr2:209307105 C>T maps to NM_005048.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr2:209345820 G>A maps to NM_005048.2 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:141754811 G>A maps to NM_005607.4 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:141856768 G>A maps to NM_005607.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:27310661 G>A maps to NM_004103.3 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:62163963 C>T maps to NM_005975.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:43109738 C>T maps to NM_002821.3 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr7:136936040 G>A maps to NM_002825.5 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr9:96860385 C>G maps to ENST00000434261 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr10:17645743 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:49191124 A>G maps to NM_002827.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr7:77256289 C>T maps to NM_002835.3 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:131116854 C>T maps to NM_014369.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr14:88945893 C>T maps to NM_007039.3 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:88946187 C>T maps to NM_007039.3 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr14:89016641 G>A maps to NM_007039.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:114401161 G>A maps to NM_015967.5 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr3:47450482 C>T maps to NM_015466.2 H516H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr3:47437634 T>C maps to NM_015466.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:112185101 C>T maps to NM_002829.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:112145795 G>A maps to NM_002829.3 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr11:18762158 C>T maps to NM_032781.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:7061280 C>T maps to ENST00000416215 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:202128421 G>A maps to ENST00000309017 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr15:75798218 G>A maps to NM_002833.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr15:75819590 C>T maps to NM_002833.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr12:70925904 G>A maps to NM_001109754.1 I2138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:198719700 C>T maps to ENST00000271610 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:198711450 T>C maps to ENST00000271610 Y884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr1:198704260 G>A maps to ENST00000271610 K761K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr9:8317915 G>A maps to NM_002839.3 A1899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr9:8636727 C>A maps to NM_002839.3 G61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:8404588 G>A maps to NM_002839.3 Y1386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IC-01A-11D-A364-08 chr10:129854463 C>T maps to NM_006504.4 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:129877926 C>T maps to NM_006504.4 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:62253391 C>T maps to NM_002841.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr19:55711745 G>A maps to NM_002842.3 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr19:55699454 G>A maps to NM_002842.3 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:48161137 G>A maps to NM_002843.3 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OF-01A-11D-A41K-08 chr11:48145256 C>A maps to NM_002843.3 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr6:128294292 G>A maps to ENST00000368210 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr18:8113636 C>A maps to NM_001105244.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:8387203 C>T maps to NM_001105244.1 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:220161052 G>A maps to NM_002846.3 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr7:157931052 C>T maps to NM_002847.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr12:15710428 G>T maps to NM_030667.1 E867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr12:15742394 C>T maps to NM_030667.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:15669886 C>T maps to NM_030667.1 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:5274308 C>T maps to NM_002850.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:5245856 C>T maps to NM_002850.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:5214706 G>A maps to NM_002850.3 D1453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:5208350 G>A maps to NM_002850.3 Q1847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr1:29638246 C>T maps to NM_005704.4 V1026V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr7:121652282 G>A maps to NM_002851.2 E1061E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr7:121651646 C>T maps to NM_002851.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:121651337 G>A maps to NM_002851.2 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:121652879 G>A maps to NM_002851.2 L1260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:40557265 G>A maps to NM_012232.5 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr17:40557271 C>T maps to NM_012232.5 S202S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-QU-A6IO-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:159854761 G>A maps to NM_004219.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr3:157154781 G>A maps to NM_002852.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S0-01A-11D-A41K-08 chr3:157154852 G>A did not map to a codon.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr16:1537737 C>T maps to NM_001013658.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:1536524 G>A maps to NM_001013658.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:20463105 A>C maps to ENST00000361078 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:61175176 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:37211238 G>A maps to NM_002854.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr3:110845028 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:110852710 G>A maps to NM_015480.1 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:134218870 C>T maps to NM_138499.3 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:134218981 G>A maps to NM_138499.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr8:52320733 G>T maps to NM_144651.4 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr8:52359717 C>A maps to NM_144651.4 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr8:52321582 G>A maps to NM_144651.4 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr8:52336237 C>T maps to NM_144651.4 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr16:31213082 G>A maps to NM_013258.4 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:226109029 G>A maps to NM_013328.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:31228334 G>A maps to NM_152901.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr14:51383368 G>C maps to NM_002863.4 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr14:51376764 C>A maps to NM_002863.4 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64519437 G>A maps to NM_005609.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:100144809 G>A maps to NM_032709.2 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr10:100152746 C>T maps to NM_032709.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr3:49136842 G>A maps to NM_005051.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr6:163899928 G>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:29708605 C>T maps to NM_014298.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr4:122250474 C>T maps to NM_198179.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74286132 C>T maps to NM_032134.1 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr2:136481597 C>T maps to ENST00000409606 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:136418856 C>T maps to ENST00000409606 C648C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr12:57674221 C>T maps to ENST00000438036 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:8464807 C>T maps to NM_004218.3 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:37730603 G>A maps to NM_001002814.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr8:37732085 C>T maps to NM_001002814.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr16:570796 G>A maps to NM_014700.3 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:29761109 C>T maps to NM_032932.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr2:73316400 T>C maps to NM_015470.2 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr1:153958655 C>T maps to NM_002870.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:65417800 G>A maps to NM_198686.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr14:65417800 G>A maps to NM_198686.2 D105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:238494710 G>A maps to NM_022449.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr5:176728924 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176729461 G>A maps to NM_130781.2 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156038133 C>T maps to NM_020387.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr23:129318353 C>T did not map to a codon.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr4:140393994 T>C maps to NM_031296.1 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr17:72736965 C>T maps to NM_001006638.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:72736965 C>T maps to NM_001006638.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr11:107832735 C>T maps to NM_017516.1 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:107832959 G>A maps to NM_017516.1 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:154490315 G>A did not map to a codon.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:18313412 C>T maps to NM_002866.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr5:57913606 C>T maps to NM_138453.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:11447928 G>A maps to NM_004283.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:135893243 G>A maps to NM_001172435.1 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:135908033 C>T maps to NM_001172435.1 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:220363469 T>C maps to ENST00000358951 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr1:229431651 C>T maps to NM_004578.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr2:130738002 A>G maps to NM_032144.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr2:130738443 G>C maps to NM_032144.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:13727113 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:5264855 A>G maps to NM_004703.4 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr17:5264970 G>C did not map to a codon.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr9:125860017 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:68670492 C>T maps to NM_133339.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:117878923 G>A maps to NM_006265.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr8:117859876 T>G maps to NM_006265.2 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:41020959 G>A maps to NM_002875.4 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr8:95403997 G>A maps to NM_012415.2 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:110960162 G>T maps to NM_152442.3 E358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr7:4874798 G>A maps to NM_018059.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:4856947 C>T maps to NM_018059.4 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:4917278 G>A maps to NM_018059.4 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr7:4876195 C>T maps to NM_018059.4 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:55948749 C>T maps to NM_001015885.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:150239452 G>A maps to NM_001001788.2 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr3:12632412 T>G maps to ENST00000415519 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:12653483 G>A maps to ENST00000415519 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:36615226 A>G maps to NM_000536.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr11:36615349 G>T maps to NM_000536.3 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:17699168 C>T maps to ENST00000395776 D969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:34826504 C>G maps to NM_001145521.1 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:34811224 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:34814746 G>A maps to NM_001145521.1 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr18:9522267 C>T maps to NM_006788.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr18:9524698 G>A maps to NM_006788.3 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr14:36039875 T>G maps to NM_194301.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr20:20592030 A>G maps to NM_020343.3 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr20:20517345 G>T maps to NM_020343.3 S1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr20:37144918 G>A maps to NM_020336.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:129931000 C>T maps to NM_014636.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:129974997 C>T maps to NM_014636.2 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr8:85799875 G>T maps to NM_001100391.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:85441792 C>G maps to NM_001100391.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr7:45222941 C>T maps to NM_005856.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:170669732 C>T maps to NM_022897.3 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:170725810 G>A maps to NM_022897.3 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:170640637 C>T maps to NM_022897.3 Y745Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:109365451 C>T maps to NM_006267.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:109371408 C>T maps to NM_006267.4 Q751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:5933452 C>T maps to NM_007322.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr9:6013360 A>T maps to NM_012416.2 Y749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr9:6015580 C>A maps to NM_012416.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr6:13625975 T>C maps to NM_005493.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr6:13697084 C>T maps to NM_005493.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:69044217 C>T maps to NM_015646.4 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:21935360 C>T maps to NM_001145658.1 E444E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:134497350 C>T maps to NM_198679.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:173852993 C>T maps to NM_007023.3 Y407Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:130766662 G>A maps to ENST00000514667 Q1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr5:130766834 G>T maps to ENST00000514667 T1444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:88240651 T>C maps to NM_020320.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr6:88240516 G>A maps to NM_020320.3 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:141290328 C>T maps to ENST00000452898 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr13:114780694 C>T maps to ENST00000389544 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:17398528 C>T maps to NM_016084.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:179564989 G>A maps to NM_175062.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr5:179565028 G>A maps to NM_175062.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:79296192 G>A maps to NM_002891.4 G816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:80369157 C>T maps to NM_006909.1 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:80497208 C>T maps to NM_006909.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:33745724 C>T maps to NM_170672.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:33745673 T>C maps to NM_170672.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr20:4770304 G>A maps to NM_014737.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:26217738 G>T maps to NM_001164747.1 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:86198983 C>T maps to NM_005447.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr13:48941652 C>T maps to NM_000321.2 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:24574973 A>G maps to NM_006910.4 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:20562267 C>T maps to ENST00000360790 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:18470587 G>A maps to NM_006606.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr20:35668589 C>T maps to NM_002895.2 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr16:53485705 T>C maps to NM_005611.3 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr23:47039693 C>G did not map to a codon.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:47030609 A>G did not map to a codon.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr21:15592039 C>T maps to NM_144770.3 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr20:34240745 G>A maps to NM_001198838.1 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr20:34240453 A>G maps to NM_001198838.1 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr6:155131225 C>G maps to NM_014892.3 S435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr5:145641191 G>A maps to NM_018989.1 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:235301419 C>T maps to NM_015014.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr23:106312567 C>T did not map to a codon.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr23:106358622 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr2:238737874 T>C maps to NM_001080504.2 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66436507 G>A maps to NM_031492.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:50147120 G>A maps to NM_005778.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:50151654 C>T maps to NM_005778.2 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr3:50005400 T>C maps to NM_005777.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:36142521 G>A maps to NM_001082578.1 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr23:135961212 G>T did not map to a codon.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:89448491 T>G maps to NM_019610.5 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr1:89448492 G>A maps to NM_019610.5 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr11:7111256 C>T maps to NM_014469.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:7111073 C>T maps to NM_014469.4 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:48390796 C>A maps to NM_002900.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr10:48389851 C>T maps to NM_002900.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr10:48389893 C>G maps to NM_002900.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:26407824 C>T maps to NM_005349.2 R43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:43940961 T>C maps to NM_014276.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:30416411 G>A maps to NM_006867.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr15:65041629 G>A maps to NM_194272.1 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr15:65041628 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr1:24861592 T>C maps to NM_013441.2 Y184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr13:50123714 G>A maps to NM_018191.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:28858369 C>T maps to NM_001048194.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:9804387 G>A maps to NM_002903.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr12:57346015 C>A maps to NM_003708.3 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr17:34249536 T>G maps to NM_001034836.1 *237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:110124752 G>A maps to ENST00000405097 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr14:24642194 C>T maps to NM_005132.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:36087700 C>T maps to NM_021111.2 C216C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr12:21626536 T>C maps to NM_032941.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145737880 G>A maps to ENST00000428558 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:73627744 G>A maps to NM_004259.5 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr2:79349166 C>T maps to NM_002909.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:120342380 C>T maps to NM_032044.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr19:45525435 G>A maps to ENST00000221452 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:141017908 C>G maps to NM_173828.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr7:103341382 C>T maps to ENST00000428762 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:103191623 G>A maps to ENST00000428762 H2064H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:103244917 G>A maps to ENST00000428762 T1007T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:103322654 G>A maps to ENST00000428762 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:73103307 C>T maps to NM_152222.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:73105728 C>T maps to NM_152222.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr1:204128549 G>A maps to NM_000537.3 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr23:153208480 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:8424211 G>A maps to NM_012102.3 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:18237548 C>A maps to NM_024730.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:43597967 C>A maps to NM_020975.4 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:43622198 C>T maps to NM_020630.4 F1072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr2:100055180 C>T maps to NM_016316.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:111726772 C>T maps to NM_002912.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:1816552 C>T maps to NM_020695.3 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:118454652 G>A maps to NM_007370.4 K7K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:33344574 G>A maps to NM_001017368.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr6:112671563 C>A maps to NM_001013734.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A722-01A-12D-A364-08 chr3:53157856 C>G did not map to a codon.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr1:175996717 G>A maps to NM_022457.5 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr16:74670337 T>C maps to NM_018124.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr19:14083866 G>A maps to NM_002918.4 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr9:3293174 G>A maps to NM_134428.1 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:151316214 C>T maps to NM_000449.3 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr6:117245848 C>T maps to NM_173560.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr15:56386856 C>T maps to NM_022841.5 P1023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr19:19309476 G>A maps to NM_003721.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr13:37401781 G>A maps to NM_000538.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr13:37399673 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:109696268 G>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:71349789 C>T did not map to a codon.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr23:71351090 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:183853013 C>T maps to NM_015149.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:98128862 G>A maps to NM_001012761.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:86007449 G>A maps to ENST00000358110 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr16:321438 C>A maps to NM_183337.1 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:3318862 C>T maps to NM_198229.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:3430394 T>C maps to NM_198229.2 I1174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:192628556 C>T maps to NM_144766.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:54791831 A>T maps to NM_170587.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:101020623 C>T maps to NM_015668.3 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr9:116356366 C>G maps to NM_144489.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:163122354 C>T maps to NM_003617.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr14:72976880 C>T maps to NM_004296.4 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr14:73029173 G>C maps to NM_004296.4 *473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr1:240977012 C>A maps to ENST00000407727 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:241033417 G>A maps to ENST00000407727 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MF-01A-11D-A364-08 chr5:63890652 C>T maps to NM_001029875.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr17:63204084 C>T maps to NM_003835.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr19:33167291 A>G maps to NM_207391.2 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:227729678 G>A maps to NM_001167608.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:75511510 C>A maps to NM_001040456.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:114719 C>T maps to NM_022450.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:74467834 G>A maps to NM_024599.5 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:30625114 G>T maps to NM_138328.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr1:156347176 C>T maps to NM_020407.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:90019994 G>A maps to NM_016321.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:25617206 G>A maps to ENST00000357542 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr3:129251240 C>T maps to NM_000539.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:22862015 C>T maps to NM_001160036.1 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22862090 G>A maps to NM_001160036.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:22872263 C>T maps to NM_001160036.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:95091241 C>T maps to NM_014899.3 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr5:95067674 G>T maps to NM_014899.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:3849002 C>T maps to NM_001665.3 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr14:63671715 C>T maps to NM_020663.3 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr1:228871653 C>T maps to NM_021205.4 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr23:53455598 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:214298 C>T maps to NM_021932.4 C521C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr17:12847398 G>A maps to NM_014859.4 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:38945048 T>G maps to ENST00000296782 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr12:123915095 C>T maps to NM_145058.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr12:130926704 G>A maps to NM_015347.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:42880422 G>A maps to NM_173642.3 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:8906615 C>T maps to NM_020734.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:105001554 C>T maps to NM_001100117.2 R984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr1:41098807 G>A maps to NM_014747.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr6:3113515 C>T maps to NM_003804.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:3077074 C>A maps to NM_003804.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:3085631 G>A maps to NM_003804.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:43161903 C>T maps to ENST00000352483 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:40704480 T>A maps to NM_012421.3 C1369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr23:73811937 G>C did not map to a codon.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr23:73811347 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:5300247 T>C maps to NM_134441.1 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67681779 C>A maps to NM_001013838.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67683980 C>T maps to NM_001013838.1 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr9:86616311 G>T maps to NM_024945.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:151766708 G>A maps to NM_017909.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr14:21250157 C>T maps to NM_005615.4 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:182550488 G>A maps to NM_021133.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:182555275 C>T maps to NM_021133.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:31435892 C>T maps to NM_013235.4 Q1007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr12:120990387 T>G maps to ENST00000458409 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr23:119005302 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49735361 C>T maps to NM_022064.2 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:49753835 C>T maps to NM_022064.2 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:7160685 G>A maps to NM_014746.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr2:7179869 C>T maps to NM_014746.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:122342453 G>A maps to NM_198085.1 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr21:30354639 C>T maps to NM_015565.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr13:25348979 C>T maps to ENST00000381927 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr9:104314096 A>G maps to NM_019592.5 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr1:6279430 G>C maps to NM_207396.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:1067392 G>A maps to NM_001131034.3 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr17:78286954 C>T maps to NM_020914.4 V982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78265573 C>T maps to NM_020914.4 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78320609 C>T maps to NM_020914.4 C2874C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78349609 G>A maps to NM_020914.4 L4424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr11:117117566 G>T maps to NM_207343.2 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:30776080 C>T maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr7:5780783 A>C maps to NM_207111.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:5800646 G>A maps to NM_207111.2 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr1:44877960 C>T maps to ENST00000453887 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr7:156469180 C>T maps to NM_001184997.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:36351114 G>A maps to NM_022781.4 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:56435188 G>A maps to NM_017763.4 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr17:56439944 G>T maps to NM_017763.4 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr13:26788079 G>A maps to NM_005977.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:26793669 G>T maps to NM_005977.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:13737028 C>T maps to NM_003799.1 R192*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G9-7510-01A-11D-2260-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:201972552 C>T maps to NM_020216.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr3:78667055 C>T maps to NM_002941.3 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:77614126 C>T maps to ENST00000332191 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:77671485 C>T maps to ENST00000332191 A1221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr3:77147466 C>T maps to ENST00000332191 R122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:18533606 C>T maps to NM_005406.2 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:18562758 G>A maps to NM_005406.2 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:115024861 C>T maps to NM_001163790.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:94495689 C>T maps to NM_004560.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:94486291 C>T maps to NM_004560.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr15:60919519 C>T maps to NM_134260.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:117663707 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:117645560 C>A maps to NM_002944.2 E1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:117662660 G>A maps to NM_002944.2 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:117642474 C>T maps to NM_002944.2 E1908E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr8:55540710 T>A maps to NM_006269.1 C1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr8:55533942 C>G maps to NM_006269.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr8:55537425 C>T maps to NM_006269.1 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr8:55538976 G>A maps to NM_006269.1 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88N-01A-11D-A364-08 chr8:55540776 T>A maps to NM_006269.1 S1445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr8:10465052 T>A maps to NM_178857.5 A2185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr8:10468679 C>T maps to NM_178857.5 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr8:10470653 G>A maps to NM_178857.5 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr8:10468856 C>T maps to NM_178857.5 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr8:10470173 G>A maps to NM_178857.5 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr7:33138943 C>T maps to NM_203288.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:33136123 G>A maps to NM_203288.1 R150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr23:96140038 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr23:96140002 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:92789301 C>T maps to NM_024813.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:68906684 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:38147243 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:38178227 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:38182681 A>G did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr14:21796692 C>A maps to NM_020366.3 Y1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr14:21790126 G>T maps to NM_020366.3 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:53672317 A>C maps to NM_015272.2 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr12:113307698 C>A maps to NM_001143854.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:97004 G>A maps to NM_006987.3 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr23:153628937 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr6:35437257 G>T maps to NM_007104.4 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr6:35437187 T>A maps to NM_007104.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr3:23960790 C>T maps to NM_002948.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:17973015 C>T maps to NM_000980.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr3:52027887 G>A maps to NM_000992.2 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr16:1996980 G>A maps to NM_005061.2 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120635151 C>T maps to NM_053275.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:120637004 C>T maps to NM_053275.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:69747803 C>T maps to NM_001003.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr6:30314251 C>T maps to ENST00000412529 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr10:92655209 G>C did not map to a codon.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr10:92660333 A>G maps to ENST00000458617 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr10:15145357 G>A maps to NM_183005.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:15145384 G>A maps to NM_183005.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr20:36686046 G>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:150444463 A>T maps to NM_015203.3 K1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr16:2014491 G>A maps to NM_002952.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr24:22930772 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:166844000 G>A maps to ENST00000510118 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr23:20190905 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:20222194 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr23:83411184 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:58009015 G>A maps to NM_003161.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67201897 G>A maps to NM_003952.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr19:54710321 C>T maps to NM_001013.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr3:39450136 T>G maps to ENST00000443003 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:152127347 G>A maps to NM_001122965.1 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr1:152128185 A>G maps to NM_001122965.1 Y463Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr17:78857259 C>T maps to NM_020761.2 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr16:836243 G>A maps to NM_058192.2 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:55777597 G>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:39325294 C>T maps to NM_022157.2 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr19:50138859 G>T maps to NM_006270.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:17622554 T>A maps to ENST00000377813 K691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr6:7240689 T>A maps to NM_001003699.3 C1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:7230077 G>A maps to NM_001003699.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:110758736 G>A maps to NM_006583.2 W232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr11:4130908 C>T maps to NM_001033.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:99141222 G>A maps to NM_015179.3 C446C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:48557075 T>C maps to NM_018346.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:7018221 C>A maps to NM_080657.4 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:114308828 G>T maps to NM_018364.3 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:114310902 C>A maps to NM_018364.3 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:114354569 C>T maps to NM_018364.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr1:15986476 C>T maps to NM_006511.1 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:15987988 C>A maps to NM_006511.1 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:159403612 C>T maps to NM_031924.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:116949447 C>T maps to NM_001010892.2 N526N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:46299170 C>A maps to NM_030785.3 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr6:43623375 C>T maps to NM_152732.4 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:158015855 G>T maps to NM_016625.2 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr19:12940771 G>A maps to NM_031429.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr20:62320907 G>T maps to ENST00000482936 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr15:41769658 C>T maps to NM_015138.4 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74653437 G>A maps to NM_001015055.1 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:60194300 C>T maps to NM_021136.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr11:63488085 A>G maps to ENST00000377819 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:1840947 G>A maps to NM_178568.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr17:1840686 G>A maps to NM_178568.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:179025749 C>T maps to NM_025158.3 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr10:70105525 C>A maps to NM_017987.4 *642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr2:218940429 G>A maps to NM_198483.3 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr16:12136838 C>T maps to NM_032167.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr17:42390844 G>A maps to NM_001144825.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr7:87369181 T>C maps to NM_138290.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr8:93017507 C>G maps to NM_175634.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:93026863 G>A maps to NM_175634.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr8:92988172 A>T maps to NM_175634.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NK-01A-12D-A34U-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NK-01A-12D-A34U-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr1:25233873 C>T maps to NM_001031680.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr1:25254067 G>T maps to NM_001031680.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35546638 A>C maps to NM_001135999.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr9:35548056 G>A maps to NM_001135999.1 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr19:49517860 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:49507652 G>A maps to NM_006666.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr5:33937287 G>A maps to NM_016568.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:137321059 C>T maps to NM_002957.4 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr6:33168112 C>T maps to ENST00000374685 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:165370514 C>T maps to NM_006917.4 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr1:165414094 G>T maps to NM_006917.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:72428399 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:39075635 C>T maps to NM_000540.2 D4900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr19:38959778 C>T maps to NM_000540.2 D1185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr19:38934380 C>T maps to NM_000540.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr19:38964030 C>T maps to NM_000540.2 D1260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr1:237947731 G>A maps to NM_001035.2 T4240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr1:237972269 C>T maps to NM_001035.2 R4790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr1:237801683 C>T maps to NM_001035.2 L2274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr1:237754088 T>A maps to NM_001035.2 A1319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr1:237893571 C>T maps to NM_001035.2 V3617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:237711847 G>A maps to NM_001035.2 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:237870321 C>T maps to NM_001035.2 I3218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr1:237666714 G>A maps to NM_001035.2 K841K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr1:237774129 G>A maps to NM_001035.2 P1584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr1:237982394 C>T maps to NM_001035.2 I4831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:237756846 T>C maps to NM_001035.2 D1449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr1:237923149 T>C maps to NM_001035.2 C3800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr1:237619980 C>T maps to NM_001035.2 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr1:237617789 C>T maps to NM_001035.2 H464H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr1:237947647 C>T maps to NM_001035.2 N4212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:33990172 C>T maps to NM_001036.3 N2075N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:33835895 C>T maps to NM_001036.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr15:33954938 C>T maps to NM_001036.3 G1736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46I-01A-12D-A26M-08 chr15:33941373 C>T maps to NM_001036.3 D1360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr15:33938649 C>T maps to NM_001036.3 C1288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr15:33988495 C>T maps to NM_001036.3 R1980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr15:33795932 C>T maps to NM_001036.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:34150102 C>T maps to NM_001036.3 D4710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr15:34102838 C>T maps to NM_001036.3 R3396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr15:34015066 C>T maps to NM_001036.3 D2257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr15:34157423 A>C maps to NM_001036.3 G4870G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:33927870 C>T maps to NM_001036.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:34014940 C>T maps to NM_001036.3 S2215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:34078151 C>T maps to NM_001036.3 I3186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:34130096 C>T maps to NM_001036.3 D3972D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr15:34093024 G>C maps to NM_001036.3 V3295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:153580144 C>T maps to NM_080388.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr1:153520901 T>G maps to NM_002960.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:153516336 G>A maps to NM_002961.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:153409548 G>A maps to NM_001045479.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr1:153330776 G>A maps to NM_002965.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:6695685 C>T maps to NM_005980.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:10335296 A>T maps to NM_004230.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10625417 G>A maps to NM_001166215.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr11:18267019 C>T maps to NM_030754.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:45761022 A>G maps to NM_014016.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:45746681 C>T maps to NM_014016.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr13:23912524 C>T maps to NM_014363.4 L1830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr19:5598869 G>A maps to NM_014649.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:234237187 C>T maps to NM_000541.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr2:234237162 C>T maps to NM_000541.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr23:134990667 A>C did not map to a codon.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr23:134988580 A>C did not map to a codon.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr23:134988206 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HL-01A-11D-A364-08 chr16:51175652 G>A maps to ENST00000251020 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:76755233 C>T maps to NM_171999.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:76756937 C>T maps to NM_171999.2 G1173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:76753097 C>T maps to NM_171999.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:76754984 C>T maps to NM_171999.2 S998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:50408259 G>A maps to NM_020436.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HK-01A-11D-A364-08 chr20:50407254 G>A maps to NM_020436.3 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr19:14199509 C>T maps to ENST00000269724 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr17:48193047 C>T maps to NM_174920.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr6:130467206 A>G maps to ENST00000457563 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:169656273 C>T maps to NM_182610.2 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr7:92734006 T>C maps to NM_017654.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr7:92735119 T>C maps to NM_017654.3 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46E-01A-31D-A257-08 chr7:92764068 G>A maps to NM_152703.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr7:92763219 G>A maps to NM_152703.2 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr7:92761816 C>T maps to NM_152703.2 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:35539723 A>T maps to NM_015474.3 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr22:44371975 C>T maps to NM_015380.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:44373825 C>T maps to NM_015380.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:44377305 A>G maps to NM_015380.4 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr17:73663473 C>T maps to NM_013260.6 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:73695893 G>A maps to NM_013260.6 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:153830730 C>T maps to NM_024632.5 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr22:50862021 C>T maps to ENST00000216061 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50832366 G>A maps to ENST00000216061 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr9:136594987 C>T did not map to a codon.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr9:136595288 C>T maps to NM_007101.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr9:136597690 C>A maps to NM_007101.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr9:136573528 C>T maps to NM_007101.3 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:26722946 C>T maps to ENST00000379061 C647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr6:148865534 C>T maps to NM_015278.3 Q977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr6:148854056 C>T maps to NM_015278.3 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L2-01A-31D-A41K-08 chr6:148865284 A>T maps to NM_015278.3 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr23:128927060 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr23:128927069 C>A did not map to a codon.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr2:200233397 A>T maps to NM_001172509.1 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:66458254 G>T maps to NM_016038.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr22:50893709 G>A maps to ENST00000337034 A1509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50901732 A>G maps to ENST00000337034 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr11:9838384 A>G did not map to a codon.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:123834910 A>G maps to NM_001167856.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:123830008 G>A maps to NM_001167856.1 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr19:1113560 C>T maps to NM_014963.2 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr19:36018433 C>T maps to NM_001166034.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr19:36018835 G>A maps to NM_001166034.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:36017620 G>A maps to NM_001166034.1 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:50154650 G>A maps to NM_021228.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:75146409 C>T maps to NM_005697.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr6:28554184 G>A maps to NM_052923.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:47455418 G>A maps to NM_012235.2 N1255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:47455370 C>T maps to NM_012235.2 V1271V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5748-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:1543258 G>T maps to NM_003693.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:102116397 C>T maps to NM_005063.4 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:31188566 C>T maps to ENST00000311943 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:224463598 G>T maps to NM_003469.4 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr2:224462647 C>T maps to NM_003469.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr15:51975310 A>G maps to NM_013243.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:62038407 G>C maps to NM_002411.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr23:18275110 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr3:38835294 C>T maps to NM_006514.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr3:38766806 T>C did not map to a codon.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr3:38743402 G>A maps to NM_006514.2 F1528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr3:38924807 C>A maps to ENST00000302328 L1045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr2:166908357 G>A maps to NM_001165963.1 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr2:166848110 G>A maps to NM_001165963.1 R1892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35524560 C>T maps to NM_199037.3 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35530126 C>T maps to NM_001037.4 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr2:166165900 G>A maps to NM_001040142.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:166231266 C>T maps to NM_001040142.1 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:166245292 G>A maps to NM_001040142.1 A1659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:118039352 G>A maps to NM_004588.4 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:166020179 C>T maps to NM_006922.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:165947856 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:165984284 G>A maps to NM_006922.3 Y1083Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr11:123516293 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr17:62022974 G>A maps to NM_000334.4 G1155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:62019305 G>A maps to NM_000334.4 L1446L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-YL-A8HL-01A-11D-A364-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:38618224 G>A maps to NM_001099404.1 N1146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr3:38627373 G>A maps to NM_001099404.1 Y865Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:38592950 G>T maps to NM_001099404.1 R1638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr3:38592255 G>A maps to NM_001099404.1 D1869D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167262809 A>T maps to NM_002976.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr2:167279861 G>T maps to NM_002976.2 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr2:167289253 G>T maps to NM_002976.2 Y722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr12:52200654 C>T maps to NM_014191.2 F1795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr2:167089855 T>A maps to ENST00000303354 G1307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr2:167133600 G>A maps to ENST00000303354 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr1:151139434 C>T maps to NM_024041.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr12:6471350 C>T maps to NM_001159576.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:23364120 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:53444039 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144895095 G>A maps to NM_182706.3 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:175265861 T>C maps to NM_024583.4 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:43687178 G>A maps to NM_173050.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:43716063 G>A maps to NM_173050.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr11:9072167 G>A maps to ENST00000457346 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:9049016 C>T maps to ENST00000457346 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:65303494 G>A maps to NM_020680.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr11:65302784 G>T maps to NM_020680.3 E440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:100732506 G>T maps to NM_017988.4 G783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:43956029 G>A maps to NM_002999.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:43961679 C>A maps to NM_002999.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:233680 C>T maps to NM_004168.2 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:161326631 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:3990603 G>A maps to NM_152744.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr7:3681626 A>T maps to NM_152744.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr7:4088995 G>A maps to NM_152744.3 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr7:4119140 T>G maps to NM_152744.3 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:4198176 C>T maps to NM_152744.3 Q1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:4285376 C>T maps to NM_152744.3 G2107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:71431640 G>A maps to NM_001144952.1 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:192711276 C>T maps to NM_004657.5 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:113830892 G>A maps to NM_006843.2 H280H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:113875850 G>A maps to NM_138432.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr17:75205503 C>G maps to NM_001039573.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:75199712 G>A maps to NM_001039573.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:5038193 G>A maps to NM_014692.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:139350602 G>A maps to NM_014866.1 R1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:139370680 C>A maps to NM_014866.1 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:177902749 G>T maps to NM_033127.2 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:39536388 C>T maps to NM_006364.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr20:18505661 C>T maps to NM_001172745.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr20:18496337 C>T maps to NM_001172745.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:110394175 C>A maps to NM_006323.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr10:75519788 G>A maps to NM_198597.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr10:12200104 G>A did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr17:80282490 T>A maps to NM_003004.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:25823677 G>A maps to NM_015187.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:151340693 G>A maps to ENST00000435071 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:169677594 G>A maps to NM_000655.4 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50649338 C>T maps to NM_031454.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:84694821 A>G maps to NM_152754.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:84644454 G>A maps to NM_152754.2 C541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:84694863 C>T maps to NM_152754.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:84751068 G>A maps to NM_152754.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:82997120 C>T maps to NM_012431.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr3:50214256 G>A maps to NM_004186.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:90763059 G>A maps to NM_198925.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MG-01A-11D-A364-08 chr9:91994251 G>A maps to NM_006378.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:102737390 G>A maps to NM_017893.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:102739700 G>A maps to NM_017893.2 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:102740673 A>G maps to NM_017893.2 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KQ-01A-12D-A364-08 chr5:9122874 G>A maps to NM_003966.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:115815885 C>T maps to ENST00000257414 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr19:4543618 C>T maps to NM_032108.3 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:151109505 G>A maps to NM_001178061.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:151105901 G>A maps to NM_001178061.1 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:48054505 A>G maps to NM_153618.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z7-01A-11D-A41K-08 chr15:74703249 G>A maps to NM_003612.3 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr15:74703249 G>A maps to NM_003612.3 H572H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:48477396 G>A maps to ENST00000004980 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr6:76373049 A>G maps to NM_015571.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr3:101047391 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:87369092 G>A maps to NM_004261.3 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr10:13375854 T>C maps to NM_012247.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:26135153 G>A maps to NM_020451.2 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr4:77941725 C>T maps to ENST00000510515 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:4828124 C>T maps to NM_144605.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr2:242276829 A>G maps to ENST00000391972 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr2:242289492 C>T maps to ENST00000391972 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr22:42377715 G>A maps to NM_145733.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:56598641 G>A maps to NM_004574.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr23:118783980 G>A did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr16:1990837 G>T maps to ENST00000399753 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:31906940 G>A maps to NM_178865.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:43135506 G>A maps to NM_006811.2 C248C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:94756666 T>C maps to NM_001100607.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:95034588 C>T maps to NM_006215.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr14:94776284 G>A maps to NM_001756.3 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:94935862 T>C maps to NM_175739.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:61390554 G>A maps to NM_080475.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr18:61570298 A>T maps to NM_001143818.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:61305231 C>T maps to NM_002974.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:173876635 G>A maps to NM_000488.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr7:100780351 G>A maps to NM_000602.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775169 T>C maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775171 G>A maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr7:100779050 C>T maps to NM_000602.3 N352N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100779041 C>T maps to NM_000602.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr2:224849662 C>T maps to NM_001136530.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:224866368 G>A maps to NM_001136530.1 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:1679917 C>T maps to NM_002615.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:1673174 G>A maps to NM_002615.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr11:57367488 C>A maps to ENST00000403558 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:75277585 G>T maps to NM_001235.2 V64V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-A4ZV-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:167508390 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:210415060 C>T maps to NM_019605.3 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:42281463 C>T maps to NM_015559.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:42643647 C>T maps to NM_015559.2 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr3:47103827 G>A maps to NM_014159.6 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr3:47161879 C>A maps to NM_014159.6 E1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:9482198 G>A maps to ENST00000407969 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:9515128 C>A maps to ENST00000407969 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:140439118 G>T maps to NM_030648.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:150936117 C>T maps to NM_001145415.1 S1190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:135176062 G>A maps to ENST00000372169 H1834H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:135204623 G>T maps to ENST00000372169 I787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:27285094 C>T maps to NM_178860.4 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr22:26701984 C>T maps to NM_021115.4 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:26688422 C>A maps to NM_021115.4 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr22:26761443 C>T maps to NM_021115.4 Y902Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:29884627 G>A maps to NM_201575.2 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr22:30736750 T>C maps to NM_005877.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WX-01A-21D-A41K-08 chr1:38444714 G>A maps to NM_006802.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr2:198267738 C>T maps to NM_012433.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:65826470 C>T maps to NM_006842.2 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr16:70589036 G>A maps to NM_012426.4 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:149898266 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:32009507 C>T maps to NM_001007467.1 Q912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52960106 G>A maps to NM_016329.3 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:7239527 G>A maps to NM_001018039.1 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr4:154709576 G>A maps to NM_003013.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr19:19120891 G>A maps to NM_001017392.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr19:19115403 C>T maps to NM_001017392.3 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19136508 T>C maps to NM_001017392.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr21:33044275 C>T maps to NM_020706.2 Q960Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr23:1712959 G>A did not map to a codon.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr23:1712836 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:1714290 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:99849498 C>T maps to NM_032870.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74732289 T>A maps to NM_003016.4 K207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:74732290 C>A maps to NM_003016.4 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr11:94800908 C>A maps to NM_032102.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr12:46316919 A>C maps to NM_004719.2 S1308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:29475268 G>A maps to NM_005626.4 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:132250709 C>T maps to NM_004592.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:85890790 G>A maps to NM_198843.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr5:156184678 C>T maps to NM_000337.5 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:67206952 A>T did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:67147852 G>A maps to ENST00000237247 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:134491489 G>A maps to NM_001143676.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr8:8238939 G>C maps to NM_001080826.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:77450875 C>T maps to NM_024776.2 P1100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:67759501 A>G maps to NM_013257.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr3:20215803 T>G maps to NM_001012410.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr3:20215977 G>A maps to NM_001012410.3 R349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:20216080 G>A maps to NM_001012410.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr10:72576637 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:25294510 C>T maps to NM_001039948.2 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:25315922 C>T maps to NM_001039948.2 N1107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:2280071 C>T maps to NM_014853.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr22:40803532 C>T maps to NM_015705.4 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2762502 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2762617 C>T maps to NM_003021.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2767625 C>T maps to NM_003021.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:101960817 C>T maps to ENST00000306803 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:6760818 C>T maps to NM_005490.2 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:6760866 C>T maps to NM_005490.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr9:130506866 C>T maps to NM_170600.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr9:130507028 C>T maps to NM_170600.2 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr9:130511761 G>A maps to NM_170600.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr8:19218825 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:38041480 C>T maps to NM_018957.3 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:235951389 T>C maps to NM_014521.2 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:15311357 C>T maps to NM_004844.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:15311377 G>A maps to NM_004844.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:249118996 G>T maps to NM_030645.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr4:152048835 C>T maps to NM_001009555.3 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr9:17791306 C>T maps to NM_003026.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr10:105361686 C>A maps to ENST00000369774 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:105362574 C>T maps to ENST00000369774 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:171821587 T>G maps to NM_001017995.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr4:170037773 C>T maps to NM_020870.3 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr5:145442110 G>A maps to NM_152550.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:8235131 G>A maps to NM_018986.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr4:8228812 G>A maps to NM_018986.3 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:8230216 G>C maps to NM_018986.3 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:51217186 C>T maps to ENST00000391814 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr19:51217084 G>A maps to ENST00000391814 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr19:51172429 C>A maps to ENST00000391814 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr19:51219609 G>A maps to ENST00000391814 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr11:70336435 T>G maps to ENST00000338508 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:70332443 G>A maps to ENST00000338508 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:70338439 G>A maps to ENST00000338508 N807N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr8:145154288 G>A maps to NM_030974.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7535019 C>A maps to NM_001040.3 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7536651 C>T maps to NM_001040.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr1:154938796 A>G maps to NM_001130040.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr9:91657076 C>T maps to NM_016848.5 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:46638333 A>G maps to NM_024745.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:4288302 C>T maps to NM_020209.3 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr19:4282874 C>T maps to NM_020209.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:154459159 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr13:26620947 C>T maps to NM_001007538.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:42403326 G>A maps to NM_001080505.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr19:41096645 G>T maps to NM_138392.3 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:601571 G>A did not map to a codon.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:591825 A>T did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr3:157820523 G>A maps to NM_003030.4 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr6:146264542 G>A maps to ENST00000367503 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:146266672 G>A maps to ENST00000367503 Y474Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr5:132158688 C>T maps to NM_001172700.1 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr5:132160410 A>G maps to NM_001172700.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr23:9912814 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:9841701 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:9912931 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr23:9900640 G>T did not map to a codon.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr4:77677869 C>T maps to NM_020859.3 Q1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr23:50378348 G>A did not map to a codon.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr23:50376382 A>G did not map to a codon.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr23:50377642 G>T did not map to a codon.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr3:164739051 G>A maps to NM_001041.3 G1073G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr3:164739069 G>T maps to NM_001041.3 I1067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr11:117060950 G>A maps to NM_001040455.1 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:117066582 C>T maps to NM_001040455.1 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:117062992 G>A maps to NM_001040455.1 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr11:117052520 A>G did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr11:407862 G>A maps to NM_021805.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:406439 G>A maps to NM_021805.2 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr20:3673296 G>A maps to NM_023068.3 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr19:51918363 T>G did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr19:50462137 G>A maps to NM_052884.2 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:50461936 C>A maps to NM_052884.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:52002815 G>T maps to NM_053003.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:52130799 G>A maps to ENST00000222107 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr19:52115642 G>A maps to ENST00000222107 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr19:51955818 C>T maps to NM_014442.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr19:51629377 C>T maps to NM_014441.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:51628470 T>G maps to NM_014441.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:111592579 C>T maps to NM_015191.1 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr11:116827690 G>A maps to ENST00000445177 C114C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:116718255 C>T maps to ENST00000445177 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr6:100841375 G>T maps to ENST00000262901 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr21:38114058 C>T maps to NM_005069.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:38072204 C>T maps to NM_005069.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr14:39597481 A>T did not map to a codon.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr11:65414868 C>T maps to NM_153253.29 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65409030 C>T maps to NM_153253.29 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:65412535 C>A maps to NM_153253.29 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:72152318 C>A maps to NM_015556.1 I1115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr1:232600813 G>A maps to NM_020808.3 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr1:232650662 G>A maps to NM_020808.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:232649717 G>A maps to NM_020808.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr19:38655513 G>A maps to NM_015073.1 A1392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr19:38633279 C>A maps to NM_015073.1 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:38610374 G>A maps to NM_015073.1 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr20:1600529 G>A maps to NM_006065.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr20:1559026 G>A maps to NM_006065.3 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr20:1592129 G>A maps to NM_001135844.1 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr20:1459193 C>A maps to NM_001122962.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr6:13592061 C>A maps to NM_012241.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:4174910 G>A maps to NM_016539.2 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:79873381 G>A maps to NM_016538.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:45233548 C>T maps to NM_016932.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:45236003 C>T maps to NM_016932.4 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:60976280 C>T maps to ENST00000381716 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FP-01A-21D-A364-08 chr3:170078821 C>A maps to NM_005414.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:54635835 A>G did not map to a codon.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr20:35261965 G>A maps to NM_032214.2 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:48422197 C>T maps to NM_020846.1 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr13:103701636 A>G did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr23:153716035 C>T did not map to a codon.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr2:219249917 C>A maps to NM_000578.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr2:219259417 G>T maps to NM_000578.3 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67980407 G>A maps to NM_005072.4 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr20:44670162 C>A maps to NM_001134771.1 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr20:44682326 G>A maps to NM_001134771.1 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr15:34528967 C>A maps to NM_133647.1 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr15:34527451 C>T maps to NM_133647.1 K1097K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:1083908 G>A maps to NM_006598.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr3:124802838 G>A maps to NM_001195483.1 D680D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:124906082 G>A maps to NM_001195483.1 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:122755607 C>T maps to NM_022444.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr17:26818587 G>A maps to NM_001145975.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:45188747 G>A maps to NM_022829.5 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:135392944 G>A maps to NM_012450.2 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:6606329 G>A maps to NM_177550.3 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:6610466 C>T maps to NM_177550.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:43248312 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:43221186 C>A maps to NM_007163.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr13:99354750 T>C maps to NM_005073.3 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr13:99362007 G>A maps to NM_005073.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr6:111498552 C>T maps to NM_018593.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:6945090 C>T maps to NM_153357.1 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr23:73740920 C>T did not map to a codon.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr23:73745590 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:66267451 T>C maps to NM_004694.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr17:66267673 C>T maps to NM_004694.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:66267676 T>G maps to NM_004694.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:60098740 T>C maps to NM_004731.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:61412649 G>A maps to NM_194298.2 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr11:22382483 G>A maps to NM_020346.2 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr12:100811861 G>T maps to NM_139319.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:61596499 G>C maps to NM_022082.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:119013557 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:228563578 C>T maps to NM_025243.3 W284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr2:228564079 G>A maps to NM_025243.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr19:15072860 G>A maps to NM_005071.1 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:63065163 G>A maps to NM_001039752.3 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:64368359 C>T maps to NM_144585.2 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:110752469 C>T maps to NM_033125.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr14:23821249 C>T maps to NM_020372.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr6:160679378 G>A maps to NM_003058.3 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:3287258 C>A maps to ENST00000436008 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr5:131722815 G>T maps to ENST00000435065 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr6:43267186 C>T maps to ENST00000372585 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr11:62767262 G>A maps to ENST00000430500 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr11:63176238 C>T maps to NM_080866.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr5:138714918 G>T maps to NM_152685.3 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr2:220028151 G>A maps to NM_001144890.1 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr14:92958550 C>T maps to NM_153646.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr15:48431346 C>A maps to NM_205850.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:113748107 G>T maps to NM_024959.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79682083 C>T maps to ENST00000331531 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:4841188 G>A maps to NM_003562.4 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr2:172666118 G>A maps to NM_003705.3 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr7:95750980 A>G maps to NM_001160210.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:70276514 C>T maps to NM_152707.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr22:41169987 T>C maps to NM_006358.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:18072395 C>T maps to NM_031481.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:130854175 A>G maps to ENST00000373066 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr3:66428191 G>A maps to NM_173471.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr6:46623670 C>A maps to NM_004277.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr10:101373522 G>A maps to NM_031212.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:128688339 C>T maps to NM_031291.2 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:8195890 G>A maps to NM_201520.1 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:23423700 C>T maps to NM_016612.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr7:87476438 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:156180189 C>T maps to NM_014655.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr5:110097208 C>T maps to NM_138773.1 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr5:110097083 C>T maps to NM_138773.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:1508387 C>A did not map to a codon.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr23:1508389 C>G did not map to a codon.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr17:78222019 C>T maps to NM_173626.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:78197132 C>T maps to NM_173626.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr5:149360520 T>A maps to NM_000112.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:107423292 G>A maps to NM_000111.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr7:103017288 G>A maps to ENST00000354356 D671D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:35923138 C>T maps to NM_052961.3 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:35980126 G>A maps to NM_052961.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:35987304 G>A maps to NM_052961.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:205897956 G>A maps to NM_134325.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:205899136 G>A maps to NM_134325.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr19:17608155 G>A maps to NM_198580.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr9:131107631 C>G maps to NM_005094.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr15:85461835 G>T did not map to a codon.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr15:45555256 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:86900403 C>T maps to NM_022127.2 W501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:73103988 C>T maps to NM_018344.5 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr12:8083193 C>T maps to NM_006931.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr12:8086489 T>A maps to NM_006931.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr1:9099649 G>A maps to NM_003039.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:130167747 C>A maps to NM_014580.3 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:9828094 T>G maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr1:26371584 A>G maps to NM_001004434.1 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27481119 C>T maps to NM_003459.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr8:118169990 C>T maps to NM_173851.2 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr8:118169933 C>T maps to NM_173851.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr8:118175680 C>T maps to NM_173851.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:42072552 G>A maps to NM_006345.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr4:25678364 C>T maps to NM_006424.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:25667861 G>A maps to NM_006424.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:25665887 C>T maps to NM_006424.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:67507942 C>T maps to NM_015139.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:137245293 C>T maps to NM_001008783.1 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:16677422 G>A maps to NM_024881.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr6:118598701 G>A maps to NM_001029858.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:234367479 C>T maps to NM_173508.2 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:58060840 A>G maps to NM_001080455.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150847344 G>A maps to NM_078483.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150718706 T>C did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr21:43967226 A>C maps to NM_018964.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:79226448 G>A maps to NM_001037984.1 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:165809220 A>G maps to ENST00000409662 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:165765266 C>A maps to ENST00000409662 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:165755096 G>A maps to ENST00000409662 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:46757762 C>G maps to NM_018976.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr3:50255181 C>T maps to NM_006841.4 H255H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr14:61503801 C>T maps to NM_001172702.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr5:54993714 A>T maps to NM_173514.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr2:196581640 C>T maps to NM_001127257.1 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr2:196545260 A>G maps to NM_001127257.1 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:18254428 G>A maps to NM_001145195.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:22275305 G>A maps to NM_001135153.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr12:56628744 T>A maps to NM_001135195.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:33171400 C>T maps to NM_006979.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:103188796 G>A maps to NM_001135146.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:44503054 C>A maps to NM_000341.3 Y127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:44541026 T>C maps to NM_000341.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr1:205768181 G>T maps to NM_173854.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr11:57182086 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:31838426 C>T maps to NM_025257.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr1:75805313 A>G maps to NM_152697.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:75708579 C>T maps to NM_152697.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr1:8390956 C>T maps to ENST00000377479 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr1:8390701 C>T maps to ENST00000377479 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:8386058 C>T maps to ENST00000377479 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr5:33947261 G>A maps to NM_001012509.2 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr8:142226016 G>A maps to NM_001080431.1 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:142222364 G>A maps to NM_001080431.1 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:142231718 G>A maps to NM_001080431.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:29292060 C>T maps to NM_001135919.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr17:19451299 G>A maps to ENST00000395585 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S0-01A-11D-A41K-08 chr17:19584866 G>T maps to NM_152908.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:42340028 G>A maps to NM_000342.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:42333172 G>A maps to NM_000342.3 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr17:42333043 G>T maps to NM_000342.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:42335880 C>T maps to NM_000342.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr2:162804173 T>C maps to NM_001178015.1 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr20:3214873 G>A maps to NM_001174090.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr2:27907926 A>G maps to NM_018158.2 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr7:150773113 T>C maps to NM_003040.3 R1162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr7:150761317 G>A maps to NM_003040.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr2:220504356 G>A maps to NM_201574.2 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74492357 G>A maps to NM_021196.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr5:139744178 C>T maps to ENST00000507527 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr5:139743378 C>T maps to ENST00000507527 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr5:139745495 C>T maps to ENST00000507527 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:32500780 T>C maps to NM_000343.3 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:18916804 G>A maps to NM_152351.3 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr17:18923108 C>T maps to NM_152351.3 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18855616 C>T maps to NM_152351.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18918410 G>A maps to NM_152351.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:26743039 G>T maps to NM_178498.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr11:26725365 T>C maps to NM_178498.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:31499067 G>A maps to ENST00000431354 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr16:31498983 C>G maps to ENST00000431354 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:31500021 G>A maps to ENST00000431354 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr19:17999205 C>T maps to NM_000453.2 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJ3-01A-11D-A41K-08 chr3:10967723 G>A maps to NM_014229.1 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:304490 G>A maps to NM_003044.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:347147 G>A maps to NM_016615.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr23:115576108 G>A did not map to a codon.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:49797194 G>A maps to NM_014037.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:110716608 G>T maps to NM_001010898.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:1244330 C>T maps to NM_182632.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:1213642 G>A maps to NM_001003841.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:55735847 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:28530243 G>A maps to ENST00000394821 C630C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:44463273 C>T maps to NM_201649.2 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:139106349 G>A maps to ENST00000280612 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:17400869 C>T maps to NM_001164771.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr8:17418004 G>A maps to NM_001164771.1 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:47951337 G>A maps to NM_015063.2 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr14:70633726 G>A maps to NM_183002.1 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr1:173495814 A>G maps to NM_178527.3 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr5:482773 G>A maps to NM_004174.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67305046 C>T maps to NM_004594.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:135067781 G>T did not map to a codon.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr20:48479504 C>G maps to ENST00000417961 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr12:21392116 T>C maps to NM_006446.4 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:21030808 C>T maps to NM_019844.2 Y358Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr11:74904263 C>A maps to NM_007256.4 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:92459272 C>T maps to NM_013272.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr20:61288285 C>T maps to NM_016354.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:61288117 C>T maps to NM_016354.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr5:101585437 C>T maps to NM_180991.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:70744218 C>T maps to NM_030958.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:70585421 G>A maps to NM_030958.2 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:101813485 G>A maps to NM_173488.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr5:101795411 G>A maps to NM_173488.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:101834536 G>A maps to NM_173488.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr17:33690214 G>T maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:33769198 G>A maps to NM_144682.5 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr17:33592769 C>T maps to NM_144975.3 R847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr10:98764484 G>A maps to NM_003061.2 Y1225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr10:98806791 C>T maps to NM_003061.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:98761033 C>T maps to NM_003061.2 T1480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr4:20255578 C>A maps to ENST00000273739 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:20597355 C>T maps to ENST00000273739 C1086C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr5:168093524 C>T maps to NM_003062.2 T1502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr5:168112856 G>A maps to NM_003062.2 N1130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:168114117 G>A maps to NM_003062.2 C1060C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr13:84454930 G>A maps to NM_052910.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr23:144906345 C>T did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr23:144906445 G>T did not map to a codon.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr23:144904389 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:144904205 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr23:144904182 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr3:164907133 G>A maps to NM_014926.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:164906503 G>A maps to NM_014926.2 C705C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:142716668 G>A did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr23:142718313 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr13:88328680 T>C maps to NM_015567.1 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:59179239 G>A maps to NM_024755.2 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:59191687 C>T maps to NM_024755.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr18:46447810 G>A maps to NM_005904.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr13:37453544 G>A maps to NM_001127217.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr23:128599697 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr23:128599548 C>G did not map to a codon.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr23:128599495 C>T did not map to a codon.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr23:128599588 C>G did not map to a codon.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr23:128624099 C>T did not map to a codon.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:217297569 C>T maps to NM_014140.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:56575859 G>A maps to NM_003075.3 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:50483695 C>T maps to NM_003076.4 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:53436012 G>C did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:45740516 G>A maps to NM_148674.3 R1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:152857071 C>T maps to NM_030663.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr22:39908031 G>C did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr17:18219933 G>A maps to NM_144775.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:18866182 T>C maps to ENST00000389467 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:2076131 C>T maps to NM_017575.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:183514378 C>T maps to ENST00000367537 Q765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr14:70477513 A>G maps to NM_001034852.1 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr14:70480115 G>A maps to NM_001034852.1 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr14:70490003 C>T maps to NM_001034852.1 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr14:70420249 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:130930031 G>T maps to NM_017951.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr6:123127402 G>A maps to NM_006714.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:28285051 C>T maps to NM_014474.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:28285225 T>C maps to NM_014474.2 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr9:33056917 C>T maps to NM_018225.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr9:33057682 A>G maps to NM_018225.2 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:98634698 C>T maps to NM_020429.2 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:62582226 T>C maps to NM_022739.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr22:21213457 C>T maps to NM_004782.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MU-01A-11D-A377-08 chr1:227935844 G>A maps to NM_053052.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr6:84290294 A>G maps to NM_014841.2 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr14:62233592 G>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:139289315 G>A maps to NM_003086.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:121776373 G>A maps to ENST00000379533 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr10:88718534 G>A maps to NM_003087.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr20:1281298 G>T maps to ENST00000381876 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:96963421 G>A maps to NM_014014.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:70130360 C>T maps to NM_006857.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:31734424 G>A maps to ENST00000446633 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:31744301 G>A maps to ENST00000446633 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr15:25221556 C>A maps to NM_022805.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31998064 G>A maps to NM_003098.2 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:121554094 T>A maps to NM_021021.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr2:1271264 C>T maps to NM_018968.3 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr3:63638398 T>C maps to NM_001080537.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr23:70280883 C>A did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:17885262 G>A maps to ENST00000417048 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr7:17838695 G>A maps to ENST00000417048 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:17861182 G>T maps to ENST00000417048 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr8:82727589 C>A maps to NM_152836.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr11:130781572 G>A maps to NM_014758.2 Q590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr5:122161781 G>A maps to NM_003100.2 W417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:122272466 T>C maps to ENST00000395451 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:186188121 G>A did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:101589257 G>A maps to NM_152628.3 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr8:101612648 T>C maps to NM_152628.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr8:101612610 A>T maps to NM_152628.3 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:101586125 G>A maps to NM_152628.3 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:101661555 G>A maps to NM_152628.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr11:65620243 C>A maps to NM_152760.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:75941790 C>T maps to NM_153271.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr3:125176112 A>G maps to NM_003794.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FO-01A-21D-A364-08 chr1:179310183 C>A maps to NM_003101.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr12:53509272 G>A maps to NM_003578.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr12:53509946 C>T maps to NM_003578.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr12:53512167 C>T maps to NM_003578.3 Y271Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:53514640 C>T maps to NM_003578.3 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:138586194 C>T maps to NM_001012415.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:602480 C>T maps to NM_005632.2 C896C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:34924072 T>C maps to NM_138927.1 L846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:34924854 G>A maps to NM_138927.1 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB20-01A-12D-A41K-08 chr4:186545478 G>A maps to ENST00000355634 N464N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:186536197 C>T did not map to a codon.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:22415643 C>T maps to NM_005775.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr8:22426716 G>A maps to NM_005775.4 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr10:108427559 G>A maps to NM_001013031.1 C730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr10:108434805 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:108389095 C>T maps to NM_001013031.1 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr4:7741957 C>T maps to NM_020777.2 N1149N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr10:106976776 C>T maps to NM_014978.1 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr10:106937889 C>T maps to NM_014978.1 D656D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIR-01A-11D-A41K-08 chr10:107022172 C>T maps to NM_014978.1 N1176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:106976776 C>T maps to NM_014978.1 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:121454218 C>T maps to NM_003105.5 C1211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:121458729 G>A maps to NM_003105.5 E1272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:121475004 G>A maps to NM_003105.5 S1541S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:39237758 G>A maps to NM_005633.3 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:39250101 A>G maps to NM_005633.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L2-01A-31D-A41K-08 chr2:39262595 G>A maps to NM_005633.3 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr13:112722310 G>A maps to NM_005986.2 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:137483985 C>T maps to NM_004189.2 S120S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:139587163 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr5:157078492 G>A maps to NM_178424.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr11:16071442 G>T maps to NM_001145819.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:16010576 G>A maps to NM_001145819.1 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr11:16117661 C>T maps to NM_001145819.1 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr11:16007826 G>A maps to NM_001145819.1 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr12:53777377 C>G maps to NM_138473.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr12:53776770 C>A maps to NM_138473.2 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr2:231155226 A>G maps to NM_007237.4 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SC-01A-11D-A377-08 chr17:46002396 G>A maps to NM_003110.5 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr17:45993544 C>G maps to NM_003110.5 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr2:174777795 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:21469340 T>C maps to NM_003112.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr2:215274873 A>G maps to NM_024532.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:118635825 G>A maps to NM_206996.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:26910635 G>A maps to NM_006461.3 Q860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:26904748 C>A maps to NM_006461.3 E1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:26912638 G>A maps to NM_006461.3 H591H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr10:22634709 G>A maps to ENST00000376603 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:123594142 G>A maps to NM_001174046.1 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:123595094 T>C maps to NM_001174046.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr23:140785742 T>A did not map to a codon.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr23:140785701 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:144337273 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr23:144337211 G>T did not map to a codon.
Sequencing variant TCGA-J9-A8CK-01A-11D-A34U-08 chr23:144337276 T>C did not map to a codon.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr23:52825633 G>A did not map to a codon.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr2:32312618 A>G maps to NM_014946.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:57108292 T>A maps to NM_181727.1 *191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:24860351 C>T maps to ENST00000424834 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr13:24864977 G>A maps to ENST00000424834 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:133712383 G>A maps to NM_174927.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr20:48525009 T>G maps to NM_006038.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr17:48626525 G>C maps to NM_022827.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BR-01A-32D-A257-08 chr1:16727314 C>A maps to NM_198546.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:123850196 G>A maps to NM_145207.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:45695157 G>A maps to NM_024063.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:45706806 T>C maps to NM_024063.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:48865160 T>C maps to NM_019073.2 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr8:145094891 C>T maps to NM_198572.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:201324530 T>C maps to ENST00000409151 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:201305435 C>T maps to ENST00000409151 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr3:52741716 A>G maps to NM_014041.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr7:99909506 C>T maps to NM_001004351.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr7:99913459 A>G maps to NM_001004351.4 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr5:35712920 G>A maps to NM_024867.3 P949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr2:220348802 C>T maps to NM_005876.4 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:220331956 C>T maps to NM_005876.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:220350131 A>G maps to NM_005876.4 L2558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:16257093 C>T maps to NM_015001.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:16257157 C>T maps to NM_015001.2 R1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr1:16260825 G>A maps to NM_015001.2 V2697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:69223000 C>A maps to NM_145658.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr2:228883535 A>G maps to NM_001142644.1 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr2:228881543 C>T maps to NM_001142644.1 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr2:228890232 G>A maps to NM_001142644.1 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr2:228846443 C>A maps to NM_001142644.1 E1698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:47376807 G>C maps to NM_001080547.1 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:101876610 A>G maps to ENST00000299272 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:147553879 C>T maps to NM_001001325.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr18:12463457 G>T maps to NM_001128626.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr16:29675594 C>A maps to NM_003123.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr20:55914069 G>A maps to ENST00000371258 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:136324288 G>A maps to NM_004598.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr4:167656221 G>A maps to NM_016950.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr4:167713336 C>T maps to NM_016950.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:167833894 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr11:13984531 G>C maps to NM_006108.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:1164337 C>T maps to NM_012445.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr2:139318403 T>C maps to NM_001001664.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2352990 G>A maps to NM_152988.2 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:65561754 G>A maps to NM_181784.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:153012803 G>A maps to NM_006945.4 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:153122526 C>T maps to NM_001014291.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr1:152975780 G>A maps to NM_005416.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:155003969 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:155003601 T>C did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:141694232 C>T maps to NM_030964.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:141694196 G>A maps to NM_030964.3 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:158612200 C>T maps to NM_003126.2 K1579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:158585064 G>A maps to NM_003126.2 D2243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:158605701 C>A did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr1:158639552 T>C maps to NM_003126.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr1:158618310 G>T maps to NM_003126.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr1:158606499 C>A maps to NM_003126.2 G1747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr1:158627400 G>A maps to NM_003126.2 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:158618331 G>A maps to NM_003126.2 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:158639537 G>A maps to NM_003126.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:131381260 C>T maps to NM_001130438.2 G1904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr9:131370159 T>G maps to NM_001130438.2 A1392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr14:65239588 G>T maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr14:65246523 C>T maps to ENST00000389723 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:65260130 G>A maps to ENST00000389723 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:54753665 G>A maps to NM_003128.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:54886367 G>A maps to NM_003128.2 T2107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:54876763 C>T maps to NM_003128.2 R1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:66469125 G>A maps to NM_006946.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66458793 G>A maps to NM_006946.2 H1842H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:66475238 G>A maps to NM_006946.2 H467H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr19:41062019 G>A maps to NM_020971.2 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr19:41007897 C>T maps to NM_020971.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr19:41078059 T>C maps to NM_020971.2 A2485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:41025862 C>T maps to NM_020971.2 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr15:42162705 G>A maps to ENST00000320955 R1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr15:42147469 C>T maps to ENST00000320955 A3125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42162697 G>A maps to ENST00000320955 T1836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:18637463 G>A maps to NM_194285.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:45965848 G>T maps to NM_021199.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr15:45968453 A>G maps to NM_021199.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr15:45968417 C>T maps to NM_021199.2 N258N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:45773896 A>G maps to NM_018079.4 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr16:30715428 C>T maps to NM_006662.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr16:30750171 A>G maps to NM_006662.2 R2937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr16:30750172 A>C maps to NM_006662.2 R2938R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr16:30724641 G>A maps to NM_006662.2 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30747621 T>C maps to NM_006662.2 F2277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30748452 G>A maps to NM_006662.2 P2364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:76029804 G>A maps to NM_080744.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:31754465 G>T maps to NM_000348.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr12:64502787 G>A maps to NM_020762.2 V630V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr1:206610381 C>G maps to ENST00000414359 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:87846499 G>A maps to NM_003130.2 Q48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:11119362 G>A maps to NM_003132.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:62178594 G>A maps to NM_080823.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:62172601 G>T maps to NM_080823.2 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:35840372 G>A maps to ENST00000361690 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr23:153046770 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr23:38016272 A>T did not map to a codon.
Sequencing variant TCGA-EJ-A46E-01A-31D-A257-08 chr23:99917331 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr23:99925823 G>A did not map to a codon.
Sequencing variant TCGA-G9-A9S4-01A-11D-A41K-08 chr17:2222192 G>A maps to NM_021947.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr22:26884137 T>C maps to NM_001013694.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr1:24998070 G>A maps to NM_005839.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr12:119583286 G>A maps to NM_194286.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr12:119563254 G>A maps to NM_194286.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:100479772 G>A maps to NM_015908.5 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr20:60737904 C>A maps to NM_198935.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr5:80809506 T>G maps to ENST00000380182 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr19:18543389 G>A maps to NM_032627.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:109182099 G>A maps to NM_018984.3 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr11:67074409 G>T maps to NM_017857.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr7:149492708 G>A maps to NM_198455.2 W2164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:149477548 C>T maps to NM_198455.2 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr7:149497092 G>C did not map to a codon.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr14:38679034 T>A maps to NM_001049.2 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr22:37602984 G>A maps to NM_001051.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr20:23016215 G>A maps to NM_001052.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr20:23016626 C>T maps to NM_001052.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1129347 C>T maps to NM_001053.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr1:85116178 C>T maps to NM_001166417.1 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr23:48207019 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr23:48054233 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7AV-01A-11D-A32B-08 chr23:48054446 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr23:48053625 A>G did not map to a codon.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr23:52681973 C>A did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr11:130079558 T>G maps to NM_021978.3 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:130059741 G>A maps to NM_021978.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:130060403 G>A maps to NM_021978.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr8:53045684 G>A maps to NM_014682.2 C792C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:53073992 G>A maps to NM_014682.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:53079445 C>G maps to NM_014682.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:53084571 G>A maps to NM_014682.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr8:134472108 C>T maps to NM_173344.2 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr8:134488180 G>C maps to NM_173344.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:70422349 G>A maps to NM_006927.3 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr2:86067398 G>A maps to NM_003896.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr2:107459776 C>T maps to NM_001142351.1 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr2:107460367 G>A maps to NM_001142351.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr17:74625600 C>T maps to NM_018414.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74625189 C>T maps to NM_018414.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74570474 C>T maps to NM_006456.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:130653031 G>A maps to NM_013443.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr12:22354691 C>A maps to NM_003034.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:55020208 C>T maps to NM_015879.2 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:44260379 C>T maps to NM_013305.4 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:17363215 C>T maps to NM_001004470.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr3:52529473 C>T maps to NM_015136.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A724-01A-12D-A32B-08 chr3:52551012 C>T maps to NM_015136.2 C1459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52544489 C>T maps to NM_015136.2 T918T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:52557341 C>A maps to NM_015136.2 G2375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr12:104107520 C>T maps to NM_017564.9 Y1504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:104069708 T>C maps to NM_017564.9 C852C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:104121052 C>T maps to NM_017564.9 F1620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:104140468 A>G maps to NM_017564.9 G2077G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:36524553 C>T maps to NM_003149.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr3:36484941 C>T maps to NM_003149.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:136078014 G>A maps to NM_005862.2 R971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr23:123179181 C>G did not map to a codon.
Sequencing variant TCGA-VP-A87E-01A-31D-A34U-08 chr23:123179075 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99779742 C>T maps to NM_012447.2 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:74072295 A>G maps to NM_213622.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74086400 G>A maps to NM_213622.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr13:33700313 G>A maps to NM_178007.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr23:67937306 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:67937674 C>T did not map to a codon.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr2:191851585 C>T maps to NM_007315.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:40474447 A>G maps to NM_139276.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr17:40476776 G>A maps to NM_139276.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:40362187 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:47755172 A>T maps to NM_001048166.1 C319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X4-A8KS-01A-12D-A364-08 chr1:47746428 C>T maps to NM_001048166.1 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:47735350 G>A maps to NM_001048166.1 N857N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr7:43659291 C>T maps to NM_004760.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:31940214 C>T maps to NM_032454.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:23826530 T>A maps to NM_031414.3 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr4:5500776 C>T maps to NM_018401.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr11:8435221 C>T maps to NM_030906.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:36809555 G>A maps to ENST00000373130 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:62272714 C>T maps to NM_015894.2 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:81864720 C>T maps to NM_033104.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:184931469 G>A maps to NM_020225.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr4:184930875 G>A maps to NM_020225.1 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr15:74472522 G>A maps to ENST00000449139 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:43896962 G>A maps to NM_153700.2 R1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr19:47236331 G>T maps to NM_001039877.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:47231890 C>T maps to NM_001039877.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr23:7223202 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:13256152 G>A maps to NM_003765.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:144508075 G>A maps to NM_003764.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:144508225 C>T maps to NM_003764.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr20:57251291 T>A maps to NM_001001433.1 L308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr11:59559663 C>A maps to NM_004177.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:130438177 T>C maps to NM_003165.3 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:53155476 C>T maps to NM_178509.5 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:147637444 C>A maps to NM_001127715.1 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr3:120976075 G>A maps to NM_014980.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:25288248 C>T maps to NM_014178.6 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:48523738 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:84660506 C>T maps to NM_003849.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:70476260 G>A maps to NM_001128206.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:28631395 C>T maps to NM_177536.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:70721016 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:883101 C>T maps to ENST00000456758 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr22:39134910 C>T maps to ENST00000405018 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr22:39141778 G>A maps to ENST00000405018 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr7:48046773 C>T maps to NM_152782.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31571728 C>T maps to NM_080675.3 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:31575486 C>T maps to NM_080675.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr14:21820849 G>T maps to NM_007192.3 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:39965234 G>T maps to NM_003169.3 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr19:39964092 G>A maps to NM_003169.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HJ-01A-11D-A364-08 chr17:27011734 C>A maps to NM_003170.3 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:70940277 C>T maps to NM_003171.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr10:70940178 C>T maps to NM_003171.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:136199100 C>T maps to NM_006753.4 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr9:136198944 G>A maps to NM_006753.4 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:136200594 G>A maps to NM_006753.4 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr22:24581634 G>A maps to NM_019601.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr3:33216453 G>A maps to NM_015551.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:33194725 C>T maps to NM_015551.1 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88L-01A-11D-A34U-08 chr11:67938485 C>A maps to NM_017635.3 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67925796 G>A maps to NM_017635.3 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:149885320 C>T maps to NM_014849.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr1:149884959 G>A maps to NM_014849.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:149885275 G>A maps to NM_014849.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr1:149885041 C>T maps to NM_014849.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:149879688 G>A maps to NM_014849.3 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:149883425 G>A maps to NM_014849.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:91769873 C>T maps to NM_014848.4 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:75427790 C>T maps to NM_014979.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:75490816 A>G maps to NM_014979.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr9:113312164 C>A maps to ENST00000374463 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:113168744 G>T maps to ENST00000374463 T3048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr9:113231325 G>A maps to ENST00000374463 C1018C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:29819559 G>A maps to NM_021738.2 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:138312092 A>G did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:9746374 T>G maps to NM_015055.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:115454197 C>T maps to NM_003176.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr20:58467115 G>A maps to NM_014258.2 Q765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr6:10928670 C>T maps to NM_001040274.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:15222567 C>T maps to NM_033025.4 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr19:46334799 C>T maps to NM_004819.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:46332277 G>A maps to NM_004819.2 C645C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr3:12187208 G>A maps to NM_133625.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:33260925 T>C maps to NM_003490.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr6:86329032 T>A maps to NM_006372.4 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Y-01A-22D-A32B-08 chr6:86333755 C>A maps to NM_006372.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W1-01A-11D-A377-08 chr6:152754965 C>T maps to NM_182961.2 S1475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:152832184 T>A maps to NM_182961.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr6:152647579 G>A maps to NM_182961.2 N5048N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr6:152469435 C>T maps to NM_182961.2 W8240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr6:152539539 T>C did not map to a codon.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr6:152671419 G>A maps to NM_182961.2 N3928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr6:152711422 G>A maps to NM_182961.2 H2723H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr6:152751619 T>C maps to NM_182961.2 R1562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:152637992 A>G maps to NM_182961.2 I5567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:152674873 C>T maps to NM_182961.2 W3644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:152676012 G>A maps to NM_182961.2 D3569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr6:152847286 G>A maps to NM_182961.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr6:152652493 G>A maps to NM_182961.2 G4442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:64580249 C>T maps to NM_182914.2 D4267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:64532244 C>G maps to NM_182914.2 G3436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr14:64676751 G>A maps to NM_182914.2 T6211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:64497798 C>T maps to NM_182914.2 S2315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:64637026 C>T maps to NM_182914.2 D5694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr22:39770547 C>T maps to NM_004711.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr21:34058197 A>G maps to NM_003895.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr5:150029061 A>C maps to NM_001166209.1 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr5:150029732 G>T maps to NM_001166209.1 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150028073 G>A maps to NM_001166209.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150029258 C>T maps to NM_001166209.1 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:63429126 T>C maps to ENST00000460711 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr17:35945533 G>A maps to NM_007247.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:33529797 G>A maps to NM_198992.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:66812167 C>T maps to NM_001177880.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SR-01B-11D-A377-08 chr11:45265635 C>T maps to NM_020826.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr10:46967542 C>T maps to NM_031912.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJT-01A-11D-A41K-08 chr16:19194988 C>T maps to NM_016524.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr18:40853619 T>A maps to NM_020783.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr19:55687184 C>T maps to NM_003180.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:7334784 G>A maps to NM_175733.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9MC-01A-31D-A41K-08 chr11:7324412 G>T maps to NM_175733.3 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr1:27674031 G>A maps to NM_001193308.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr11:85459456 A>T maps to NM_001162953.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:159129419 C>T maps to ENST00000297239 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:166578322 A>G maps to NM_003181.2 N211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr6:132939002 T>C maps to NM_001033080.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr6:132910498 C>T maps to NM_003967.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:132874313 G>A maps to NM_053278.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr6:132860432 G>A maps to NM_175057.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr22:39826028 G>A maps to NM_006116.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr6:149700268 A>G maps to NM_015093.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:47925337 G>A maps to NM_170685.2 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:38677709 A>G maps to ENST00000379931 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr10:123954656 C>T maps to NM_206862.2 P1979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr10:123843718 A>T maps to NM_206862.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr10:123842617 G>A maps to NM_206862.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:123844900 G>A maps to NM_206862.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:124008245 C>T maps to NM_206862.2 S2827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr4:104640397 G>A maps to NM_001059.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr4:104577478 G>A maps to NM_001059.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:7056102 C>T maps to NM_152293.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:70613198 T>C did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:70613206 A>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr23:70603929 G>A did not map to a codon.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:34147367 C>T maps to NM_139215.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:34171787 T>C maps to NM_139215.1 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:10022927 T>C maps to NM_005680.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr11:93471312 C>A maps to NM_024116.3 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr9:32631137 C>T maps to NM_153809.2 G1480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr1:229738250 G>A maps to NM_014409.3 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr11:62554329 A>T maps to NM_006473.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OT-01A-11D-A41K-08 chr11:62546422 G>A maps to NM_006473.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:100532631 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:100538562 G>A did not map to a codon.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VX-01A-11D-A377-08 chr6:159457440 G>A maps to NM_054114.3 H538H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr3:111719773 G>A maps to NM_001008272.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr9:108425067 G>A maps to NM_005421.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:160050844 C>T maps to NM_033394.2 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr2:160035656 C>G maps to NM_033394.2 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:160035215 C>T maps to NM_033394.2 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr17:61432334 C>A maps to ENST00000389520 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:61492926 C>T maps to ENST00000389520 Y1279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61466674 C>T maps to ENST00000389520 R867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61498025 C>T maps to ENST00000389520 P1571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:61499108 C>T maps to ENST00000389520 P1932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr16:29999003 C>T maps to NM_016151.2 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:29996667 G>A maps to NM_016151.2 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:30002648 G>A maps to NM_004783.2 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32805626 C>T maps to ENST00000452392 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr1:234556447 C>T maps to NM_005646.3 Q1185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:234534275 G>A maps to NM_005646.3 R1365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:234561460 G>A maps to NM_005646.3 H1134H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr7:38305253 G>A maps to ENST00000443402 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:33459801 C>T maps to ENST00000455217 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:150471025 A>G maps to NM_025150.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:6634740 C>A maps to NM_138697.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:9629678 G>A maps to NM_019599.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:11149789 G>A maps to NM_176889.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:11214314 T>A maps to ENST00000422992 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:141490985 G>A maps to NM_018980.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:3567065 G>A maps to NM_014604.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153647887 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr4:38097622 A>G maps to NM_015173.2 V770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:38022222 C>T maps to NM_015173.2 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:30688747 G>A maps to ENST00000403477 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:67173157 G>A maps to NM_198517.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:96162450 C>T maps to NM_015188.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr4:6995921 C>T maps to NM_001113361.1 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:6925364 G>A maps to NM_001113361.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:77926466 G>A maps to NM_019020.2 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr4:26622267 T>A maps to NM_018317.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr4:26622237 T>C maps to NM_018317.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:100971251 G>A maps to NM_018421.3 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATV-01A-11D-A41K-08 chr9:101014205 G>A maps to NM_018421.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:101006408 G>A maps to NM_018421.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr6:37280703 G>C maps to NM_017772.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:48417679 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:48418542 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr6:13316820 C>A maps to NM_016495.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:101656774 G>A maps to NM_001102426.1 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:101644512 G>A maps to NM_001102426.1 N801N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr23:106064138 G>T did not map to a codon.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr5:179296820 G>A maps to NM_198868.2 H913H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:179297285 C>T maps to NM_198868.2 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:179297354 G>T maps to NM_198868.2 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr6:42713802 G>A maps to NM_003192.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:42713703 C>T maps to NM_003192.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:80726351 T>C maps to NM_005993.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:80885100 C>T maps to NM_005993.4 D837D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:80895146 C>T maps to NM_005993.4 D1064D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr1:235597547 C>T maps to NM_003193.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:176755960 C>G did not map to a codon.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr7:72988434 T>A maps to NM_012453.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:2025081 C>T maps to NM_006453.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr6:170871084 G>A maps to NM_003194.4 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr6:170871015 G>A maps to NM_003194.4 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr6:170871045 A>G maps to NM_003194.4 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr6:170871021 G>A maps to NM_003194.4 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr14:55903529 G>A maps to NM_199047.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:119427789 G>A maps to ENST00000369429 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr6:85446894 C>T maps to NM_001080508.1 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr6:85457763 G>A maps to NM_001080508.1 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:85446702 G>A maps to NM_001080508.1 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr6:85466463 G>A maps to NM_001080508.1 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:59560513 G>A maps to ENST00000393853 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr12:114841631 G>A maps to NM_000192.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:3600347 C>T maps to NM_201636.2 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:3600086 C>T maps to NM_201636.2 W182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:3600380 G>A maps to NM_201636.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:23735188 G>T maps to NM_003196.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr23:101381876 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr23:102864067 G>A did not map to a codon.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr23:101395980 C>T did not map to a codon.
Sequencing variant TCGA-KK-A7B3-01A-11D-A33T-08 chr23:101396001 G>A did not map to a codon.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr23:102508605 C>T did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:2827128 C>T did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:24083515 G>T maps to NM_003198.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr1:24075566 G>A maps to NM_003198.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:44559586 G>A maps to NM_016427.2 H683H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr18:44549170 G>A maps to NM_145653.3 Y376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr18:44554577 G>A maps to NM_145653.3 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr5:145890176 C>A maps to NM_006706.3 S1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr5:145834700 C>T maps to NM_006706.3 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WN-01A-11D-A377-08 chr5:145843225 G>A maps to NM_006706.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr15:57484402 A>G maps to NM_207036.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:42610894 A>G maps to NM_005650.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:27372992 C>T maps to NM_175769.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:1615476 C>T maps to NM_003200.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:1612208 G>A maps to NM_001136139.1 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:52899843 G>A maps to ENST00000398339 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr18:52896291 C>T maps to ENST00000398339 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:85510658 C>T maps to NM_031283.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr10:114925328 C>T maps to NM_030756.4 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:114903763 G>A maps to NM_030756.4 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:152082616 G>A maps to NM_007113.2 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr11:67817999 C>T maps to NM_006019.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:149755318 C>T maps to ENST00000451292 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr5:149755038 G>A maps to ENST00000451292 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr6:35089985 G>A maps to NM_001093728.1 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:33080600 C>T maps to NM_001145541.1 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr12:124163787 T>G maps to NM_024809.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:124191585 G>A maps to NM_024809.3 P650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:156825202 C>T maps to NM_005651.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:115982439 C>T maps to NM_198795.1 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:115987858 T>C maps to NM_198795.1 F1171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:179638342 T>C maps to ENST00000444136 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:46656677 C>T maps to NM_001010870.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:46661672 T>C maps to NM_001010870.2 C1936C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:104474748 G>T did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:151748666 C>T maps to NM_001083965.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:151752565 G>A maps to NM_001083965.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr14:102891313 A>T did not map to a codon.
Sequencing variant TCGA-VP-AA1N-01A-31D-A41K-08 chr11:121031010 C>T maps to NM_005422.2 C1619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:120980047 C>T maps to NM_005422.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:120996288 C>T maps to NM_005422.2 H494H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:120996471 C>T maps to NM_005422.2 C555C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:121000864 C>T maps to NM_005422.2 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:27206683 C>T maps to NM_000459.3 D823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr17:15207264 G>A maps to NM_031898.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:1556316 C>T maps to NM_016111.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr14:20847207 G>A maps to NM_007110.4 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:1264628 G>A maps to NM_198253.2 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr10:70446225 G>A maps to NM_030625.2 K1722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74327796 C>T maps to ENST00000409262 P1201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74328450 G>A maps to ENST00000409262 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr9:103092360 C>T maps to NM_017746.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr23:69844761 T>C did not map to a codon.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr23:69843844 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:69749737 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr23:104463751 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr23:104464291 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:104464232 C>A did not map to a codon.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr23:104464699 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr23:107225169 A>G did not map to a codon.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr17:56635170 G>A maps to ENST00000240361 S1482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:30703092 C>T maps to NM_031271.3 Q1147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:30704682 G>A maps to NM_031271.3 D617D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr8:30699597 T>C maps to NM_031271.3 R2312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr15:56657674 G>C maps to NM_198524.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr6:50805732 A>G maps to ENST00000263046 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr1:36055548 G>A maps to NM_178548.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:4310114 C>T maps to NM_003223.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:155581522 G>A maps to NM_016020.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:114288233 C>T maps to NM_007111.4 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr13:114288327 C>T maps to NM_007111.4 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr23:132351391 C>T did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr23:132351871 G>A did not map to a codon.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr23:132351177 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:48891659 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:195782157 A>C maps to NM_001128148.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr3:195800838 C>T maps to NM_001128148.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:133925307 C>T maps to NM_003235.4 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:133920512 C>T maps to NM_003235.4 Y1310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr2:70680365 G>A maps to NM_003236.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr19:41838077 G>A maps to NM_000660.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr16:31485242 C>T maps to NM_001042454.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:218614598 C>T maps to NM_001135599.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:218578520 G>A maps to NM_001135599.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr5:135392371 C>A maps to NM_000358.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:92262993 A>T maps to NM_003243.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:92185485 C>T maps to NM_003243.4 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:92193275 G>A maps to NM_003243.4 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr2:105924086 C>A maps to NM_004257.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:105924479 C>T maps to NM_004257.4 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr24:3447293 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:36767991 G>A maps to NM_004613.2 Y388Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:36770598 G>A maps to NM_004613.2 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr3:44943339 C>T maps to NM_003241.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr20:2380265 C>T maps to NM_198994.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr15:43579552 G>A maps to NM_052955.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RC-01A-11D-A32B-08 chr2:85554632 C>T maps to ENST00000409015 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr2:85554506 C>T maps to ENST00000409015 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:57564938 G>A maps to NM_198976.1 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:43801571 G>A maps to ENST00000330266 Y544Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr22:21354949 T>C maps to NM_030573.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:39883712 C>T maps to NM_003246.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:169629714 G>A maps to NM_003247.2 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:169626361 G>A maps to NM_003247.2 Y817Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYO-01A-11D-A41K-08 chr5:79366953 C>T maps to NM_003248.4 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr19:375679 C>T maps to NM_016585.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:372674 C>T maps to NM_016585.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr6:128134111 C>T maps to NM_001164685.1 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:25312241 G>A maps to NM_024838.4 Q30Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:88478452 G>A maps to NM_018271.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:122761550 T>C did not map to a codon.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr22:29924167 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:63823672 G>A maps to NM_025075.2 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:11630113 G>A maps to ENST00000423059 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:11422232 G>T maps to ENST00000423059 C1474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:11447029 C>T maps to ENST00000423059 W1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr2:137814398 T>G maps to ENST00000272643 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr2:137814554 G>T maps to ENST00000272643 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:137852463 C>T maps to ENST00000272643 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:137917825 G>A maps to ENST00000272643 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:138330059 C>T maps to ENST00000272643 S1122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:39982550 T>A did not map to a codon.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr11:119291594 G>A maps to NM_006288.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:70463279 C>T maps to NM_022173.2 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:155451341 C>T maps to ENST00000456144 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr6:155500567 G>A maps to ENST00000456144 K895K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr1:43779587 C>T maps to NM_005424.2 I786I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr1:43779602 G>T maps to NM_005424.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr4:90034421 A>G maps to NM_145715.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:65123662 A>G maps to NM_145719.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:65124394 G>A maps to NM_145719.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I8-01A-11D-A364-08 chr11:65123572 G>A maps to NM_145719.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:153691370 G>A maps to NM_145720.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr5:156381615 G>A maps to NM_138379.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7318-01B-11D-A32B-08 chr19:2427322 C>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:900588 C>A maps to NM_013337.2 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:7992562 G>A maps to NM_006351.3 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:39979203 C>T maps to NM_001001563.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr6:54216176 C>T maps to NM_014464.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:54186158 G>T maps to NM_014464.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr1:32050622 C>T maps to NM_022164.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:156395882 C>T maps to NM_015508.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:126162648 C>T maps to NM_148910.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:43469375 C>T maps to NM_001146016.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr19:3731955 C>T maps to NM_014428.1 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153524217 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:164393425 T>C maps to NM_032136.4 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr9:84202652 G>T maps to NM_005077.3 V640V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:84208158 A>C maps to NM_005077.3 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:84226743 C>T maps to NM_005077.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:3006489 G>A maps to NM_003260.4 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr15:70352867 C>T did not map to a codon.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr9:82320808 C>T maps to ENST00000376537 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:171862700 A>G maps to ENST00000360843 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:171863308 C>T did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr17:60654068 G>A did not map to a codon.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr17:60601628 T>G maps to ENST00000326270 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr17:60685505 A>G maps to ENST00000326270 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:60685409 C>T maps to ENST00000326270 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr4:167020675 C>T maps to ENST00000507499 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:166996045 T>C maps to ENST00000507499 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:98173003 G>A maps to NM_012465.3 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35700340 G>T maps to NM_006289.3 T2169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35707455 G>A maps to NM_006289.3 N1554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35714816 G>A maps to NM_006289.3 H937H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:35716541 G>A maps to NM_006289.3 R824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:62978868 G>T maps to NM_015059.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:63125773 C>T maps to NM_015059.2 S2358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr4:38798748 C>T maps to NM_003263.3 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:38798901 C>T maps to NM_003263.3 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr9:120475153 C>T maps to NM_138554.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:120475800 C>T maps to NM_138554.3 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:38830344 G>T maps to NM_006068.3 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr23:12904066 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:12903783 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:12904066 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:12906104 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr23:12939903 T>G did not map to a codon.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr23:12938244 C>T did not map to a codon.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr23:12939509 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:102894091 G>A maps to NM_005521.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr10:102849596 G>A maps to NM_001085398.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:74742862 G>A maps to NM_016170.4 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr15:102182732 C>T maps to NM_078474.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr3:149040065 C>A maps to NM_138786.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr3:149192702 C>G maps to NM_004617.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr12:27152540 C>T maps to NM_016551.2 Q105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:105367307 C>T maps to NM_030788.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr14:24661452 C>T maps to NM_006405.5 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr20:30729617 C>A maps to NM_014742.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr9:75445551 T>G maps to NM_138691.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:75407264 A>G maps to NM_138691.2 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:81625593 G>A maps to ENST00000454937 H826H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr19:54667526 C>T maps to NM_001145303.1 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:76113373 G>A maps to NM_007267.6 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:19041571 T>C maps to NM_024847.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr16:19041625 G>A maps to NM_024847.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr16:19020720 G>T maps to NM_024847.3 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87H-01A-11D-A34U-08 chr16:19047012 C>T maps to NM_024847.3 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:205210850 C>T maps to NM_014858.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:94976110 C>T maps to NM_020698.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:140023733 G>A maps to ENST00000252100 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr16:69056742 C>G maps to NM_024562.1 S952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VL-01A-21D-A377-08 chr14:75602589 C>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:177022270 C>T maps to NM_017510.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:193056698 T>C maps to NM_016192.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr2:192863885 G>A maps to NM_016192.2 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr2:192863837 T>C maps to NM_016192.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr2:193059094 G>A maps to NM_016192.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:21101726 G>A maps to NM_003876.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:44338118 G>A maps to NM_032256.1 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:4239661 G>A maps to ENST00000382753 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr7:98460808 G>A maps to NM_001134450.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:98373684 G>T maps to NM_015348.1 P1843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:126138922 C>T maps to NM_052907.2 C968C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83I-01A-11D-A364-08 chr12:130184521 G>A maps to NM_133448.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:32964314 G>A maps to NM_207313.1 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MG-AAMC-01A-11D-A41K-08 chr17:32959838 G>A maps to NM_207313.1 W443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:32964563 C>T maps to NM_207313.1 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:67235039 G>A maps to NM_025124.2 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:120198156 T>C maps to NM_001198670.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr7:134849231 G>A maps to NM_018295.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr19:48845942 C>T maps to NM_018273.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LY-01A-11D-A41K-08 chr19:42821925 G>A maps to ENST00000406159 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr19:5770981 G>A maps to NM_152784.3 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:5751815 C>G maps to NM_152784.3 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr19:55831945 A>G maps to NM_001085488.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr23:109416586 G>C did not map to a codon.
Sequencing variant TCGA-M7-A723-01A-12D-A32B-08 chr2:62728400 C>T maps to NM_198276.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr5:72469162 C>T maps to NM_153217.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:104230505 G>A maps to NM_024789.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr10:104232672 C>T maps to NM_024789.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr6:159046200 G>A maps to NM_020823.1 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SF-01A-11D-A377-08 chr6:159046167 G>A maps to NM_020823.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr2:103431322 C>T maps to NM_144632.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:202984026 C>T maps to NM_001079809.1 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:1587402 G>A maps to NM_001097620.1 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:148555572 C>T maps to NM_018241.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:153248051 G>A did not map to a codon.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr4:166021831 G>T maps to NM_001100389.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:15405838 C>T maps to NM_001004320.1 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:26687827 C>T maps to ENST00000457710 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:95660859 G>A maps to NM_001134658.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:130762196 C>A maps to NM_052913.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:11453675 C>A maps to NM_198536.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr19:11453690 G>T maps to NM_198536.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:25331313 C>A maps to ENST00000423535 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr2:27258871 G>A maps to NM_017727.4 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:63170403 G>T maps to NM_178505.6 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr23:102968707 T>A did not map to a codon.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr3:12783980 A>G maps to ENST00000431022 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr3:12785417 G>A maps to ENST00000431022 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:12791289 A>G maps to ENST00000431022 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr3:100287664 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:129724587 C>T maps to NM_138788.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:54284689 T>C maps to NM_018087.4 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AZ-01A-12D-A32B-08 chr17:57842438 T>G maps to NM_030938.3 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:64173823 C>T maps to NM_014254.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46B-01A-31D-A257-08 chr21:34841165 A>G maps to NM_006134.5 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:15546031 C>T maps to NM_018022.2 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:92033483 C>T maps to NM_018710.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr1:55457538 C>T maps to NM_182532.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:43443999 T>C maps to NM_024956.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:226059716 G>A maps to NM_014698.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr6:44119746 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:29923591 C>T maps to NM_016127.4 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr8:109796598 G>A maps to NM_153015.1 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:18722574 C>T maps to NM_153347.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42523404 A>G maps to ENST00000389834 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:422214 C>T maps to NM_021259.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:425224 G>A maps to NM_021259.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:74876312 G>A maps to NM_001105579.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr20:24524044 C>T maps to NM_024893.1 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr20:24523909 G>A maps to NM_024893.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr3:69075247 C>A maps to NM_007114.2 E920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr3:69087801 A>C maps to NM_007114.2 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr21:19715873 T>C maps to NM_002772.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr21:42839792 C>T maps to NM_001135099.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr21:42866284 G>C maps to NM_001135099.1 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr21:42840427 A>C maps to NM_001135099.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr22:37485724 G>A maps to ENST00000381792 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr19:2421892 C>T maps to NM_182973.1 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr19:2410385 C>A maps to NM_182973.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2408467 C>T maps to NM_182973.1 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr12:83424605 C>T maps to NM_152588.1 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:88568464 T>C maps to NM_181783.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WV-01A-11D-A377-08 chr12:88560142 A>G maps to NM_181783.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:57505472 C>T maps to NM_015959.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:117849132 G>A maps to NM_002160.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A872-01A-11D-A34U-08 chr9:117849181 G>A maps to NM_002160.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:117853141 G>A maps to NM_002160.2 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr17:26666642 C>A maps to NM_021137.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:152220547 C>T maps to NM_007115.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr8:22880192 G>T maps to NM_003842.4 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:22884791 G>A maps to NM_003842.4 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:60021738 C>T maps to NM_003839.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr17:16842992 G>A maps to NM_012452.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:24242128 C>T maps to NM_018647.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:6438669 G>A maps to NM_001065.3 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr12:6440067 C>T maps to NM_001065.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:47200571 C>A maps to NM_014452.3 G633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr5:150444611 G>A maps to NM_006058.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr5:150422162 G>A maps to NM_006058.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:150436422 G>A maps to NM_006058.3 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr4:122075726 A>G maps to ENST00000509841 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr4:122063931 C>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:9413925 T>C maps to NM_003747.2 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr11:57076311 G>A maps to NM_033396.2 A1291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr10:93600427 A>G maps to NM_025235.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr10:93590736 A>C maps to NM_025235.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:175086261 G>A maps to NM_022093.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr1:175054614 C>T maps to NM_022093.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:175105004 C>T maps to NM_022093.1 Q1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XA-A8JR-01A-11D-A364-08 chr11:1860931 A>G maps to ENST00000381906 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr2:217724625 G>A maps to NM_003284.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:72195833 A>G maps to NM_002270.3 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:175372582 G>A maps to NM_003285.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr16:24801363 C>T maps to NM_014494.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:24808869 G>A maps to NM_014494.2 Q1207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:40661214 A>G maps to ENST00000454349 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:76045217 C>T maps to NM_001142640.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr7:47408547 G>A maps to NM_022748.11 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr17:38638447 A>T maps to NM_032865.5 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:32023934 G>T maps to ENST00000375244 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:32021195 G>A maps to ENST00000375244 R2920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr6:32010243 C>G maps to ENST00000375244 G4066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr6:32053653 C>A maps to ENST00000375244 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:32036413 C>T maps to ENST00000375244 G1991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32011640 G>A maps to ENST00000375244 G3805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32029309 G>A maps to ENST00000375244 P2452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:32056718 G>A maps to ENST00000375244 Y874Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr6:32013020 G>A maps to ENST00000375244 T3563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr20:39725935 T>C maps to NM_003286.2 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr8:144398198 G>A maps to NM_052963.1 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr17:38555126 G>T maps to ENST00000357601 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr17:38567941 T>C maps to ENST00000357601 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:38548888 G>A maps to ENST00000357601 D1340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:133342925 T>C maps to NM_007027.3 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr9:32543931 A>C maps to NM_005802.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:32541789 G>A maps to NM_005802.4 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:32543367 G>A maps to NM_005802.4 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr1:179873144 C>T maps to ENST00000398836 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9NI-01A-11D-A41K-08 chr1:179820466 T>A maps to NM_145034.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr8:59728151 C>T maps to NM_014729.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr20:42635233 G>A maps to ENST00000348077 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr16:52484401 C>T maps to ENST00000407228 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VT-01A-11D-A377-08 chr17:7579591 T>C did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr17:7576850 A>C did not map to a codon.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr17:7576926 C>A did not map to a codon.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr15:43701248 G>A maps to NM_001141980.1 R1816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr15:43748752 T>A maps to NM_001141980.1 K685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:43766907 G>A maps to NM_001141980.1 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr8:95952350 C>T maps to NM_033285.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr20:44003690 C>T maps to NM_014477.2 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr3:189586470 G>A maps to NM_003722.4 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr3:189612174 C>T maps to NM_003722.4 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr12:113733847 A>T maps to NM_001143819.1 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr11:68822729 C>A maps to NM_139075.3 Y113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr6:125584047 C>G maps to NM_003287.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr12:72372849 C>T maps to ENST00000389376 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:1488474 C>T maps to NM_000547.5 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y6-A9XI-01A-11D-A41K-08 chr2:1488492 C>T maps to NM_000547.5 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr11:6640070 C>T maps to ENST00000453338 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:6638247 G>A maps to ENST00000453338 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:6640085 G>T maps to ENST00000453338 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:6640449 G>A maps to ENST00000453338 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr13:103297266 G>A maps to ENST00000376052 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:186332112 C>T maps to NM_003292.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr1:186326599 T>C maps to NM_003292.2 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:127298944 C>T maps to NM_001136053.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A875-01A-31D-A34U-08 chr16:1291437 C>T maps to ENST00000461509 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr13:20067610 G>A maps to NM_199254.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:20006631 G>A maps to NM_199254.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:30363691 G>T maps to ENST00000340513 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr7:23556148 T>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50635671 C>T maps to NM_025204.2 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50636540 C>T maps to NM_025204.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr6:111888870 G>A maps to ENST00000340026 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:111880684 G>A maps to ENST00000340026 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:209953927 C>T maps to NM_025228.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:36511684 C>T maps to NM_145803.1 W424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:36516552 G>A maps to NM_145803.1 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2225571 C>T maps to NM_032271.2 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:112572541 C>A maps to NM_006700.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:42264874 G>A maps to NM_001042646.1 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:202245768 G>A maps to NM_015049.2 R748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:118005505 G>A maps to NM_152402.2 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:52400645 T>A did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:36874131 C>T maps to NM_014831.2 L2270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr3:36898224 A>G maps to NM_014831.2 Y952Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr3:36873597 C>A maps to NM_014831.2 L2448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr3:36873536 T>A maps to NM_014831.2 K2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3729743 C>T maps to NM_016292.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3736031 G>A maps to NM_016292.2 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr21:45503101 T>C maps to NM_003274.4 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:118889680 G>A did not map to a codon.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr8:141310580 C>G maps to NM_031466.5 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:141461100 G>A maps to NM_031466.5 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr8:141381087 C>T maps to NM_031466.5 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr6:123600200 G>A maps to NM_006073.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:123600200 G>A maps to NM_006073.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr6:123687295 C>T maps to NM_006073.2 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:118531314 C>T maps to ENST00000264029 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr6:42231117 G>A maps to NM_033502.2 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:42196271 G>A maps to NM_033502.2 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TB-01A-11D-A364-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr12:73056935 C>T maps to NM_013381.2 D1012D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr8:126448346 T>C maps to NM_025195.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr2:12863618 C>T maps to NM_021643.3 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:12880826 C>T maps to NM_021643.3 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr6:30121515 G>A maps to NM_052828.2 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr6:30124742 G>A maps to NM_006778.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:30131520 G>A maps to NM_033229.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:18638607 C>T maps to NM_001037330.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:154215595 C>T maps to NM_015271.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:4411306 G>A maps to NM_003141.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr7:138145409 G>A maps to NM_015905.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr17:54969321 G>A maps to NM_005082.4 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WW-A8ZI-01A-11D-A377-08 chr6:30164319 C>T maps to NM_003449.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr19:59059686 C>G maps to NM_005762.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr19:59060744 G>A maps to NM_005762.2 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:120008220 G>A maps to NM_012101.3 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:120008241 G>A maps to NM_012101.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr11:6479026 G>A maps to NM_033278.2 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr1:115005787 G>A maps to NM_015906.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:114945489 G>A maps to NM_015906.3 C928C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:114968109 C>T maps to NM_015906.3 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr1:114968070 C>T maps to NM_015906.3 Q565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr8:27151800 C>A maps to NM_171982.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:114466494 T>A maps to NM_018700.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr6:30308084 G>A maps to NM_021253.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:140409973 C>T maps to NM_152616.4 Y675Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr1:155147950 C>T maps to NM_025058.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:55036726 C>T maps to ENST00000357530 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:55033096 C>T maps to ENST00000357530 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:89531567 T>C maps to NM_020358.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:89531656 G>A maps to NM_020358.2 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr11:5686408 C>T maps to NM_033034.2 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:5686329 G>A maps to NM_033034.2 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:248039229 G>A maps to NM_015431.3 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr4:165962534 C>G maps to NM_152620.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:165962456 A>G maps to NM_152620.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:33625512 G>A maps to NM_018207.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:73887231 C>T maps to NM_173547.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:231299692 C>T maps to NM_001004342.3 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:231339664 C>T maps to NM_001004342.3 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr10:104414838 G>A maps to NM_030912.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:104416969 G>A maps to NM_030912.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:51446110 G>A maps to ENST00000338969 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr14:51560841 T>A maps to ENST00000338969 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:14504648 C>T maps to NM_007118.2 V2853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:14482806 C>T maps to NM_007118.2 I2194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:14492824 C>T maps to NM_007118.2 A2594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr5:14488269 G>T maps to NM_007118.2 R2511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr22:38121490 C>T maps to NM_001039141.2 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr22:38121844 C>T maps to NM_001039141.2 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr22:38165191 C>T maps to NM_001039141.2 Q2245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38119610 C>T maps to NM_001039141.2 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38119904 C>T maps to NM_001039141.2 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:38131002 C>T maps to NM_001039141.2 R1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SP-01B-11D-A377-08 chr22:38121967 A>G maps to NM_001039141.2 L1135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr19:6750304 G>A maps to ENST00000313244 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr19:6743804 C>T maps to ENST00000313244 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:6743768 C>T maps to ENST00000313244 N188N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr22:20104420 C>T maps to ENST00000439169 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr14:104000980 G>A maps to ENST00000299201 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:28891265 C>T maps to NM_017846.4 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:3178984 G>T maps to NM_182916.2 G64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr23:54957660 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:49721016 C>T maps to NM_005480.3 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:72963063 G>A maps to NM_007332.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr8:72936046 A>G did not map to a codon.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr8:72973924 C>T maps to NM_007332.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:72958762 C>T maps to NM_007332.2 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr8:72973924 C>T maps to NM_007332.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr3:142499732 A>C maps to ENST00000476941 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr13:38213400 T>C maps to NM_003306.1 Q710Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr13:38211513 G>A maps to NM_003306.1 G825G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr23:111156016 C>A did not map to a codon.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr23:111095550 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:135692604 G>A maps to NM_020389.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr15:31294405 G>A maps to NM_002420.4 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:31327751 T>C maps to NM_002420.4 R877R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:73152134 C>T maps to ENST00000419692 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TH-01A-11D-A41K-08 chr19:49692201 G>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:2443515 C>T maps to ENST00000452833 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:77448964 T>C maps to NM_017662.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr9:77390916 G>T maps to NM_017662.4 Y1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:50902041 G>A maps to NM_017672.4 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr8:116632179 C>A maps to NM_014112.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr17:16321002 T>C maps to NM_016113.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr17:3445843 G>A maps to ENST00000381913 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr7:142569696 G>A maps to NM_018646.2 Y647Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:98608823 G>A maps to ENST00000359863 A3682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr7:98513417 T>C maps to ENST00000359863 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:98519494 C>T maps to ENST00000359863 Y914Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr7:98522823 G>T maps to ENST00000359863 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:141952405 A>C maps to NM_001001317.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:141954938 G>A maps to NM_001001317.2 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr7:141955353 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2110815 T>C did not map to a codon.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr13:45148695 T>C maps to NM_183422.2 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:18503233 G>T maps to NM_006292.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr2:99725895 G>A maps to NM_025244.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr7:130357703 G>A maps to NM_052933.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr7:130038877 G>A maps to NM_018718.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr18:73000202 G>A maps to NM_005786.4 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:51870104 C>T maps to NM_173485.5 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:51872366 C>T maps to NM_173485.5 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:31769516 C>T maps to NM_020856.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr19:31770233 G>A maps to NM_020856.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OX-01A-11D-A41K-08 chr19:31768394 G>A maps to NM_020856.2 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:31769228 C>T maps to NM_020856.2 K490K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:50248601 C>T maps to NM_021733.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr19:50245230 G>A maps to NM_021733.1 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TV-01A-11D-A41K-08 chr2:122520660 G>C did not map to a codon.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:67859050 G>T maps to ENST00000339830 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:82264513 C>T maps to NM_030927.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr10:71264231 C>T maps to NM_012339.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:176083708 G>A maps to NM_012171.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:2324132 T>C maps to NM_139022.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:128807690 G>A maps to NM_178562.3 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr23:38540489 G>C did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr12:3390976 C>T maps to ENST00000407263 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:3387723 G>A maps to ENST00000407263 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr24:6114372 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:112769552 G>A maps to NM_032028.3 P328P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5745-01A-11D-1576-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-G9-6366-01A-11D-2114-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19625555 G>A maps to NM_032037.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19625627 G>A maps to NM_032037.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:37407118 G>T maps to NM_003312.4 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144695692 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8SQ-01B-11D-A377-08 chr6:43251408 G>A maps to NM_032538.1 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr5:159476555 T>C maps to NM_003314.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:180324130 C>T maps to NM_133462.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:3461426 C>T maps to NM_016030.5 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr11:43513625 C>T maps to NM_018259.5 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:75029380 G>A maps to NM_145170.3 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:15905278 C>T maps to NM_017775.2 D242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr3:39174616 A>G maps to ENST00000301819 Q887Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QZ-01A-11D-A377-08 chr1:55266617 G>A maps to NM_001114108.1 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:40095413 C>T maps to ENST00000377543 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr4:147628686 G>A maps to ENST00000513335 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr21:38511001 A>C maps to NM_003316.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr2:178481830 A>G maps to NM_152275.3 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:178415724 G>T maps to NM_152517.2 C589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr5:94848277 C>T maps to NM_014639.3 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr22:46685403 G>A maps to NM_017931.2 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:15175096 C>T maps to NM_152574.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr18:21663036 C>T maps to NM_001135993.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr18:21705425 G>T maps to NM_001135993.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:55207180 C>T maps to NM_004623.4 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr2:47278909 C>T maps to ENST00000394850 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr2:47256511 T>A maps to ENST00000394850 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr14:91059905 C>T maps to NM_001010854.1 S677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr14:89307827 A>G maps to NM_144596.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:135275596 G>A maps to NM_007344.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr1:117619326 C>T maps to NM_003594.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I4-01A-11D-A364-08 chr2:113260503 G>A maps to NM_153712.4 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr2:113260631 C>A maps to NM_153712.4 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr22:43460260 G>A maps to NM_012263.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr22:43576900 C>T maps to NM_015140.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:43568520 G>A maps to NM_015140.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr3:9855029 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:9868894 G>A maps to NM_001025930.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:219618907 G>A maps to NM_014640.4 T1132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:76200337 G>A maps to NM_015072.4 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A8O0-01A-41D-A377-08 chr17:46862422 C>T maps to NM_001130918.1 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:84408189 G>A maps to NM_024686.4 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJR-01A-11D-A41K-08 chr22:50488625 A>C maps to NM_001080447.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYF-01A-11D-A41K-08 chr2:179580331 C>T maps to NM_133378.4 S7359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr2:179477936 A>G maps to NM_133378.4 P13965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr2:179585678 G>A maps to NM_133378.4 D6445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr2:179615124 A>C maps to ENST00000375038 L4003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:179440958 C>T maps to NM_133378.4 Q20732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:179399092 T>C maps to NM_133378.4 K31515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr2:179482527 G>A maps to NM_133378.4 F13282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr2:179568877 G>A maps to NM_133378.4 I8829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr2:179412021 G>A maps to NM_133378.4 S28842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179537131 A>G did not map to a codon.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:179456527 A>G maps to NM_133378.4 G17438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr2:179397721 A>T maps to NM_133378.4 Y31972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:179588312 T>G maps to NM_133378.4 R5928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr2:179393600 A>C maps to NM_133378.4 L33058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr2:179432009 T>G maps to NM_133378.4 V23715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr2:179455520 G>A maps to NM_133378.4 R17743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MJ-01A-11D-A364-08 chr2:179403721 C>T maps to NM_133378.4 L30412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr2:179629395 G>A maps to NM_133378.4 G3282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179413763 G>A maps to NM_133378.4 A28295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179478929 C>T maps to NM_133378.4 W13830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179486289 C>T maps to NM_133378.4 L12519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179579943 C>A maps to NM_133378.4 G7413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179591838 G>A maps to NM_133378.4 C5507C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179593389 G>A maps to NM_133378.4 D5177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179594051 G>A maps to NM_133378.4 G5033G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179598395 G>A maps to NM_133378.4 C3996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179623768 C>T maps to NM_133378.4 T3415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179633625 G>A maps to NM_133378.4 N2979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:179641414 G>A maps to NM_133378.4 L1726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:2691854 C>T maps to NM_025250.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:132237010 G>C maps to NM_080386.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr2:132237643 G>A maps to NM_080386.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:130949670 C>T maps to NM_207312.2 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr2:220116306 G>A maps to NM_006000.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr16:89999981 C>T maps to ENST00000304984 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr19:6495441 G>A maps to NM_006087.2 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr19:6496110 G>A maps to NM_006087.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:40811927 C>T maps to NM_016437.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:135098973 C>T maps to NM_006659.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:43693985 C>T maps to ENST00000399460 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr15:43669216 G>A maps to ENST00000399460 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr15:22851078 T>G maps to NM_052903.4 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr22:50682159 C>A maps to NM_020461.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr22:50682699 T>C maps to NM_020461.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:28854381 G>A maps to NM_003321.4 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:35471597 C>T maps to NM_003322.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:158870173 C>T maps to NM_020245.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr17:1183348 C>T maps to NM_172367.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr7:19738112 C>T maps to NM_001002926.1 K281K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:32660567 C>T maps to NM_175852.3 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr23:16859874 G>C did not map to a codon.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:11785488 G>A maps to ENST00000356957 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:134223830 G>T maps to NM_024715.3 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:52957170 T>C did not map to a codon.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr14:52936857 C>G maps to NM_020784.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr18:9888098 T>G maps to NM_001098529.1 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:145441199 C>T maps to NM_006472.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:145439909 T>C maps to NM_006472.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr18:54291517 C>A did not map to a codon.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr22:19903311 G>A maps to NM_006440.3 C168C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr19:10468471 C>A maps to NM_003331.4 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr19:10464233 C>T maps to NM_003331.4 Q999Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:10468706 G>A maps to NM_003331.4 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7312-01B-21D-A32B-08 chr11:88911726 T>C maps to NM_000372.4 H202H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:89028438 C>T maps to NM_000372.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr7:66489942 G>A maps to NM_018264.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:66479424 G>A maps to NM_018264.2 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr7:72081821 G>A maps to NM_001145440.1 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:72040530 G>A maps to NM_001145440.1 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr21:44514889 A>G maps to NM_001025203.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr9:139975260 G>A maps to NM_207309.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr23:47069465 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:47061765 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:34942994 G>A maps to NM_005499.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:68543397 G>A maps to NM_018227.5 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr9:33943521 C>A maps to NM_018449.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr21:43829692 C>T maps to NM_018961.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr11:122659911 C>T maps to NM_032873.4 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:122680578 C>A maps to NM_032873.4 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr17:16285496 A>G maps to NM_018955.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr17:16285490 C>T maps to NM_018955.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SU-A7E7-01A-22D-A33T-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:125398089 C>T maps to NM_021009.5 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WS-01A-11D-A377-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:103720583 G>T maps to NM_181890.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:1365671 C>T maps to NM_194259.1 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr17:74396559 G>A maps to NM_022066.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:74392305 G>A maps to NM_022066.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74387398 C>T maps to NM_022066.3 S1168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:64698333 T>C did not map to a codon.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr15:25605554 C>T maps to NM_000462.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:10231329 G>A maps to NM_001105562.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:10231365 G>A maps to NM_001105562.2 A1168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr16:23578314 T>C maps to ENST00000219638 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr23:56591152 G>A did not map to a codon.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr11:5529390 T>C maps to NM_017481.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DX-01A-11D-A377-08 chr11:5530164 C>T maps to NM_017481.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I6-01A-11D-A364-08 chr11:5537356 G>A maps to NM_145053.4 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr6:42600571 G>A maps to NM_015255.2 W492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:170938347 C>T maps to ENST00000442603 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:170929969 C>T maps to ENST00000442603 C1713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr1:19481548 C>T maps to ENST00000375267 A2107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:19403306 G>T maps to ENST00000375267 A5159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83M-01A-11D-A34U-08 chr1:19480293 G>A maps to ENST00000375267 Q2200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr8:103298846 T>C did not map to a codon.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr8:103291367 G>A maps to NM_015902.4 R2024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr14:93684960 G>A maps to NM_175748.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:42293126 G>A maps to NM_014233.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FS-01A-11D-A34U-08 chr1:26608891 G>A maps to NM_183008.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr8:59343159 G>T maps to NM_001077619.1 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr2:136527362 G>A maps to NM_014607.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr3:196089431 C>A maps to NM_015562.1 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr20:62572024 G>A maps to NM_017859.3 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:18579844 G>C maps to NM_001040697.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:19455393 A>G did not map to a codon.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr4:186329109 C>T maps to NM_018359.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr4:39522979 A>G maps to NM_003359.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr2:234527190 G>T maps to NM_019076.4 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr4:69693266 G>A did not map to a codon.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr4:69696452 C>T maps to NM_001075.4 N481N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A9TE-01A-11D-A41K-08 chr4:70080377 C>T maps to NM_001073.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:70152507 T>C maps to NM_053039.1 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr4:70361504 C>T maps to NM_021139.2 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr4:69962450 T>C maps to NM_001074.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:36039600 C>T maps to NM_174914.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:162469883 G>A maps to NM_175866.4 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:4929358 C>T maps to ENST00000398240 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:34804090 G>T maps to NM_017754.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:34824187 T>C did not map to a codon.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr12:100452767 A>G maps to NM_015054.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:100433474 G>A maps to NM_015054.1 Q1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:100452720 C>T maps to NM_015054.1 E778E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr12:100492186 T>C maps to NM_015054.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr9:6504675 C>T maps to NM_152896.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4L-AA1F-01A-11D-A41K-08 chr6:150289966 C>T maps to NM_025218.2 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:150267637 G>A maps to NM_025217.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:19699556 A>T maps to NM_014683.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:19705102 T>C maps to NM_014683.3 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr15:54306248 C>G maps to ENST00000260323 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr15:54804027 G>A maps to ENST00000260323 E1819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:54792333 A>G maps to ENST00000260323 E1706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A71Z-01A-12D-A32B-08 chr15:54306845 G>A maps to ENST00000260323 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr15:54847664 G>A maps to ENST00000260323 T1971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr17:73836862 C>T maps to ENST00000412096 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr17:73836335 G>A maps to ENST00000412096 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:73055701 G>A maps to NM_170744.3 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:96106266 G>A maps to NM_003728.3 H739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8X3-01A-11D-A377-08 chr8:35406945 C>T maps to ENST00000416672 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:35647891 C>T maps to ENST00000416672 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18971712 C>T maps to ENST00000418384 I804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:18976953 G>A maps to ENST00000418384 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:48147887 C>T maps to NM_003364.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr22:30163413 A>G maps to ENST00000406782 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr8:97243339 C>T maps to NM_006294.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IJ-01A-11D-A34U-08 chr1:229773317 T>A maps to NM_014777.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:43916457 G>A maps to NM_001077663.1 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LS-01A-12D-A41K-08 chr3:126208212 C>T maps to NM_001165974.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NF-01A-11D-A33T-08 chr19:17330465 G>A maps to NM_018467.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A9DI-01A-11D-A377-08 chr19:35761490 C>T maps to NM_003367.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:72916330 C>T maps to NM_173477.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:216052410 G>A maps to ENST00000366943 N2751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NN-01A-11D-A33T-08 chr1:216011337 A>G maps to ENST00000366943 T3122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CM-01A-11D-A34U-08 chr1:216256914 A>T maps to ENST00000366943 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:215813956 G>A maps to ENST00000366943 R4971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:215848229 G>A maps to ENST00000366943 C4341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:216074110 G>A maps to ENST00000366943 T2479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:216371663 T>C maps to ENST00000366943 G1358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L6-01A-11D-A41K-08 chr1:216138761 T>C maps to ENST00000366943 T2339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr1:215956214 G>A maps to ENST00000366943 R3484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr19:17370704 C>T did not map to a codon.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr19:17374838 C>A maps to NM_031941.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D1-01A-11D-A364-08 chr16:84778362 C>T maps to NM_005153.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr23:47099250 G>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr13:27649443 T>A maps to NM_182488.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:198099 C>T maps to NM_005151.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr12:62777655 A>G maps to ENST00000280377 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr21:30415787 G>T maps to NM_006447.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr11:119228894 G>A maps to NM_004205.4 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:119243941 G>A maps to NM_004205.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr17:20910261 G>A maps to ENST00000455117 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76X-01A-11D-A33T-08 chr17:20922441 T>A maps to ENST00000455117 K227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:20924446 G>A maps to ENST00000455117 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr23:132159946 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr11:113704217 G>C maps to NM_020886.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr11:113711418 C>T maps to NM_020886.2 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:113675463 G>A maps to NM_020886.2 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:113683226 C>T did not map to a codon.
Sequencing variant TCGA-M7-A723-01A-12D-A32B-08 chr19:57641659 T>G maps to NM_020903.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB20-01A-12D-A41K-08 chr15:63824849 C>T maps to NM_006537.2 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr12:109523651 G>T maps to NM_032663.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AW-01A-11D-A32B-08 chr16:23079699 C>T maps to NM_020718.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr16:23080593 G>A maps to NM_020718.3 V944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:78194271 G>A maps to NM_015017.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:61463361 C>T maps to NM_014709.3 W2284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:61575065 G>A maps to NM_014709.3 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr11:77917054 C>T maps to NM_020798.2 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:77911273 C>T maps to NM_020798.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:77924825 C>T maps to NM_020798.2 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr17:76803038 A>C did not map to a codon.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:219353101 G>T maps to NM_020935.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:144136035 C>T maps to NM_032557.5 D969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr7:6187372 C>T maps to ENST00000404835 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83L-01A-11D-A34U-08 chr6:99936562 G>C maps to NM_001080481.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr11:11969589 C>A maps to ENST00000399455 R1071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:11913564 G>A maps to ENST00000399455 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr11:11963958 G>A maps to ENST00000399455 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:41774067 G>A maps to ENST00000373009 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr6:41773968 G>A maps to ENST00000373009 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr12:6964974 G>A maps to NM_001098536.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr15:50833425 T>C maps to ENST00000456636 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:75277321 C>T maps to NM_152586.3 K954K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:5033902 C>T maps to NM_004505.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:5042865 C>T maps to NM_004505.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:11505705 C>T maps to NM_001080491.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:9017177 G>A maps to NM_003470.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr15:50790906 T>C maps to NM_005154.3 Y1051Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr23:41000650 G>A did not map to a codon.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr23:40999969 A>G did not map to a codon.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr23:41075903 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:41029389 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8SL-01B-21D-A377-08 chr23:41082489 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr23:40988336 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr24:14924837 C>T did not map to a codon.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr13:52603569 T>C maps to NM_021645.5 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:101764853 C>T maps to NM_014503.2 L2236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr12:101766715 T>C maps to NM_014503.2 L2285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:101763626 C>T maps to NM_014503.2 A2171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr8:117783945 T>A maps to NM_032334.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:145093096 A>G maps to NM_007124.2 Q2850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr6:144783989 C>T maps to NM_007124.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr6:144837471 T>C maps to NM_007124.2 N1784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:144999597 C>T maps to NM_007124.2 N2512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr16:70818708 G>A maps to NM_018052.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:85818985 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:85818894 G>A maps to NM_006634.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr23:155119201 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:155169448 G>A did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr1:160394000 G>A maps to NM_020335.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr1:160395041 A>G maps to NM_020335.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:160389120 G>A maps to NM_020335.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L5-01A-12D-A41K-08 chr1:160388964 G>A maps to NM_020335.2 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:30882961 G>A maps to NM_001167734.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr19:46020998 G>T maps to NM_003370.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr16:77859292 C>T maps to NM_020927.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AP-01A-12D-A33T-08 chr19:6850725 A>C maps to NM_005428.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr19:6854099 C>A maps to NM_005428.2 I825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:136641199 C>T maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:108247661 A>G maps to NM_006113.4 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr1:108231001 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:118891814 T>C did not map to a codon.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr1:101198103 C>T maps to NM_001078.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:101198115 G>A maps to NM_001078.3 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:82808054 C>T maps to NM_004385.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr5:82815918 G>A maps to NM_004385.4 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IM-01A-11D-A364-08 chr5:82837392 T>A maps to NM_004385.4 S2857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9ND-01A-11D-A41K-08 chr10:75843161 G>T maps to NM_014000.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr8:67579178 C>A maps to NM_025054.4 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A8FN-01A-11D-A34U-08 chr23:7811725 A>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:48251319 G>A maps to NM_001017535.1 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:43748502 C>T maps to NM_001025366.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr4:177713363 G>A maps to NM_005429.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:156983434 G>A maps to NM_001167912.1 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:100807836 G>A maps to NM_003378.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr6:117589487 A>C maps to NM_182645.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:87018022 G>A maps to NM_016206.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:10191468 A>G did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:38038578 C>A maps to NM_015873.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr14:77908978 G>A maps to ENST00000445370 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:42572368 C>T maps to NM_004624.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr3:42569560 C>A maps to NM_004624.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:37035643 G>A maps to NM_053276.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:51456179 G>A maps to ENST00000273612 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:22599403 G>A maps to NM_007128.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr11:118949954 C>A maps to NM_021729.4 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr9:80022519 C>A maps to ENST00000376646 A3158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:79898328 G>A maps to ENST00000376646 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:79875064 G>A maps to ENST00000376646 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr8:100866332 C>T maps to NM_017890.3 V3597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr8:100866041 A>G maps to NM_017890.3 K3500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr15:62320581 G>A maps to NM_020821.2 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:12336132 C>T maps to NM_015378.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:12460320 C>T maps to NM_015378.2 T3906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:12337556 G>A maps to NM_015378.2 T1304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:12371651 G>A maps to NM_015378.2 R2264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:12416056 C>T maps to NM_015378.2 Q3261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr20:2842495 G>A maps to NM_022575.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr20:2843244 C>T maps to NM_022575.2 D364D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr15:41192239 C>T maps to NM_020857.2 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83G-01A-11D-A34U-08 chr2:86790450 G>C maps to NM_016079.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:70917883 C>A maps to NM_004896.3 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr8:145649502 G>A maps to NM_183057.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:91549290 T>A did not map to a codon.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr15:42456580 C>T maps to ENST00000348544 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr7:38807199 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:38791804 G>A maps to NM_014396.3 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:33236869 G>A maps to NM_022553.4 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:33236314 G>A maps to NM_022553.4 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr2:64211106 T>G maps to NM_016516.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:97322894 C>T maps to NM_003384.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr23:65252420 T>C did not map to a codon.
Sequencing variant TCGA-YL-A8SJ-01B-11D-A377-08 chr2:17830729 C>T maps to NM_003385.4 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr1:117695922 G>A maps to NM_024626.2 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B2-01A-12D-A32B-08 chr2:98736172 A>G maps to NM_144992.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr7:49951736 G>T maps to NM_198570.3 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:61034969 C>T maps to NM_152718.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:6172164 C>T maps to NM_000552.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:6125267 G>A maps to NM_000552.3 A1814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:6161935 C>T maps to NM_000552.3 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr10:28822944 G>A maps to NM_016628.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WL-01A-11D-A377-08 chr10:88260093 C>T maps to ENST00000342368 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:119576826 G>A maps to NM_015836.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr23:48547129 G>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:27755319 G>A maps to NM_006990.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr12:14940328 C>A maps to NM_016312.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:42423016 C>A maps to NM_152613.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr7:73112191 C>G maps to ENST00000423497 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr4:85699757 G>A maps to NM_014991.4 I1472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:85738567 G>A maps to NM_014991.4 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:55474014 G>A maps to NM_007086.3 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:55493427 C>T did not map to a codon.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr10:122662579 G>T maps to NM_018117.11 E923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:203760880 C>T maps to NM_018256.3 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAK1-01A-11D-A41K-08 chr23:48462708 G>A did not map to a codon.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr23:48458009 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:9489196 C>T maps to NM_145054.4 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:989794 C>T maps to NM_024100.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:990901 G>A maps to NM_024100.3 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr4:39230259 G>T maps to NM_025132.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr14:102675208 C>T maps to ENST00000454394 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:100950457 C>T maps to NM_001161476.1 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:118479417 G>T maps to NM_006784.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B0-01A-11D-A32B-08 chr1:118486063 C>T maps to NM_006784.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:116082636 C>T maps to NM_001012361.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr9:116079079 G>C maps to NM_001012361.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr2:128476955 G>A maps to NM_018383.4 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:128477098 G>A maps to NM_018383.4 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:20135318 G>A maps to NM_001006657.1 R831R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:110434430 C>A maps to NM_139281.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:110446961 C>T maps to NM_139281.2 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:29148006 T>G maps to NM_015131.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I7-01A-21D-A364-08 chr23:117532359 G>A did not map to a codon.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr3:167217985 C>A maps to NM_178824.3 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:167293927 G>T maps to NM_178824.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:137023094 C>T maps to NM_052821.3 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:113152409 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:36594431 C>T maps to NM_001083961.1 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:85589837 C>T maps to NM_145172.3 D672D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:85551599 C>A maps to NM_145172.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:43672497 C>T maps to NM_001195831.1 C550C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr12:122441612 C>T maps to NM_144668.4 F1131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:122359384 C>T maps to NM_144668.4 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:124089434 C>T maps to NM_145647.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:54591237 G>A maps to NM_015285.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr18:54547244 C>A maps to NM_015285.2 T1125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr18:54547217 T>C maps to NM_015285.2 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr5:37379472 G>T maps to NM_018034.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:53998223 C>T maps to NM_182758.2 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr15:54015096 C>T maps to NM_182758.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr15:85189498 A>G maps to NM_032856.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:111983959 C>T maps to NM_024102.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8D0-01A-11D-A364-08 chr1:67299305 G>A maps to NM_024763.4 R659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:3551599 C>A maps to NM_017818.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJA-01A-11D-A41K-08 chr1:3548111 C>T maps to NM_017818.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:1637343 C>T maps to NM_001163809.1 T1671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr3:52304794 A>G maps to NM_025222.3 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr16:703784 G>A maps to NM_145294.4 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:134889021 G>A maps to NM_014149.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:27630136 C>T maps to ENST00000319394 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr20:44167962 G>A maps to ENST00000372665 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:6302430 G>A maps to NM_006005.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr4:6302391 G>A maps to NM_006005.3 K290K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr4:1980395 C>T maps to NM_133335.3 D1286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NG-01A-31D-A33T-08 chr4:1902917 G>A maps to NM_133335.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:1961235 G>A maps to NM_133335.3 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr8:38157096 G>A maps to NM_023034.1 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-AAU2-01A-11D-A41K-08 chr8:38173510 G>A maps to NM_023034.1 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr8:38205426 G>C maps to NM_023034.1 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr12:65461529 A>G maps to NM_007191.4 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:29927786 G>A maps to NM_001080529.1 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr17:66440640 G>A maps to NM_017983.5 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr20:43355878 G>A maps to NM_003881.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:15535751 G>A maps to ENST00000389282 G1424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr12:993362 C>T maps to NM_001184985.1 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr23:54359993 C>T did not map to a codon.
Sequencing variant TCGA-KK-A8IF-01A-11D-A364-08 chr23:54259321 C>T did not map to a codon.
Sequencing variant TCGA-V1-A9O5-01A-11D-A41K-08 chr23:54276006 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:54359608 G>A did not map to a codon.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr12:49374246 C>T maps to NM_005430.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:219746966 C>T maps to NM_025216.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:113057603 C>T maps to NM_024494.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:228210433 G>A maps to ENST00000366753 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr1:228238396 C>T maps to ENST00000366753 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:55504239 G>A maps to NM_003392.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr2:219735844 G>A maps to NM_006522.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:219738491 G>A maps to NM_006522.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr3:13896274 G>A maps to NM_004625.3 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:13916636 G>A maps to NM_004625.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr22:46319176 G>A maps to NM_058238.2 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr8:30958413 G>A maps to NM_000553.4 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr8:31015024 C>A maps to NM_000553.4 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:30958413 G>A maps to NM_000553.4 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:31007865 G>A maps to NM_000553.4 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr6:2770370 C>T maps to NM_020135.2 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr12:118474219 G>C maps to ENST00000441406 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr12:108603945 C>T maps to ENST00000261400 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr12:108604002 C>T maps to ENST00000261400 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:32413577 G>A maps to NM_024426.4 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:32417838 G>A maps to NM_024426.4 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:34984202 C>T maps to ENST00000270288 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:167798440 G>A maps to NM_001161661.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr23:10058809 G>A did not map to a codon.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr16:78466399 C>T maps to NM_016373.1 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:78143684 C>T maps to NM_016373.1 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr8:87470209 C>T maps to NM_007013.3 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:69965458 G>A maps to NM_007014.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:7691146 C>A maps to NM_020196.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:6673969 T>C maps to NM_017523.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TK-A8OK-01A-22D-A364-08 chr22:29195089 A>C maps to ENST00000403532 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr1:168510201 G>A maps to NM_003175.3 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83N-01A-11D-A34U-08 chr2:31604514 C>T maps to NM_000379.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr2:31562435 C>T maps to NM_000379.3 P1231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:31611155 A>G maps to NM_000379.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr23:2726250 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:39229796 G>A maps to NM_194293.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:168099281 T>G maps to NM_152381.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8MM-01A-11D-A377-08 chr2:168100850 C>T maps to NM_152381.5 F983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z8-01A-11D-A41K-08 chr2:168104429 C>T maps to NM_152381.5 Y2176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr2:168067308 T>A maps to NM_152381.5 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:168074806 G>A maps to NM_152381.5 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:168103286 G>A maps to NM_152381.5 R1795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:168106836 C>T maps to NM_152381.5 L2979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr23:37553557 A>G did not map to a codon.
Sequencing variant TCGA-V1-A9ZI-01A-11D-A41K-08 chr22:17280820 C>T maps to NM_175878.3 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30584458 C>T maps to NM_001011718.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr9:100447234 T>A maps to NM_000380.3 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:14214485 G>A maps to NM_004628.4 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr23:128901597 C>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:128896710 G>A did not map to a codon.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:128894499 C>T did not map to a codon.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr13:21401282 G>A maps to NM_022459.4 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr13:21436892 G>T maps to NM_022459.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr8:21833902 C>T maps to ENST00000434536 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr8:21842351 T>A did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:180793907 A>T maps to NM_004736.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O7-01A-21D-A41K-08 chr7:152373124 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr5:82499424 G>T maps to NM_022406.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr22:42042989 C>T maps to NM_001469.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:142137377 G>A maps to NM_019001.3 Y438Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:38408365 T>C did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr16:17294397 G>A maps to NM_022166.3 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:48431802 C>T maps to NM_022167.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr12:32903752 G>A maps to NM_001040436.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LB-01A-11D-A41K-08 chr1:43162924 A>C maps to NM_004559.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr3:183521929 C>T maps to NM_018023.4 D1246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:183508766 C>T maps to NM_018023.4 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr23:67731783 A>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:19645850 G>A maps to NM_198537.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:75264384 C>T maps to NM_019589.2 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr10:27412530 G>A maps to NM_139312.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:27423039 G>A maps to NM_139312.1 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:69198539 T>C maps to NM_001031732.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-AAYU-01A-11D-A41K-08 chr5:112878168 C>T maps to NM_022828.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr5:112876725 T>C maps to NM_022828.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr5:112889506 C>T maps to NM_022828.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:61834853 C>T maps to NM_017798.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:43530231 C>T maps to NM_139323.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:9731519 C>T did not map to a codon.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr23:21875523 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:74077645 G>A maps to NM_180990.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:100350274 A>G maps to ENST00000349350 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr7:100348485 C>A maps to ENST00000349350 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr7:100363149 C>T maps to ENST00000349350 C1481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I5-01A-11D-A364-08 chr7:100371058 C>A maps to ENST00000349350 T1859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:100392852 G>A maps to ENST00000349350 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr2:98351130 C>T maps to NM_001079.3 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:98340696 C>T maps to NM_001079.3 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr3:167000275 T>C maps to ENST00000307529 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr3:167045901 T>C maps to ENST00000307529 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr23:2407935 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IG-01A-11D-A364-08 chr23:2407292 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:2407777 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:2407907 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:50279586 G>A maps to NM_014838.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:56185391 C>T maps to NM_030776.2 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr3:101384240 G>C maps to NM_014415.3 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NH-01A-12D-A33T-08 chr6:31868518 T>C maps to NM_181842.2 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:16269096 G>A maps to ENST00000375733 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:151686670 G>A maps to NM_020861.1 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr6:151687731 G>A maps to NM_020861.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:151686670 G>A maps to NM_020861.1 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr6:33284251 G>A maps to NM_001145338.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr9:129642272 C>T maps to ENST00000319119 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr12:57397204 C>T maps to NM_014830.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:7367124 C>T maps to NM_020899.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr1:197169425 G>A maps to NM_194314.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr9:129595972 C>T maps to NM_014007.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:129595901 C>T maps to NM_014007.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IL-01A-11D-A364-08 chr11:130109741 C>T maps to ENST00000397753 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr20:62384050 C>T maps to NM_025224.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr3:42704606 G>A maps to NM_145166.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr19:4054987 G>A maps to NM_015898.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:4048172 G>A maps to NM_015898.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr1:154988263 C>T maps to ENST00000417934 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:33423632 A>G maps to NM_152735.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9M4-01A-11D-A41K-08 chr6:33423654 C>T maps to NM_152735.3 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203819751 G>A maps to NM_014827.4 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8ML-01A-11D-A377-08 chr23:64722773 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:64722866 C>T did not map to a codon.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr13:46577301 G>A maps to ENST00000242848 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr16:88688649 G>C maps to ENST00000452588 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr16:88688650 C>T maps to ENST00000452588 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:144620918 G>A maps to NM_015117.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:138749721 G>A maps to ENST00000464606 N754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr1:52941094 C>G maps to NM_001009881.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr23:117959281 G>A did not map to a codon.
Sequencing variant TCGA-J4-AATZ-01A-11D-A41K-08 chr23:117959897 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:117959423 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:117959681 G>A did not map to a codon.
Sequencing variant TCGA-KK-A8IH-01A-11D-A364-08 chr16:87451281 C>T maps to NM_015144.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:87446013 A>G maps to NM_015144.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QY-01A-11D-A377-08 chr16:87452472 G>C maps to NM_015144.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr23:111698032 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:60241836 C>T maps to NM_017742.4 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr23:77913570 G>A did not map to a codon.
Sequencing variant TCGA-KK-A7B1-01A-11D-A32B-08 chr23:77912604 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:77912929 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:77913289 G>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:88924392 A>G maps to NM_024617.3 I1189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr9:37304307 C>T maps to NM_032226.2 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr12:122958559 G>A maps to NM_017612.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99998765 G>A maps to NM_017984.3 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr2:207175935 G>A maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:207175941 C>T maps to NM_020923.1 Y2230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:67429018 C>T maps to NM_013304.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr12:77202834 G>A maps to NM_015336.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:77244671 C>T maps to NM_015336.2 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8ID-01A-11D-A364-08 chr3:195925261 C>T maps to NM_001039617.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:85015548 G>A maps to NM_001145548.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87B-01A-11D-A34U-08 chr23:128944943 C>T did not map to a codon.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr10:31809235 C>T maps to NM_001174096.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:31815670 C>T maps to NM_001174096.1 R953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:145156430 A>G maps to NM_014795.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F3-01A-21D-A33T-08 chr2:145157535 T>C maps to NM_014795.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:145147500 G>T maps to NM_014795.3 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:145274890 G>A maps to NM_014795.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr9:131503067 C>T maps to NM_006336.2 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A879-01A-11D-A34U-08 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:1192811 G>A maps to ENST00000401903 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr8:135612747 G>A maps to NM_020863.3 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87J-01A-11D-A34U-08 chr8:135614922 G>A maps to NM_020863.3 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:135524783 C>A maps to NM_020863.3 E1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:135649892 C>A maps to NM_020863.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:72036213 A>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:72056883 C>T maps to NM_144982.4 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr16:72991391 G>A maps to NM_006885.3 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr16:72845537 G>A maps to NM_006885.3 Q1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:72829830 C>T maps to NM_006885.3 T2250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OL-01A-11D-A41K-08 chr16:72984598 G>C maps to NM_006885.3 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr16:72832433 C>A maps to NM_006885.3 E1383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr16:72828629 C>A maps to NM_006885.3 E2651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:77764256 C>T maps to NM_024721.4 H1700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:77617576 C>A maps to NM_024721.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:77766737 G>A maps to NM_024721.4 P2527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9Z9-01A-21D-A41K-08 chr8:77765580 A>T maps to NM_024721.4 K2142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr8:77767001 A>G maps to NM_024721.4 E2615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CP-01A-11D-A34U-08 chr15:42720230 G>T maps to NM_022473.1 V1638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42740532 G>A maps to NM_022473.1 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr15:42740884 T>C maps to NM_022473.1 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44831639 C>T maps to ENST00000412927 K907K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:57065113 G>A maps to NM_020828.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr19:57065053 C>G maps to NM_020828.1 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:57065051 G>C did not map to a codon.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr19:39899002 C>G maps to NM_003407.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:43452135 C>T maps to NM_006887.4 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L9-01A-11D-A41K-08 chr6:29640807 G>T maps to NM_001109809.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr20:50769704 A>T maps to NM_018197.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87D-01A-11D-A34U-08 chr20:50803476 G>A maps to NM_018197.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:68591959 C>T maps to NM_133458.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:68597346 C>A maps to NM_133458.2 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:68597460 C>T maps to NM_133458.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7325-01B-11D-A32B-08 chr8:106813674 G>A maps to NM_012082.3 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr8:106813419 C>T maps to NM_012082.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:106814358 C>T maps to NM_012082.3 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:106814721 G>A maps to NM_012082.3 T804T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:3833722 C>T maps to NM_015174.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:24225494 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:24229487 C>T did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr14:73459967 C>T maps to NM_021260.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:15127454 G>A maps to NM_022340.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr14:68220895 C>A maps to NM_015346.3 V2340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:2273483 C>T maps to NM_020972.2 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr8:124267244 A>G maps to NM_007222.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr8:123965723 C>T maps to NM_014943.3 Y658Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr20:39832182 G>A maps to NM_015035.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr3:147128792 C>T maps to NM_003412.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IA-01A-11D-A364-08 chr3:147128234 G>A maps to NM_003412.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IK-01A-11D-A364-08 chr3:147128056 C>A maps to NM_003412.3 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:147131196 C>T maps to NM_003412.3 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr13:100635172 A>G maps to NM_007129.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9O9-01A-11D-A41K-08 chr23:136651108 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:136649561 G>A did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr13:100622585 C>T maps to NM_033132.3 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:58101496 C>T maps to NM_001010879.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr19:57301239 C>T maps to NM_001146326.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:99631795 C>T maps to NM_003439.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:25251247 G>T maps to NM_001012981.4 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99129370 C>T maps to NM_014569.3 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:81050915 C>T maps to NM_020338.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:81056319 C>A maps to NM_020338.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:81060602 C>T maps to NM_020338.3 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A721-01A-12D-A32B-08 chr7:44801485 C>G maps to NM_031449.3 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44796658 G>A maps to NM_031449.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44799757 G>A maps to NM_031449.3 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:44800043 C>T maps to NM_031449.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WY-01A-11D-A41K-08 chr7:44799775 C>T maps to NM_031449.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:35579020 A>G maps to NM_024772.3 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:35579044 C>T maps to NM_024772.3 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr23:70471026 C>A did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr23:70461109 G>C did not map to a codon.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr23:70461110 G>T did not map to a codon.
Sequencing variant TCGA-HC-A76W-01A-11D-A33T-08 chr23:70462904 G>C did not map to a codon.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr23:70462163 A>C did not map to a codon.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr23:70465272 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:70471080 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr23:70461116 G>A did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:35884162 C>T maps to NM_005095.2 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:45867670 C>T maps to ENST00000471951 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr19:19790541 T>C maps to NM_033204.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr7:64438886 A>G maps to NM_015852.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88K-01A-11D-A34U-08 chr5:43175081 C>T maps to ENST00000509156 N573N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr12:133683236 A>C maps to NM_003440.2 *458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr4:367132 C>T maps to NM_003441.2 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr2:219507892 C>A maps to NM_001105537.1 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:219503082 G>A maps to NM_001105537.1 P1681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr2:219508076 G>A maps to NM_001105537.1 G1054G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:9492876 C>T maps to NM_003442.5 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr19:36728179 A>T maps to NM_007145.2 K280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:58213659 A>G maps to NM_001085384.1 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47271770 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47271774 C>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47272238 C>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47272264 C>T did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47272504 C>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47272568 C>A did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47272588 C>G did not map to a codon.
Sequencing variant TCGA-ZG-A9LN-01A-11D-A41K-08 chr23:47272697 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:146157094 G>A maps to NM_006958.2 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:53572739 G>T maps to NM_001102603.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88R-01A-11D-A364-08 chr3:44611915 C>G maps to NM_018651.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44980969 C>T maps to NM_013256.3 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:35232874 C>G maps to ENST00000392232 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr23:47836947 C>T did not map to a codon.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr23:47837102 G>T did not map to a codon.
Sequencing variant TCGA-VP-A876-01A-11D-A34U-08 chr23:47835729 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:47836865 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:27420590 G>T maps to NM_007149.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:27420266 C>T maps to NM_007149.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr3:44672663 G>A maps to NM_006991.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr3:44684196 C>T maps to NM_006991.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr19:12244345 G>A maps to NM_021143.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83H-01A-11D-A34U-08 chr11:123597403 C>A maps to NM_003455.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:123601448 G>A maps to NM_003455.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr16:3168942 G>A maps to NM_001042428.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZR-01A-11D-A41K-08 chr16:3170289 G>A maps to NM_001042428.1 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3165483 G>A maps to NM_001042428.1 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr19:22156490 C>A maps to NM_007153.3 G449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AQ-01A-11D-A33T-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A943-01A-11D-A41K-08 chr19:22154883 T>C maps to NM_007153.3 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:3190969 G>A maps to NM_001134655.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr11:6977518 C>T maps to NM_013250.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr20:52198351 C>T maps to NM_006526.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:44564708 G>A maps to NM_013361.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44635249 C>T maps to NM_013362.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44740961 C>T maps to NM_182490.1 V793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7F6-01A-11D-A33T-08 chr19:44933128 G>A maps to NM_014518.2 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr19:44515530 C>A maps to NM_006300.3 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZK-01A-11D-A41K-08 chr17:5009415 G>A maps to NM_014519.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44777925 A>G maps to NM_181756.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr18:74620422 A>G maps to NM_007345.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr18:74592172 C>A maps to NM_007345.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr18:74620342 C>T maps to NM_007345.3 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr19:24310304 A>G maps to NM_203282.2 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:116657730 C>T maps to NM_003904.3 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:3339478 C>T maps to NM_005741.4 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr16:89789104 T>A maps to NM_001113525.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:22842625 G>A maps to NM_080764.2 H366H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:44352237 C>G maps to NM_181845.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VO-01A-11D-A377-08 chr19:44891644 G>A maps to NM_152354.3 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A8WW-01A-11D-A377-08 chr17:15619874 T>G maps to NM_020652.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:18566139 G>A maps to NM_001145045.1 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:87969898 A>G maps to NM_015021.1 Q2184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr6:87966665 C>T maps to NM_015021.1 R1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr6:87969689 C>T maps to NM_015021.1 R2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr21:43412179 G>A maps to NM_020727.4 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr19:45579625 G>A maps to NM_145288.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:99669203 G>A maps to NM_032924.3 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35435318 C>T maps to NM_001099438.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OH-01A-11D-A41K-08 chr5:150276299 C>A maps to NM_001172831.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35175304 C>T maps to ENST00000221282 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LM-01A-11D-A41K-08 chr6:43323043 T>C maps to NM_014345.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr6:26637596 C>T maps to NM_024639.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:28294581 G>T maps to NM_030899.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:90487882 G>A maps to NM_182976.2 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:14829746 C>T maps to NM_032433.2 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7218-01B-11D-A32B-08 chr20:45131185 C>A maps to NM_018102.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7B4-01A-11D-A32B-08 chr20:25657356 G>A maps to NM_015655.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:25657080 C>T maps to NM_015655.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr10:38343825 T>C maps to NM_006954.1 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr8:145998962 G>A maps to NM_030580.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr20:32379197 G>T maps to ENST00000375200 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SI-01A-11D-A41K-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr5:178310628 C>T maps to NM_058230.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9N3-01A-11D-A41K-08 chr5:178310742 A>C maps to NM_058230.2 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:64159481 C>T maps to NM_014951.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr10:64136572 A>G maps to NM_199451.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:71752269 G>A maps to NM_152625.1 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:99150563 C>T maps to NM_153695.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr12:54764450 G>A maps to NM_001130967.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7509-01A-11D-A41K-08 chr3:21478534 T>G maps to NM_024697.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr7:99096408 G>A maps to NM_032164.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr8:28206325 C>T maps to NM_018660.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LZ-01A-11D-A41K-08 chr8:28218557 G>A maps to NM_018660.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr18:32843992 C>T maps to NM_001166012.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:32844159 G>A maps to NM_001166012.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:148875782 G>A maps to NM_170686.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-AB27-01A-11D-A41K-08 chr18:72589311 G>A maps to NM_017757.2 T1679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:72776114 C>T maps to NM_017757.2 I2146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:72346076 G>A maps to NM_017757.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:72775124 C>T maps to NM_017757.2 Y1816Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SK-01B-21D-A377-08 chr18:72344423 C>T maps to NM_017757.2 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:46724279 C>T maps to NM_024741.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:47307941 T>C did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:53611695 A>G maps to NM_001164309.1 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:53612553 C>T maps to NM_001164309.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:58438296 G>A maps to NM_133460.1 R418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:58005260 C>T maps to NM_001098491.1 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr16:49669906 C>T maps to NM_015069.2 A1052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:21719313 C>A maps to NM_001001415.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:22001954 T>G maps to NM_003423.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr19:12126895 T>C maps to NM_001080411.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr16:3440103 T>A maps to ENST00000396852 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:12540984 A>G maps to NM_005815.4 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A7FA-01A-21D-A33T-08 chr3:44488285 G>A maps to NM_181489.5 C959C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:44418987 G>T maps to NM_003425.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:178391869 C>T maps to NM_182594.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:178392865 G>A maps to NM_182594.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SB-01A-31D-A377-08 chr5:178392553 T>G maps to NM_182594.2 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr9:109701287 C>G maps to NM_021224.4 A2109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:149462732 G>A maps to NM_207336.1 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QX-01A-11D-A377-08 chr19:53344799 G>A maps to NM_001008801.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A720-01A-12D-A32B-08 chr16:30409410 C>T maps to ENST00000495929 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9OQ-01A-11D-A41K-08 chr16:30410426 G>T maps to ENST00000495929 *748L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr9:95609133 A>G maps to NM_031486.1 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr10:44104059 A>T did not map to a codon.
Sequencing variant TCGA-KC-A7FD-01A-11D-A33T-08 chr10:48370747 G>A maps to NM_153034.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9KY-01A-11D-A41K-08 chr19:22846974 C>A maps to NM_020855.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:58867510 C>T maps to NM_198458.1 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr9:99521386 G>A maps to NM_014930.1 N575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr2:27822523 C>T maps to NM_032434.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:74091249 G>A maps to ENST00000443185 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:74091237 C>T maps to ENST00000443185 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:74091285 G>A maps to ENST00000443185 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:74153282 G>A maps to ENST00000443185 A576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HO-01A-11D-A364-08 chr18:74091975 T>A maps to ENST00000443185 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:97916525 A>G maps to NM_014803.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr4:10445819 G>A maps to NM_053042.2 N711N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr4:10447769 T>A maps to NM_053042.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88P-01A-11D-A34U-08 chr4:10447286 G>C maps to NM_053042.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr18:14104993 A>C maps to NM_145287.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr18:22804680 G>A maps to NM_015461.2 C1067C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr18:22807245 C>T maps to NM_015461.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:42729172 C>T maps to NM_133444.1 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:52937266 G>A maps to NM_001143939.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:30935326 C>T maps to NM_014717.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr19:30935518 C>T maps to NM_014717.1 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A8CY-01A-11D-A364-08 chr19:30935473 C>T maps to NM_014717.1 N335N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:30935422 C>T maps to NM_014717.1 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:31039261 G>A maps to NM_014717.1 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S8-01A-11D-A377-08 chr19:30935383 C>T maps to NM_014717.1 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:57910578 G>A maps to NM_001172773.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:58198230 C>T maps to ENST00000356715 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WJ-01A-11D-A377-08 chr19:2833763 A>T maps to NM_001102651.1 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XQ-A8TA-01A-11D-A364-08 chr19:2877441 G>A maps to NM_024967.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:7075114 C>T maps to NM_024341.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr19:9453236 A>G maps to NM_032497.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:12638261 A>C maps to NM_144976.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2917986 C>A maps to NM_173480.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr19:38056279 C>T maps to NM_016536.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr8:125989772 C>T maps to NM_152412.2 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:42585298 G>A maps to ENST00000222339 Q937Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr19:44103388 G>A maps to NM_024327.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr19:44103049 T>C maps to NM_024327.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr19:52376324 G>C maps to NM_032679.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:56090150 C>T maps to NM_152600.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WK-01A-11D-A377-08 chr19:58288002 G>A maps to NM_017652.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:58370782 C>T maps to NM_032828.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:58371213 C>T maps to NM_032828.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr15:85326136 G>A maps to NM_014630.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:5085328 G>T maps to NM_032530.1 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:3487539 T>G did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2049980 C>T maps to ENST00000431526 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:2050145 C>T maps to ENST00000431526 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:53270591 A>C maps to NM_198457.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8I9-01A-11D-A364-08 chr19:58499975 G>A maps to NM_025027.3 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:38190089 G>A maps to NM_032689.4 C314C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:123984771 C>A maps to NM_020747.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr5:123983469 C>T maps to NM_020747.2 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr15:64967479 C>T maps to NM_015042.1 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr19:52496291 C>T maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:52619033 G>A maps to NM_178523.3 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:52619168 C>T maps to NM_178523.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:16465317 T>A maps to NM_033414.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr19:55994209 G>A maps to NM_033113.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30794559 C>T maps to NM_001080417.1 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr2:71577013 C>T maps to NM_014497.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:48737262 C>A maps to NM_152320.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr12:48741843 C>T maps to NM_152320.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:91406184 C>T maps to NM_201269.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:22291616 G>A did not map to a codon.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr16:31090752 C>T maps to NM_014699.3 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AU-01A-11D-A32B-08 chr1:182025560 C>A maps to NM_001009992.1 E529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:182027060 G>A maps to NM_001009992.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr3:44636459 C>T maps to NM_173658.1 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L1-01A-11D-A41K-08 chr3:42956593 G>A maps to NM_001134656.1 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:53668563 C>T maps to NM_024733.3 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YJ-A8SW-01A-11D-A377-08 chr19:53668834 G>C maps to NM_024733.3 S303*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XK-AAIW-01A-11D-A41K-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:31073036 C>T maps to ENST00000417110 D75D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-YL-A8SF-01A-11D-A377-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZG-A9L4-01A-11D-A41K-08 chr19:58232391 G>A maps to ENST00000335820 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr1:227842074 C>T maps to NM_178549.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr7:63709525 C>T maps to NM_153363.2 R11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr1:26691328 C>A maps to ENST00000436292 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83J-01A-11D-A364-08 chr16:30581272 G>A maps to NM_145271.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:30620888 A>C maps to NM_138447.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9L0-01A-11D-A41K-08 chr1:247150484 A>C maps to NM_020394.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A6RA-01A-11D-A33T-08 chr22:24086055 G>A maps to NM_021916.2 C424C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A878-01A-31D-A34U-08 chr22:24086388 G>A maps to NM_021916.2 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:24086193 C>T maps to NM_021916.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:12060641 C>T maps to NM_144566.1 F601F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88M-01A-11D-A34U-08 chr19:12060806 A>G maps to NM_144566.1 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:12575379 C>T maps to ENST00000428311 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAJP-01A-11D-A41K-08 chr19:12575379 C>T maps to ENST00000428311 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87C-01A-11D-A34U-08 chr19:57133479 C>T maps to NM_021216.4 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-A9S7-01A-11D-A41K-08 chr15:90610701 C>T maps to NM_198526.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8II-01A-11D-A364-08 chr23:84526038 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:20728102 C>T maps to NM_001159293.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SA-01A-21D-A377-08 chr19:20728084 G>A maps to NM_001159293.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:149174838 C>T maps to NM_001163474.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8W3-01A-11D-A377-08 chr17:80790120 T>G maps to NM_024702.2 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:80788497 C>T maps to NM_024702.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V1-A9ZG-01A-11D-A41K-08 chr17:80789373 G>A maps to NM_024702.2 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr23:134427899 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr6:35261619 T>C maps to NM_003427.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr19:53958819 T>C maps to NM_001008401.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:53958864 C>A maps to NM_001008401.3 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:12089671 C>A maps to NM_001012753.1 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:52793388 G>A maps to NM_001010851.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30536158 G>A maps to NM_024671.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:2933819 G>T maps to NM_021217.2 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr19:2934176 C>T maps to NM_021217.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:149133689 G>A maps to ENST00000440594 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:149129127 C>T maps to ENST00000440594 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:89294898 G>T maps to NM_182531.2 G707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr19:40580581 C>T maps to NM_001142577.1 E590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr19:40540947 A>G maps to NM_001005851.2 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:38160482 G>A maps to NM_152605.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:99581088 T>A maps to NM_001001662.1 K406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:30594699 C>T maps to NM_152458.6 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8HM-01A-11D-A364-08 chr7:148768339 C>T maps to NM_152411.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:56600279 C>T maps to NM_001002836.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:130198256 C>T maps to NM_007135.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:35449063 G>A maps to NM_175872.4 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:38028573 G>A maps to NM_001013659.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:12501648 T>A maps to NM_001080821.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CL-01A-11D-A34U-08 chr2:185802144 T>A maps to NM_194250.1 C674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-TP-A8TT-01A-12D-A41K-08 chr2:185803617 T>G maps to NM_194250.1 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr23:47774322 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:146824229 G>A maps to ENST00000508784 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:146823319 G>C maps to ENST00000508784 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WI-01A-11D-A377-08 chr4:146700586 G>A maps to ENST00000508784 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:115090480 G>A maps to NM_032436.2 E388E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A8QW-01A-11D-A377-08 chr19:53117663 A>G maps to NM_018300.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88O-01A-11D-A34U-08 chr17:33289178 G>T maps to NM_052857.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr20:57769547 G>A maps to NM_178457.1 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:57829413 A>T maps to NM_178457.1 G1550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:57175471 G>A maps to NM_001005850.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:57175885 G>A maps to NM_001005850.1 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XJ-A83F-01A-11D-A34U-08 chr19:57175801 G>A maps to NM_001005850.1 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:57175978 G>A maps to NM_001005850.1 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:57176449 G>A maps to NM_001005850.1 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SO-01B-31D-A377-08 chr19:52658799 A>G maps to NM_001102657.1 Y712Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr14:102798053 C>T maps to NM_018335.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZG-A9LU-01A-11D-A41K-08 chr19:52569154 T>C maps to NM_001136499.1 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:53854687 C>T maps to NM_138374.1 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:149558855 C>T maps to NM_001099220.1 N869N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr19:12155152 G>T maps to NM_001080404.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIV-01A-11D-A41K-08 chr19:12155834 G>A maps to NM_001080404.1 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:52887681 T>A maps to NM_001145434.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr19:23543400 C>A maps to NM_003430.2 G794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:23543821 A>G maps to NM_003430.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A8CN-01A-11D-A34U-08 chr19:23544859 T>A maps to NM_003430.2 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:64864736 C>T maps to NM_152626.2 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2A-A8VV-01A-11D-A377-08 chr19:22940379 T>C maps to ENST00000397104 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr19:22951197 G>A maps to ENST00000397104 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A7AY-01A-11D-A33T-08 chr19:22939395 A>G maps to ENST00000397104 F925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88I-01A-11D-A34U-08 chr19:22940631 C>T maps to ENST00000397104 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VP-A87K-01A-11D-A34U-08 chr19:22940574 T>C maps to ENST00000397104 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:22939741 A>G maps to ENST00000397104 C863C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:47864561 G>A maps to NM_021035.2 L1667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr7:30395398 G>A maps to NM_147128.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr22:29444420 C>T maps to NM_032173.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A9WH-01A-11D-A377-08 chr22:29438480 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:5456786 C>T maps to NM_181710.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr19:5455561 G>A maps to NM_181710.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:60640727 C>T maps to NM_207341.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr11:60643127 G>A maps to NM_207341.2 *639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:21210893 G>A maps to NM_003460.1 R642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:238048880 C>T did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:238053224 C>T maps to NM_021186.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A7NM-01A-21D-A33T-08 chr3:102171847 G>A maps to NM_175056.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A8IB-01A-11D-A364-08 chr10:126672052 A>G maps to NM_017580.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8S9-01A-11D-A377-08 chr10:126662250 A>G maps to NM_017580.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:71536661 G>A maps to NM_203350.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M7-A725-01A-12D-A32B-08 chr2:135965228 C>T maps to NM_032143.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr23:15809136 G>T did not map to a codon.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:58565059 C>A maps to NM_182572.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr16:3140144 G>A maps to NM_032805.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A83K-01A-11D-A34U-08 chr6:28097611 C>T maps to NM_025231.1 Q311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr15:85164526 C>T maps to NM_181877.3 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YL-A8SH-01B-11D-A377-08 chr15:85164526 C>T maps to NM_181877.3 C367C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KK-A7AQ-01A-11D-A33T-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr15:43654115 C>A maps to NM_152455.3 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VN-A88Q-01A-11D-A34U-08 chr19:58187584 G>A maps to NM_152677.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:56733189 G>A maps to NM_024303.1 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:56701609 G>A maps to NM_001080456.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr20:44505964 G>A maps to NM_080752.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr19:13923940 C>T maps to NM_023072.2 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:45484151 G>A maps to NM_020883.1 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:45484893 G>A maps to NM_020883.1 H930H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:66821853 G>A maps to NM_017975.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr10:58119552 G>A maps to NM_032997.2 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr23:57619096 G>A did not map to a codon.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:53261993 G>A maps to NM_024646.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr7:143085618 G>A maps to NM_001010972.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr17:3992019 C>T maps to NM_015113.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr17:3979977 C>A maps to NM_015113.3 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr17:3959635 T>C maps to NM_015113.3 Q1723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr17:4007993 C>T maps to NM_015113.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XK-AAIW-01A-11D-A41K-08 chr1:78098876 C>A maps to NM_015534.4 E55*. Only missense variants will be evaluated by CHASM.
